Konjenital Enfeksiyonların ve Koronavirüs Hastalığı-2019 (Covid-9) Enfeksiyonunun

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Referanslar

Adamo, P., Asís, L., Silveyra, P., Cuffini, C., Pedranti, M. & Zapata, M. (2004). Rubella virus does not ınduce apoptosis in primary human embryo fibroblast cultures: A possible way of viral persistence in congenital Infection. Viral Immunology, 17(1), 87–100.

Al-awaidy, S., Griffiths, U.K., Mohammed, H., Bawikar, S., Al-aisiri, M. S., Khandekar, R. & Robertson, S.E. (2006). Costs of congenital rubella syndrome (CRS) in Oman : Evidence based on long-term follow-up of 43 children. Vaccine, 24, 6437–6445.

Al-haddad, B.J.S., Oler, E., Armistead, B., Elsayed, N.A., Weinberger, D.R., Bernier, R. & … Waldorf, K.M.A. (2020). The fetal origins of mental illness. Am J Obstet Gynecol, 221(6), 549–562.

Allotey, J., Chatterjee, S., Kew, T., Gaetano, A., Stallings, E., Fernández-garcía, S. & … Thangaratinam, S. (2022). SARS-CoV-2 positivity in offspring and timing of mother-to-child transmission : living systematic review and meta-analysis. BMJ, 376, 1–11.

Andersen R. D. (1987). Herpes simplex virus infection of the neonatal respiratory tract. American journal of diseases of children (1960), 141(3), 274–276. https://doi.org/10.1001/archpedi.1987.04460030052023

Angelone, D.F., Wessels, M.R., Coughlin, M., Suter, E.E., Valentini, P., Kalish, L.A. &… Boston, H. (2006). Innate ımmunity of the human newborn is polarized toward a high ratio of IL-6/TNF- alpha production in vitro and in vivo. Pediatr Res, 60(2), 205–209. https://doi.org/10.1203/01.pdr.0000228319.10481.ea

Ashary, N., Bhide, A., Chakraborty, P. & Colaco, S. (2020). Single- Cell RNA -seq identifies cell subsets in human placenta that highly expresses factors driving pathogenesis of SARS-CoV-2. Front Cell Dev Biol, 8, 1–16. https://doi.org/10.3389/fcell.2020.00783

Atladóttir, H. O., Thorsen, P., Østergaard, L., Schendel, D. E., Lemcke, S., Abdallah, M., & Parner, E. T. (2010). Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. Journal of autism and developmental disorders, 40(12), 1423–1430. https://doi.org/10.1007/s10803-010-1006-y

Ayed, M., Embaireeg, A., Kartam, M., More, K., Alqallaf, M., Alnafisi, A., Fouzan, W.A. & Hessa Alkandari. (2022). Neurodevelopmental outcomes of infants born to mothers with SARS‑CoV‑2 infections during pregnancy: A national prospective study in Kuwait. BMC Pediatrics, 22, 1–11. https://doi.org/10.1186/s12887-022-03359-2

Bale, J.F. (2009). Fetal infections and brain development. Clin Perinatol, 36, 639–653. https://doi.org/10.1016/j.clp.2009.06.005

Balistreri, W. F. & Journal, T. (2008). When Should You Initiate Acyclovir Therapy in a Neonate? J Pediatr, 153(2), 155-6. doi: 10.1016/j.jpeds.2008.04.027.

Banatvala, J.E. & Brown, D.W.G. (2004). Rubella. Lancet, 363(9415), 1127-1137. doi: 10.1016/S0140-6736(04)15897-2.

Barry, H. & Barry, H. (1961). Season of Birth, Archives of General Psychiatry, 5, 292–300.

Baud, O., Fontaine, R. H., Olivier, P., Maury, L., Moussawi, F. E., Bauvin, I. & Aujard, Y. (2007). Premature rupture of membranes: pathophysiology of neurological impact. Archives de pediatrie, 14, 49-53.

Bennett, S. & Nagler, J. (2014). Images in emergency medicine. Herpes simplex virus encephalitis. Ann Emerg Med, 64(6):588, 608.

Bertero, L., Borella, F., Botta, G., Carosso, A., Cosma, S., Bovetti, M. & Benedetto, C. (2021). Placenta histopathology in SARS-CoV-2 infection: analysis of a consecutive series and comparison with control cohorts, Virchows Arch, 479(4):715-728. doi: 10.1007/s00428-021-03097-3.

Boksa, P. (2010). Brain , Behavior , and Immunity Effects of prenatal infection on brain development and behavior: A review of findings from animal models. Brain Behav Immun, 24(6):881-97. doi: 10.1016/j.bbi.2010.03.005.

Bonthius, D. J., Nichols, B., Harb, H. & Mahoney, J. (2007). Lymphocytic Choriomeningitis Virus Infection of the Developing Brain: Critical Role of Host Age. Ann Neurol, 62(4):356-374. doi:10.1002/ana.21193.

Boudaouara, Y., Aoun, K., Maatoug, R., Souissi, O. & Abdallah, R. Ben. (2018). Congenital Toxoplasmosis in Tunisia: Prenatal and Neonatal Diagnosis and Postnatal Follow-up of 35 Cases. Am J Trop Med Hyg, 98(6), 1722–1726. https://doi.org/10.4269/ajtmh.17-0580

Brown, A.S., Schaefer, C.A., Wyatt, R.J., Qoetz, R., Begg, M.D., Qorman, J.M. & Susser, E. S. (1996). Maternal Exposure to Respiratory Infections and Adult Schizophrenia Spectrum Disorders: A Prospective Birth Cohort Study. Schizophr Bull, 26(2), 287–296

Brown, Z. A., Benedetti, J., Ashley, R., Burchett, S., Selke, S., Berry, S., Vontver, L. A., & Corey, L. (1991). Neonatal herpes simplex virus infection in relation to asymptomatic maternal infection at the time of labor. The New England journal of medicine, 324(18), 1247–1252. https://doi.org/10.1056/NEJM199105023241804

Burd, I., Balakrishnan, B. & Kannan, S. (2012). Models of fetal brain injury, intrauterine inflammation , and Preterm Birth. Am J Reprod Immunol, 67(4), 287–295. https://doi.org/10.1111/j.1600-0897.2012.01110.x

Callaghan, E.O., Sham, P.C., Takei, N., Murray, G., Glover, G., Hare, E.H. & Murray, R.M. (1994). The Relationship of Schizophrenic Births to 16 Infectious Diseases. Br J Psychiatry, 165(3), 353–356.

Carson, M.J., Doose, J.M., Melchior, B., Schmid, C.D. & Ploix, C.C. (2009). CNS immune privilege : hiding in plain sight. Immunol Rev, 213, 48–65. https://doi.org/10.1111/j.1600-065X.2006.00441.x.CNS

Caviness, A. C., Demmler, G. J., Almendarez, Y., & Selwyn, B. J. (2008). The prevalence of neonatal herpes simplex virus infection compared with serious bacterial illness in hospitalized neonates. The Journal of pediatrics, 153(2), 164–169. https://doi.org/10.1016/j.jpeds.2008.02.031

Cheeran, M.C., Lokensgard, J.R. & Schleiss, M.R. (2009). Neuropathogenesis of Congenital Cytomegalovirus Infection: Disease Mechanisms and Prospects for Intervention. Clin Microbiol Rev, 22(1), 99–126. https://doi.org/10.1128/CMR.00023-08

Cluver, C., Meyer, R., Odendaal, H. & Geerts, L. (2013). Congenital rubella with agenesis of the inferior cerebellar vermis and total anomalous pulmonary venous drainage. Ultrasound Obstet Gynecol, 42(2), 235–237. https://doi.org/10.1002/uog.12399

Cooper, L.Z. (1985). The History and Medical Consequences of Rubella. Rev Infect Dis, 7, 2-10. doi: 10.1093/clinids/7.supplement_1.s2.

Corey, L., Whitley, R. J., Stone, E. F., & Mohan, K. (1988). Difference between herpes simplex virus type 1 and type 2 neonatal encephalitis in neurological outcome. Lancet (London, England), 1(8575-6), 1–4. https://doi.org/10.1016/s0140-6736(88)90997-x

Cradock-watson, J.E. & Pollock, T.M. (1982). Consequences of confirmed maternal rubella at successive stages of pregnancy. Lancet, 2(8302), 781-784. doi: 10.1016/s0140-6736(82)92677-0.

Desmond, M.M., Wilson, G.S., Vorderman, A.L., Murphy, M.A., Fisher, E.S. & Kroulik, E.M. (1967). The health and educational status of adolescents with congenital rubella syndrome. Dev Med Child Neurol, 27(6),721-729. doi: 10.1111/j.1469-8749.1985.tb03795.x.

Desmonts, G. & Couvreur, J. (1974). Congenital toxoplasmosis. A prospective study of 378 pregnancies. N Engl J Med, 290(20), 1110-1116. doi: 10.1056/NEJM197405162902003

Dudgeon J. A. (1975). Congenital rubella. The Journal of pediatrics, 87(6 Pt 2), 1078–1086. https://doi.org/10.1016/s0022-3476(75)80119-3

Duncan, R., Muller, J., Lee, N., Esmaili, A. & Nakhasi, H.L. (1999). Rubella Virus-Induced Apoptosis Varies among Cell Lines and Is Modulated by Bcl-X L and Caspase Inhibitors. Virology, 255(1), 117–128.

Durukan, D., Fairley, C.K., Bradshaw, C.S., Read, T.R.H., Druce, J., Catton, M. & Chow, E. P.F. (2018). Increasing proportion of herpes simplex virus type 1 among women and men diagnosed with first-episode anogenital herpes: A retrospective observational study over 14 years in Melbourne , Australia, Sex Transm Infect, 95(4), 307-313. https://doi.org/10.1136/sextrans-2018-053830

Edlow, A.G., Castro, V.M., Shook, L.L., Kaimal, A.J. & Perlis, R.H. (2022). Neurodevelopmental Outcomes at 1 Year in Infants of Mothers Who Tested Positive for SARS-CoV-2 During Pregnancy, JAMA Netw Open, 5(6), 1–10. https://doi.org/10.1001/jamanetworkopen.2022.15787

Engert, V., Siauw, C., Stock, A., Rehn, M., Wöckel, A., Härtel, C. & Wirbelauer, J. (2021). Severe Brain Damage in a Moderate Preterm Infant as Complication of Post-COVID-19 Response during Pregnancy. Neonatology, 118(4), 505-508. https://doi.org/10.1159/000516846

Esiri M. M. (1982). Herpes simplex encephalitis. An immunohistological study of the distribution of viral antigen within the brain. Journal of the neurological sciences, 54(2), 209–226. https://doi.org/10.1016/0022-510x(82)90183-6

Estato, V., Stipursky, J., Gomes, F., Mergener, T.C., Frazão-teixeira, E., Allodi, S. & Adesse, D. (2018). The Neurotropic Parasite Toxoplasma gondii Induces Sustained Neuroin fl ammation with Microvascular Dysfunction in Infected Mice. The American Journal of Pathology, 188(11), 2674–2687. https://doi.org/10.1016/j.ajpath.2018.07.007

Fernandes, A. F., Lange, M. C., Novak, F. T., Zavala, J. A., Zamproni, L. N., Germiniani, F. M., Piovesan, E. J., & Teive, H. A. (2010). Extra-temporal involvement in herpes simplex encephalitis. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 17(9), 1221–1223 https://doi.org/10.1016/j.jocn.2010.02.007

French, R. R., & York, D. A. (1984). The regulation of adenylate cyclase in adipocyte plasma membrane from genetically obese (ob/ob) mice. Diabetologia, 26(6), 466–472. https://doi.org/10.1007/BF00262223

Gabrielli, L., Bonasoni, M. P., Santini, D., Piccirilli, G., Chiereghin, A., Petrisli, E. & Piccioli, M. (2012). Congenital cytomegalovirus infection: patterns of fetal brain damage. Clin Microbiol Infect, 18(10), 419-427.

Gan, X., Zhang, X., Cheng, Z., Chen, L., Ding, X., Du, J. & Yu, L. (2016). Toxoplasma gondii inhibits differentiation of C17.2 neural stem cells through Wnt/β-catenin signaling pathway. Biochem Biophys Res Commun, 473(1), 187-193. https://doi.org/10.1016/j.bbrc.2016.03.076

Germano, C., Messina, A., Tavella, E., Vitale, R., Avellis, V., Barboni, M., Attini, R., Revelli, A., Zola, P., Manzoni, P., & Masturzo, B. (2022). Fetal Brain Damage during Maternal COVID-19: Emerging Hypothesis, Mechanism, and Possible Mitigation through Maternal-Targeted Nutritional Supplementation. Nutrients, 14(16), 3303. https://doi.org/10.3390/nu14163303

Gordon-lipkin, E., Hoon, A. & Pardo, C.A. (2022). Prenatal cytomegalovirus, rubella, and Zika virus infections associated with developmental disabilities: past, present, and future. Dev Med Child Neurol, 63(2), 135–143. https://doi.org/10.1111/dmcn.14682.Prenatal

Gordon-Lipkin, E., & Peacock, G. (2019). The Spectrum of Developmental Disability with Zika Exposure: What Is Known, What Is Unknown, and Implications for Clinicians. Journal of developmental and behavioral pediatrics: JDBP, 40(5), 387–395. https://doi.org/10.1097/DBP.0000000000000665

Gordon, B. & Neilson, M. (1975). Mental disorder and season of birth--a southern hemisphere study. Br J Psychiatry, 129, 355–361.

Gregg, N. M. & Banatvala, R. J. E. (2001). Congenital cataract following German measles in the mother. 1941. Aust N Z J Ophthalmol, 19(4), 267-76.

Hecht, J. L., Quade, B., Deshpande, V., David, M. M., Desai, N., Dygulska, B., Bates, S.V. & Roberts, D.J. (2020). SARS-CoV-2 can infect the placenta and is not associated with specific placental histopathology: a series of 19 placentas from COVID-19-positive mothers. Mod Pathol, 33(11), 2092-2103.

Hermes, G., Ajioka, J. W., Kelly, K. A., Mui, E., Roberts, F., Kasza, K., Mayr, T., Kirisits, M. J., Wollmann, R., Ferguson, D. J., Roberts, C. W., Hwang, J. H., Trendler, T., Kennan, R. P., Suzuki, Y., Reardon, C., Hickey, W. F., Chen, L., & McLeod, R. (2008). Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection. Journal of neuroinflammation, 5, 48. https://doi.org/10.1186/1742-2094-5-48

Huang, P., Zhou, F., Guo, Y., Yuan, S., Lin, S., Lu, J., Tu, S., Lu, M., Shen, S., Guedeney, A., Xia, H., & Qiu, X. (2021). Association Between the COVID-19 Pandemic and Infant Neurodevelopment: A Comparison Before and During COVID-19. Frontiers in pediatrics, 9, 662165. https://doi.org/10.3389/fped.2021.662165

Hudson, S. J., Dix, R. D., & Streilein, J. W. (1991). Induction of encephalitis in SJL mice by intranasal infection with herpes simplex virus type 1: a possible model of herpes simplex encephalitis in humans. The Journal of infectious diseases, 163(4), 720–727. https://doi.org/10.1093/infdis/163.4.720

Huleihel, M., Golan, H., & Hallak, M. (2004). Intrauterine infection/inflammation during pregnancy and offspring brain damages: possible mechanisms involved. Reproductive biology and endocrinology, 2, 17. https://doi.org/10.1186/1477-7827-2-17

Istas, A. S., Demmler, G. J., Dobbins, J. G., & Stewart, J. A. (1995). Surveillance for congenital cytomegalovirus disease: a report from the National Congenital Cytomegalovirus Disease Registry. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 20(3), 665–670. https://doi.org/10.1093/clinids/20.3.665

Jamieson, D. J., Ellis, J. E., Jernigan, D. B., & Treadwell, T. A. (2006). Emerging infectious disease outbreaks: old lessons and new challenges for obstetrician-gynecologists. American journal of obstetrics and gynecology, 194(6), 1546–1555. https://doi.org/10.1016/j.ajog.2005.06.062

Long S. S. (2008). In defense of empiric acyclovir therapy in certain neonates. The Journal of pediatrics, 153(2), 157–158. https://doi.org/10.1016/j.jpeds.2008.04.071

Kimberlin D.W. (2004). Neonatal herpes simplex infection. Clinical microbiology reviews, 17(1), 1–13. https://doi.org/10.1128/CMR.17.1.1-13.2004

Koch, L. H., Fisher, R. G., Chen, C., Foster, M. M., Bass, W. T., & Williams, J. V. (2009). Congenital herpes simplex virus infection: two unique cutaneous presentations associated with probable intrauterine transmission. Journal of the American Academy of Dermatology, 60(2), 312–315. https://doi.org/10.1016/j.jaad.2008.08.038

Lazarte-Rantes, C., Rodríguez-Anccasi, R., Rivas-Campos, C., & Silva, E. (2021). Congenital Toxoplasmosis: Findings in Fetal MRI. Cureus, 13(8), e16894. https://doi.org/10.7759/cureus.16894

Leas, B. F., & Umscheid, C. A. (2015). Neonatal Herpes Simplex Virus Type 1 Infection and Jewish Ritual Circumcision With Oral Suction: A Systematic Review. Journal of the Pediatric Infectious Diseases Society, 4(2), 126–131. https://doi.org/10.1093/jpids/piu075

Lee, B. K., Magnusson, C., Gardner, R. M., Blomström, Å., Newschaffer, C. J., Burstyn, I., Karlsson, H., & Dalman, C. (2015). Maternal hospitalization with infection during pregnancy and risk of autism spectrum disorders. Brain, behavior, and immunity, 44, 100–105. https://doi.org/10.1016/j.bbi.2014.09.001

Lee, J. Y., & Bowden, D. S. (2000). Rubella virus replication and links to teratogenicity. Clinical microbiology reviews, 13(4), 571–587. https://doi.org/10.1128/CMR.13.4.571

Littauer, E. Q., Esser, E. S., Antao, O. Q., Vassilieva, E. V., Compans, R. W., & Skountzou, I. (2017). H1N1 influenza virus infection results in adverse pregnancy outcomes by disrupting tissue-specific hormonal regulation. PLoS pathogens, 13(11), e1006757. https://doi.org/10.1371/journal.ppat.1006757

Louie, J. K., Shaikh-Laskos, R., Preas, C., Nguyen, V. T., Peters, A., & Messenger, S. (2009). Re-emergence of another vaccine-preventable disease?-Two cases of rubella in older adults. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 46(1), 98–100. https://doi.org/10.1016/j.jcv.2009.06.013

Malik, A. N., Hildebrand, G. D., Sekhri, R., & Russell-Eggitt, I. M. (2008). Bilateral macular scars following intrauterine herpes simplex virus type 2 infection. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 12(3), 305–306. https://doi.org/10.1016/j.jaapos.2008.01.002

Marquez, L., Levy, M. L., Munoz, F. M., & Palazzi, D. L. (2011). A report of three cases and review of intrauterine herpes simplex virus infection. The Pediatric infectious disease journal, 30(2), 153–157. https://doi.org/10.1097/INF.0b013e3181f55a5c

Marcos, A. C., Siqueira, M., Alvarez-Rosa, L., Cascabulho, C. M., Waghabi, M. C., Barbosa, H. S., Adesse, D., & Stipursky, J. (2020). Toxoplasma gondii infection impairs radial glia differentiation and its potential to modulate brain microvascular endothelial cell function in the cerebral cortex. Microvascular research, 131, 104024. https://doi.org/10.1016/j.mvr.2020.104024

Meaney-Delman, D., Jamieson, D. J., & Rasmussen, S. A. (2017). Addressing the effects of established and emerging infections during pregnancy. Birth defects research, 109(5), 307–310. https://doi.org/10.1002/bdr2.1018

Mednick, S. A., Machon, R. A., Huttunen, M. O., & Bonett, D. (1988). Adult schizophrenia following prenatal exposure to an influenza epidemic. Archives of general psychiatry, 45(2), 189–192. https://doi.org/10.1001/archpsyc.1988.01800260109013

Melvin, A. J., Mohan, K. M., Vora, S. B., Selke, S., Sullivan, E., & Wald, A. (2022). Neonatal Herpes Simplex Virus Infection: Epidemiology and Outcomes in the Modern Era. Journal of the Pediatric Infectious Diseases Society, 11(3), 94–101. https://doi.org/10.1093/jpids/piab105

Nguyen, T. Van, Pham, V. H., & Abe, K. (2015). EBioMedicine Pathogenesis of Congenital Rubella Virus Infection in Human Fetuses : Viral Infection in the Ciliary Body Could Play an Important Role in Cataractogenesis. EBIOM, 2(1), 59–63. https://doi.org/10.1016/j.ebiom.2014.10.021

Orenstein, W. A., Bart, K. J., Hinman, A. R., Preblud, S. R., Greaves, W. L., Doster, S. W., Stetler, H. C., & Sirotkin, B. (1984). The opportunity and obligation to eliminate rubella from the United States. JAMA, 251(15), 1988–1994.

Palmer, C., Towfighi, J., Roberts, R. L., & Heitjan, D. F. (1993). Allopurinol administered after inducing hypoxia-ischemia reduces brain injury in 7-day-old rats. Pediatric research, 33(4 Pt 1), 405–411. https://doi.org/10.1203/00006450-199304000-00018

Pappas, G., Roussos, N., & Falagas, M. E. (2009). Toxoplasmosis snapshots : Global status of Toxoplasma gondii seroprevalence and implications for pregnancy and congenital toxoplasmosis. International Journal for Parasitology, 39(12), 1385–1394. https://doi.org/10.1016/j.ijpara.2009.04.003

Parisot, S., Droulle, P., Feldmann, M., Pinaud, P., & Marchal, C. (1991). Unusual encephaloclastic lesions with paraventricular calcification in congenital rubella. Pediatric radiology, 21(3), 229–230. https://doi.org/10.1007/BF02011057

Park, C., Moon, K. C., Park, J. S., Jun, J. K., & Yoon, B. H. (2009). The Frequency and Clinical Significance of Intra-Uterine Infection and Inflammation in Patients with Placenta Previa and Preterm Labor and Intact Membranes. Placenta, 30(7), 613–618. https://doi.org/10.1016/j.placenta.2009.04.005

Petito, C. K., Torres-Muñoz, J. E., Zielger, F., & McCarthy, M. (2006). Brain CD8+ and cytotoxic T lymphocytes are associated with, and may be specific for, human immunodeficiency virus type 1 encephalitis in patients with acquired immunodeficiency syndrome. Journal of neurovirology, 12(4), 272–283. https://doi.org/10.1080/13550280600879204

Plotkin S. A. (2006). The history of rubella and rubella vaccination leading to elimination. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 43 Suppl 3, S164–S168. https://doi.org/10.1086/505950

Prabhu, M., & Riley, L. E. (2023). Coronavirus Disease 2019 (COVID-19) Vaccination in Pregnancy. Obstetrics and gynecology, 141(3), 473–482. https://doi.org/10.1097/AOG.0000000000005100

Ramiro-Cortijo, D., de la Calle, M., Böger, R., Hannemann, J., Lüneburg, N., López-Giménez, M. R., Rodríguez-Rodríguez, P., Martín-Cabrejas, M. Á., Benítez, V., de Pablo, Á. L. L., González, M. D. C., & Arribas, S. M. (2020). Male fetal sex is associated with low maternal plasma anti-inflammatory cytokine profile in the first trimester of healthy pregnancies. Cytokine, 136, 155290. https://doi.org/10.1016/j.cyto.2020.155290

Raony, Í., de Figueiredo, C. S., Pandolfo, P., Giestal-de-Araujo, E., Oliveira-Silva Bomfim, P., & Savino, W. (2020). Psycho-Neuroendocrine-Immune Interactions in COVID-19: Potential Impacts on Mental Health. Frontiers in immunology, 11, 1170. https://doi.org/10.3389/fimmu.2020.01170

Reef, S. E., Redd, S. B., Abernathy, E., Zimmerman, L., & Icenogle, J. P. (2006). The epidemiological profile of rubella and congenital rubella syndrome in the United States, 1998-2004: the evidence for absence of endemic transmission. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 43 Suppl 3, S126–S132. https://doi.org/10.1086/505944

Rorke, L. B., & Spiro, A. J. (1967). Cerebral lesions in congenital rubella syndrome. The Journal of pediatrics, 70(2), 243–255. https://doi.org/10.1016/s0022-3476(67)80419-0

Saito, K., Packianathan, S., & Longo, L. D. (1997). Free radical-induced elevation of ornithine decarboxylase activity in developing rat brain slices. Brain research, 763(2), 232–238. https://doi.org/10.1016/s0006-8993(97)00414-9

Saxon, S. A., Knight, W., Reynolds, D. W., Stagno, S., & Alford, C. A. (1973). Intellectual deficits in children born with subclinical congenital toxoplasmosis: a preliminary report. The Journal of pediatrics, 82(5), 792–797. https://doi.org/10.1016/s0022-3476(73)80068-x

Seckl, J. R., & Holmes, M. C. (2007). Mechanisms of disease: glucocorticoids, their placental metabolism and fetal 'programming' of adult pathophysiology. Nature clinical practice. Endocrinology & metabolism, 3(6), 479–488. https://doi.org/10.1038/ncpendmet0515

Shanes, E. D., Mithal, L. B., Otero, S., Azad, H. A., Miller, E. S., & Goldstein, J. A. (2020). Placental Pathology in COVID-19. American journal of clinical pathology, 154(1), 23–32. https://doi.org/10.1093/ajcp/aqaa089

Sheinbergas, M.M. (1976). Hydrocephalus due to Prenatal Infection with the Lymphocytic Choriomeningitis Virus. Infection, 4(4), 185–191

Shook, L. L., & Edlow, A. G. (2023). Safety and Efficacy of Coronavirus Disease 2019 (COVID-19) mRNA Vaccines During Lactation. Obstetrics and gynecology, 141(3), 483–491. https://doi.org/10.1097/AOG.0000000000005093

Simard, A. R., & Rivest, S. (2005). Do pathogen exposure and innate immunity cause brain diseases?. Neurological research, 27(7), 717–725. https://doi.org/10.1179/016164105X49526

Sørensen, H. J., Mortensen, E. L., Reinisch, J. M., & Mednick, S. A. (2009). Association between prenatal exposure to bacterial infection and risk of schizophrenia. Schizophrenia bulletin, 35(3), 631–637. https://doi.org/10.1093/schbul/sbn121

Suvisaari, J., Haukka, J., Tanskanen, A., Hovi, T., & Lönnqvist, J. (1999). Association between prenatal exposure to poliovirus infection and adult schizophrenia. The American journal of psychiatry, 156(7), 1100–1102. https://doi.org/10.1176/ajp.156.7.1100

Tita, A. T., & Andrews, W. W. (2010). Diagnosis and management of clinical chorioamnionitis. Clinics in perinatology, 37(2), 339–354. https://doi.org/10.1016/j.clp.2010.02.003

Toth, C., Harder, S., & Yager, J. (2003). Neonatal herpes encephalitis: a case series and review of clinical presentation. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 30(1), 36–40. https://doi.org/10.1017/s0317167100002419

Ueda, K., Tokugawa, K., Nishida, Y., & Kimura, M. (1986). Incidence of congenital rubella syndrome in Japan (1965-1985). A nationwide survey of the number of deaf children with history of maternal rubella attending special schools for the deaf in Japan. American journal of epidemiology, 124(5), 807–815. https://doi.org/10.1093/oxfordjournals.aje.a114457

Varatharaj, A., Nicoll, J. A., Pelosi, E., & Pinto, A. A. (2017). Corticosteroid-responsive focal granulomatous herpes simplex type-1 encephalitis in adults. Practical neurology, 17(2), 140–144. https://doi.org/10.1136/practneurol-2016-001474

Vivanti, A. J., Vauloup-fellous, C., Prevot, S., Zupan, V., Suffee, C., Cao, J. Do, & Luca, D. De. (n.d.). infection. Nature Communications, (2020), 1–7. https://doi.org/10.1038/s41467-020-17436-6

Von Kohorn, I., Stein, S. R., Shikani, B. T., Ramos-Benitez, M. J., Vannella, K. M., Hewitt, S. M., Kleiner, D. E., Alejo, J. C., Burbelo, P., Cohen, J. I., Wiedermann, B. L., & Chertow, D. S. (2020). In Utero Severe Acute Respiratory Syndrome Coronavirus 2 Infection. Journal of the Pediatric Infectious Diseases Society, 9(6), 769–771. https://doi.org/10.1093/jpids/piaa127

Walter, S., Atkinson, C., Sharland, M., Rice, P., Raglan, E., Emery, V. C., & Griffiths, P. D. (2008). Congenital cytomegalovirus: association between dried blood spot viral load and hearing loss. Archives of disease in childhood. Fetal and neonatal edition, 93(4), F280–F285. https://doi.org/10.1136/adc.2007.119230

Wang, T., Zhou, J., Gan, X., Wang, H., Ding, X., Chen, L., Wang, Y., DU, J., Shen, J., & Yu, L. (2014). Toxoplasma gondii induce apoptosis of neural stem cells via endoplasmic reticulum stress pathway. Parasitology, 141(7), 988–995. https://doi.org/10.1017/S0031182014000183

Webster W. S. (1998). Teratogen update: congenital rubella. Teratology, 58(1), 13–23. https://doi.org/10.1002/(SICI)1096-9926(199807)58:1<13::AID-TERA5>3.0.CO;2-2

Yamamoto, S., Nagamori, T., & Komatsu, S. (2020). Case Report A case of congenital herpes simplex virus infection diagnosed at 8 months of age. Brain and Development, 42(4), 369–372. https://doi.org/10.1016/j.braindev.2020.01.003

Yamashita, Y., Matsuishi, T., Murakami, Y., Shoji, H., Hashimoto, T., Utsunomiya, H., & Araki, H. (1991). Neuroimaging findings (ultrasonography, CT, MRI) in 3 infants with congenital rubella syndrome. Pediatric radiology, 21(8), 547–549. https://doi.org/10.1007/BF02012592

Yap, M., Debenham, L., Kew, T., Chatterjee, S. R., Allotey, J., Stallings, E., Coomar, D., Lee, S. I., Qiu, X., Yuan, M., Clavé Llavall, A., Dixit, A., Zhou, D., Balaji, R., van Wely, M., Kostova, E., van Leeuwen, E., Mofenson, L., Kunst, H., Khalil, A., … PregCOV-19 Consortium (2020). Clinical manifestations, prevalence, risk factors, outcomes, transmission, diagnosis and treatment of COVID-19 in pregnancy and postpartum: a living systematic review protocol. BMJ open, 10(12), e041868. https://doi.org/10.1136/bmjopen-2020-041868

Yarovinsky, F., Zhang, D., Andersen, J. F., Bannenberg, G. L., Serhan, C. N., Hayden, M. S., Hieny, S., Sutterwala, F. S., Flavell, R. A., Ghosh, S., & Sher, A. (2005). TLR11 activation of dendritic cells by a protozoan profilin-like protein. Science (New York, N.Y.), 308(5728), 1626–1629. https://doi.org/10.1126/science.1109893

Yazigi, A., De Pecoulas, A. E., Vauloup-Fellous, C., Grangeot-Keros, L., Ayoubi, J. M., & Picone, O. (2017). Fetal and neonatal abnormalities due to congenital rubella syndrome: a review of literature. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 30(3), 274–278. https://doi.org/10.3109/14767058.2016.1169526

Zammit, S., Odd, D., Horwood, J., Thompson, A., Thomas, K., Menezes, P., Gunnell, D., Hollis, C., Wolke, D., Lewis, G., & Harrison, G. (2009). Investigating whether adverse prenatal and perinatal events are associated with non-clinical psychotic symptoms at age 12 years in the ALSPAC birth cohort. Psychological medicine, 39(9), 1457–1467. https://doi.org/10.1017/S0033291708005126

Zhang, X., Su, R., Cheng, Z., Zhu, W., Li, Y., Wang, Y., Du, J., Cai, Y., Luo, Q., Shen, J., & Yu, L. (2017). A mechanistic study of Toxoplasma gondii ROP18 inhibiting differentiation of C17.2 neural stem cells. Parasites & vectors, 10(1), 585. https://doi.org/10.1186/s13071-017-2529-2

Referanslar

Adamo, P., Asís, L., Silveyra, P., Cuffini, C., Pedranti, M. & Zapata, M. (2004). Rubella virus does not ınduce apoptosis in primary human embryo fibroblast cultures: A possible way of viral persistence in congenital Infection. Viral Immunology, 17(1), 87–100.

Al-awaidy, S., Griffiths, U.K., Mohammed, H., Bawikar, S., Al-aisiri, M. S., Khandekar, R. & Robertson, S.E. (2006). Costs of congenital rubella syndrome (CRS) in Oman : Evidence based on long-term follow-up of 43 children. Vaccine, 24, 6437–6445.

Al-haddad, B.J.S., Oler, E., Armistead, B., Elsayed, N.A., Weinberger, D.R., Bernier, R. & … Waldorf, K.M.A. (2020). The fetal origins of mental illness. Am J Obstet Gynecol, 221(6), 549–562.

Allotey, J., Chatterjee, S., Kew, T., Gaetano, A., Stallings, E., Fernández-garcía, S. & … Thangaratinam, S. (2022). SARS-CoV-2 positivity in offspring and timing of mother-to-child transmission : living systematic review and meta-analysis. BMJ, 376, 1–11.

Andersen R. D. (1987). Herpes simplex virus infection of the neonatal respiratory tract. American journal of diseases of children (1960), 141(3), 274–276. https://doi.org/10.1001/archpedi.1987.04460030052023

Angelone, D.F., Wessels, M.R., Coughlin, M., Suter, E.E., Valentini, P., Kalish, L.A. &… Boston, H. (2006). Innate ımmunity of the human newborn is polarized toward a high ratio of IL-6/TNF- alpha production in vitro and in vivo. Pediatr Res, 60(2), 205–209. https://doi.org/10.1203/01.pdr.0000228319.10481.ea

Ashary, N., Bhide, A., Chakraborty, P. & Colaco, S. (2020). Single- Cell RNA -seq identifies cell subsets in human placenta that highly expresses factors driving pathogenesis of SARS-CoV-2. Front Cell Dev Biol, 8, 1–16. https://doi.org/10.3389/fcell.2020.00783

Atladóttir, H. O., Thorsen, P., Østergaard, L., Schendel, D. E., Lemcke, S., Abdallah, M., & Parner, E. T. (2010). Maternal infection requiring hospitalization during pregnancy and autism spectrum disorders. Journal of autism and developmental disorders, 40(12), 1423–1430. https://doi.org/10.1007/s10803-010-1006-y

Ayed, M., Embaireeg, A., Kartam, M., More, K., Alqallaf, M., Alnafisi, A., Fouzan, W.A. & Hessa Alkandari. (2022). Neurodevelopmental outcomes of infants born to mothers with SARS‑CoV‑2 infections during pregnancy: A national prospective study in Kuwait. BMC Pediatrics, 22, 1–11. https://doi.org/10.1186/s12887-022-03359-2

Bale, J.F. (2009). Fetal infections and brain development. Clin Perinatol, 36, 639–653. https://doi.org/10.1016/j.clp.2009.06.005

Balistreri, W. F. & Journal, T. (2008). When Should You Initiate Acyclovir Therapy in a Neonate? J Pediatr, 153(2), 155-6. doi: 10.1016/j.jpeds.2008.04.027.

Banatvala, J.E. & Brown, D.W.G. (2004). Rubella. Lancet, 363(9415), 1127-1137. doi: 10.1016/S0140-6736(04)15897-2.

Barry, H. & Barry, H. (1961). Season of Birth, Archives of General Psychiatry, 5, 292–300.

Baud, O., Fontaine, R. H., Olivier, P., Maury, L., Moussawi, F. E., Bauvin, I. & Aujard, Y. (2007). Premature rupture of membranes: pathophysiology of neurological impact. Archives de pediatrie, 14, 49-53.

Bennett, S. & Nagler, J. (2014). Images in emergency medicine. Herpes simplex virus encephalitis. Ann Emerg Med, 64(6):588, 608.

Bertero, L., Borella, F., Botta, G., Carosso, A., Cosma, S., Bovetti, M. & Benedetto, C. (2021). Placenta histopathology in SARS-CoV-2 infection: analysis of a consecutive series and comparison with control cohorts, Virchows Arch, 479(4):715-728. doi: 10.1007/s00428-021-03097-3.

Boksa, P. (2010). Brain , Behavior , and Immunity Effects of prenatal infection on brain development and behavior: A review of findings from animal models. Brain Behav Immun, 24(6):881-97. doi: 10.1016/j.bbi.2010.03.005.

Bonthius, D. J., Nichols, B., Harb, H. & Mahoney, J. (2007). Lymphocytic Choriomeningitis Virus Infection of the Developing Brain: Critical Role of Host Age. Ann Neurol, 62(4):356-374. doi:10.1002/ana.21193.

Boudaouara, Y., Aoun, K., Maatoug, R., Souissi, O. & Abdallah, R. Ben. (2018). Congenital Toxoplasmosis in Tunisia: Prenatal and Neonatal Diagnosis and Postnatal Follow-up of 35 Cases. Am J Trop Med Hyg, 98(6), 1722–1726. https://doi.org/10.4269/ajtmh.17-0580

Brown, A.S., Schaefer, C.A., Wyatt, R.J., Qoetz, R., Begg, M.D., Qorman, J.M. & Susser, E. S. (1996). Maternal Exposure to Respiratory Infections and Adult Schizophrenia Spectrum Disorders: A Prospective Birth Cohort Study. Schizophr Bull, 26(2), 287–296

Brown, Z. A., Benedetti, J., Ashley, R., Burchett, S., Selke, S., Berry, S., Vontver, L. A., & Corey, L. (1991). Neonatal herpes simplex virus infection in relation to asymptomatic maternal infection at the time of labor. The New England journal of medicine, 324(18), 1247–1252. https://doi.org/10.1056/NEJM199105023241804

Burd, I., Balakrishnan, B. & Kannan, S. (2012). Models of fetal brain injury, intrauterine inflammation , and Preterm Birth. Am J Reprod Immunol, 67(4), 287–295. https://doi.org/10.1111/j.1600-0897.2012.01110.x

Callaghan, E.O., Sham, P.C., Takei, N., Murray, G., Glover, G., Hare, E.H. & Murray, R.M. (1994). The Relationship of Schizophrenic Births to 16 Infectious Diseases. Br J Psychiatry, 165(3), 353–356.

Carson, M.J., Doose, J.M., Melchior, B., Schmid, C.D. & Ploix, C.C. (2009). CNS immune privilege : hiding in plain sight. Immunol Rev, 213, 48–65. https://doi.org/10.1111/j.1600-065X.2006.00441.x.CNS

Caviness, A. C., Demmler, G. J., Almendarez, Y., & Selwyn, B. J. (2008). The prevalence of neonatal herpes simplex virus infection compared with serious bacterial illness in hospitalized neonates. The Journal of pediatrics, 153(2), 164–169. https://doi.org/10.1016/j.jpeds.2008.02.031

Cheeran, M.C., Lokensgard, J.R. & Schleiss, M.R. (2009). Neuropathogenesis of Congenital Cytomegalovirus Infection: Disease Mechanisms and Prospects for Intervention. Clin Microbiol Rev, 22(1), 99–126. https://doi.org/10.1128/CMR.00023-08

Cluver, C., Meyer, R., Odendaal, H. & Geerts, L. (2013). Congenital rubella with agenesis of the inferior cerebellar vermis and total anomalous pulmonary venous drainage. Ultrasound Obstet Gynecol, 42(2), 235–237. https://doi.org/10.1002/uog.12399

Cooper, L.Z. (1985). The History and Medical Consequences of Rubella. Rev Infect Dis, 7, 2-10. doi: 10.1093/clinids/7.supplement_1.s2.

Corey, L., Whitley, R. J., Stone, E. F., & Mohan, K. (1988). Difference between herpes simplex virus type 1 and type 2 neonatal encephalitis in neurological outcome. Lancet (London, England), 1(8575-6), 1–4. https://doi.org/10.1016/s0140-6736(88)90997-x

Cradock-watson, J.E. & Pollock, T.M. (1982). Consequences of confirmed maternal rubella at successive stages of pregnancy. Lancet, 2(8302), 781-784. doi: 10.1016/s0140-6736(82)92677-0.

Desmond, M.M., Wilson, G.S., Vorderman, A.L., Murphy, M.A., Fisher, E.S. & Kroulik, E.M. (1967). The health and educational status of adolescents with congenital rubella syndrome. Dev Med Child Neurol, 27(6),721-729. doi: 10.1111/j.1469-8749.1985.tb03795.x.

Desmonts, G. & Couvreur, J. (1974). Congenital toxoplasmosis. A prospective study of 378 pregnancies. N Engl J Med, 290(20), 1110-1116. doi: 10.1056/NEJM197405162902003

Dudgeon J. A. (1975). Congenital rubella. The Journal of pediatrics, 87(6 Pt 2), 1078–1086. https://doi.org/10.1016/s0022-3476(75)80119-3

Duncan, R., Muller, J., Lee, N., Esmaili, A. & Nakhasi, H.L. (1999). Rubella Virus-Induced Apoptosis Varies among Cell Lines and Is Modulated by Bcl-X L and Caspase Inhibitors. Virology, 255(1), 117–128.

Durukan, D., Fairley, C.K., Bradshaw, C.S., Read, T.R.H., Druce, J., Catton, M. & Chow, E. P.F. (2018). Increasing proportion of herpes simplex virus type 1 among women and men diagnosed with first-episode anogenital herpes: A retrospective observational study over 14 years in Melbourne , Australia, Sex Transm Infect, 95(4), 307-313. https://doi.org/10.1136/sextrans-2018-053830

Edlow, A.G., Castro, V.M., Shook, L.L., Kaimal, A.J. & Perlis, R.H. (2022). Neurodevelopmental Outcomes at 1 Year in Infants of Mothers Who Tested Positive for SARS-CoV-2 During Pregnancy, JAMA Netw Open, 5(6), 1–10. https://doi.org/10.1001/jamanetworkopen.2022.15787

Engert, V., Siauw, C., Stock, A., Rehn, M., Wöckel, A., Härtel, C. & Wirbelauer, J. (2021). Severe Brain Damage in a Moderate Preterm Infant as Complication of Post-COVID-19 Response during Pregnancy. Neonatology, 118(4), 505-508. https://doi.org/10.1159/000516846

Esiri M. M. (1982). Herpes simplex encephalitis. An immunohistological study of the distribution of viral antigen within the brain. Journal of the neurological sciences, 54(2), 209–226. https://doi.org/10.1016/0022-510x(82)90183-6

Estato, V., Stipursky, J., Gomes, F., Mergener, T.C., Frazão-teixeira, E., Allodi, S. & Adesse, D. (2018). The Neurotropic Parasite Toxoplasma gondii Induces Sustained Neuroin fl ammation with Microvascular Dysfunction in Infected Mice. The American Journal of Pathology, 188(11), 2674–2687. https://doi.org/10.1016/j.ajpath.2018.07.007

Fernandes, A. F., Lange, M. C., Novak, F. T., Zavala, J. A., Zamproni, L. N., Germiniani, F. M., Piovesan, E. J., & Teive, H. A. (2010). Extra-temporal involvement in herpes simplex encephalitis. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 17(9), 1221–1223 https://doi.org/10.1016/j.jocn.2010.02.007

French, R. R., & York, D. A. (1984). The regulation of adenylate cyclase in adipocyte plasma membrane from genetically obese (ob/ob) mice. Diabetologia, 26(6), 466–472. https://doi.org/10.1007/BF00262223

Gabrielli, L., Bonasoni, M. P., Santini, D., Piccirilli, G., Chiereghin, A., Petrisli, E. & Piccioli, M. (2012). Congenital cytomegalovirus infection: patterns of fetal brain damage. Clin Microbiol Infect, 18(10), 419-427.

Gan, X., Zhang, X., Cheng, Z., Chen, L., Ding, X., Du, J. & Yu, L. (2016). Toxoplasma gondii inhibits differentiation of C17.2 neural stem cells through Wnt/β-catenin signaling pathway. Biochem Biophys Res Commun, 473(1), 187-193. https://doi.org/10.1016/j.bbrc.2016.03.076

Germano, C., Messina, A., Tavella, E., Vitale, R., Avellis, V., Barboni, M., Attini, R., Revelli, A., Zola, P., Manzoni, P., & Masturzo, B. (2022). Fetal Brain Damage during Maternal COVID-19: Emerging Hypothesis, Mechanism, and Possible Mitigation through Maternal-Targeted Nutritional Supplementation. Nutrients, 14(16), 3303. https://doi.org/10.3390/nu14163303

Gordon-lipkin, E., Hoon, A. & Pardo, C.A. (2022). Prenatal cytomegalovirus, rubella, and Zika virus infections associated with developmental disabilities: past, present, and future. Dev Med Child Neurol, 63(2), 135–143. https://doi.org/10.1111/dmcn.14682.Prenatal

Gordon-Lipkin, E., & Peacock, G. (2019). The Spectrum of Developmental Disability with Zika Exposure: What Is Known, What Is Unknown, and Implications for Clinicians. Journal of developmental and behavioral pediatrics: JDBP, 40(5), 387–395. https://doi.org/10.1097/DBP.0000000000000665

Gordon, B. & Neilson, M. (1975). Mental disorder and season of birth--a southern hemisphere study. Br J Psychiatry, 129, 355–361.

Gregg, N. M. & Banatvala, R. J. E. (2001). Congenital cataract following German measles in the mother. 1941. Aust N Z J Ophthalmol, 19(4), 267-76.

Hecht, J. L., Quade, B., Deshpande, V., David, M. M., Desai, N., Dygulska, B., Bates, S.V. & Roberts, D.J. (2020). SARS-CoV-2 can infect the placenta and is not associated with specific placental histopathology: a series of 19 placentas from COVID-19-positive mothers. Mod Pathol, 33(11), 2092-2103.

Hermes, G., Ajioka, J. W., Kelly, K. A., Mui, E., Roberts, F., Kasza, K., Mayr, T., Kirisits, M. J., Wollmann, R., Ferguson, D. J., Roberts, C. W., Hwang, J. H., Trendler, T., Kennan, R. P., Suzuki, Y., Reardon, C., Hickey, W. F., Chen, L., & McLeod, R. (2008). Neurological and behavioral abnormalities, ventricular dilatation, altered cellular functions, inflammation, and neuronal injury in brains of mice due to common, persistent, parasitic infection. Journal of neuroinflammation, 5, 48. https://doi.org/10.1186/1742-2094-5-48

Huang, P., Zhou, F., Guo, Y., Yuan, S., Lin, S., Lu, J., Tu, S., Lu, M., Shen, S., Guedeney, A., Xia, H., & Qiu, X. (2021). Association Between the COVID-19 Pandemic and Infant Neurodevelopment: A Comparison Before and During COVID-19. Frontiers in pediatrics, 9, 662165. https://doi.org/10.3389/fped.2021.662165

Hudson, S. J., Dix, R. D., & Streilein, J. W. (1991). Induction of encephalitis in SJL mice by intranasal infection with herpes simplex virus type 1: a possible model of herpes simplex encephalitis in humans. The Journal of infectious diseases, 163(4), 720–727. https://doi.org/10.1093/infdis/163.4.720

Huleihel, M., Golan, H., & Hallak, M. (2004). Intrauterine infection/inflammation during pregnancy and offspring brain damages: possible mechanisms involved. Reproductive biology and endocrinology, 2, 17. https://doi.org/10.1186/1477-7827-2-17

Istas, A. S., Demmler, G. J., Dobbins, J. G., & Stewart, J. A. (1995). Surveillance for congenital cytomegalovirus disease: a report from the National Congenital Cytomegalovirus Disease Registry. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 20(3), 665–670. https://doi.org/10.1093/clinids/20.3.665

Jamieson, D. J., Ellis, J. E., Jernigan, D. B., & Treadwell, T. A. (2006). Emerging infectious disease outbreaks: old lessons and new challenges for obstetrician-gynecologists. American journal of obstetrics and gynecology, 194(6), 1546–1555. https://doi.org/10.1016/j.ajog.2005.06.062

Long S. S. (2008). In defense of empiric acyclovir therapy in certain neonates. The Journal of pediatrics, 153(2), 157–158. https://doi.org/10.1016/j.jpeds.2008.04.071

Kimberlin D.W. (2004). Neonatal herpes simplex infection. Clinical microbiology reviews, 17(1), 1–13. https://doi.org/10.1128/CMR.17.1.1-13.2004

Koch, L. H., Fisher, R. G., Chen, C., Foster, M. M., Bass, W. T., & Williams, J. V. (2009). Congenital herpes simplex virus infection: two unique cutaneous presentations associated with probable intrauterine transmission. Journal of the American Academy of Dermatology, 60(2), 312–315. https://doi.org/10.1016/j.jaad.2008.08.038

Lazarte-Rantes, C., Rodríguez-Anccasi, R., Rivas-Campos, C., & Silva, E. (2021). Congenital Toxoplasmosis: Findings in Fetal MRI. Cureus, 13(8), e16894. https://doi.org/10.7759/cureus.16894

Leas, B. F., & Umscheid, C. A. (2015). Neonatal Herpes Simplex Virus Type 1 Infection and Jewish Ritual Circumcision With Oral Suction: A Systematic Review. Journal of the Pediatric Infectious Diseases Society, 4(2), 126–131. https://doi.org/10.1093/jpids/piu075

Lee, B. K., Magnusson, C., Gardner, R. M., Blomström, Å., Newschaffer, C. J., Burstyn, I., Karlsson, H., & Dalman, C. (2015). Maternal hospitalization with infection during pregnancy and risk of autism spectrum disorders. Brain, behavior, and immunity, 44, 100–105. https://doi.org/10.1016/j.bbi.2014.09.001

Lee, J. Y., & Bowden, D. S. (2000). Rubella virus replication and links to teratogenicity. Clinical microbiology reviews, 13(4), 571–587. https://doi.org/10.1128/CMR.13.4.571

Littauer, E. Q., Esser, E. S., Antao, O. Q., Vassilieva, E. V., Compans, R. W., & Skountzou, I. (2017). H1N1 influenza virus infection results in adverse pregnancy outcomes by disrupting tissue-specific hormonal regulation. PLoS pathogens, 13(11), e1006757. https://doi.org/10.1371/journal.ppat.1006757

Louie, J. K., Shaikh-Laskos, R., Preas, C., Nguyen, V. T., Peters, A., & Messenger, S. (2009). Re-emergence of another vaccine-preventable disease?-Two cases of rubella in older adults. Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology, 46(1), 98–100. https://doi.org/10.1016/j.jcv.2009.06.013

Malik, A. N., Hildebrand, G. D., Sekhri, R., & Russell-Eggitt, I. M. (2008). Bilateral macular scars following intrauterine herpes simplex virus type 2 infection. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 12(3), 305–306. https://doi.org/10.1016/j.jaapos.2008.01.002

Marquez, L., Levy, M. L., Munoz, F. M., & Palazzi, D. L. (2011). A report of three cases and review of intrauterine herpes simplex virus infection. The Pediatric infectious disease journal, 30(2), 153–157. https://doi.org/10.1097/INF.0b013e3181f55a5c

Marcos, A. C., Siqueira, M., Alvarez-Rosa, L., Cascabulho, C. M., Waghabi, M. C., Barbosa, H. S., Adesse, D., & Stipursky, J. (2020). Toxoplasma gondii infection impairs radial glia differentiation and its potential to modulate brain microvascular endothelial cell function in the cerebral cortex. Microvascular research, 131, 104024. https://doi.org/10.1016/j.mvr.2020.104024

Meaney-Delman, D., Jamieson, D. J., & Rasmussen, S. A. (2017). Addressing the effects of established and emerging infections during pregnancy. Birth defects research, 109(5), 307–310. https://doi.org/10.1002/bdr2.1018

Mednick, S. A., Machon, R. A., Huttunen, M. O., & Bonett, D. (1988). Adult schizophrenia following prenatal exposure to an influenza epidemic. Archives of general psychiatry, 45(2), 189–192. https://doi.org/10.1001/archpsyc.1988.01800260109013

Melvin, A. J., Mohan, K. M., Vora, S. B., Selke, S., Sullivan, E., & Wald, A. (2022). Neonatal Herpes Simplex Virus Infection: Epidemiology and Outcomes in the Modern Era. Journal of the Pediatric Infectious Diseases Society, 11(3), 94–101. https://doi.org/10.1093/jpids/piab105

Nguyen, T. Van, Pham, V. H., & Abe, K. (2015). EBioMedicine Pathogenesis of Congenital Rubella Virus Infection in Human Fetuses : Viral Infection in the Ciliary Body Could Play an Important Role in Cataractogenesis. EBIOM, 2(1), 59–63. https://doi.org/10.1016/j.ebiom.2014.10.021

Orenstein, W. A., Bart, K. J., Hinman, A. R., Preblud, S. R., Greaves, W. L., Doster, S. W., Stetler, H. C., & Sirotkin, B. (1984). The opportunity and obligation to eliminate rubella from the United States. JAMA, 251(15), 1988–1994.

Palmer, C., Towfighi, J., Roberts, R. L., & Heitjan, D. F. (1993). Allopurinol administered after inducing hypoxia-ischemia reduces brain injury in 7-day-old rats. Pediatric research, 33(4 Pt 1), 405–411. https://doi.org/10.1203/00006450-199304000-00018

Pappas, G., Roussos, N., & Falagas, M. E. (2009). Toxoplasmosis snapshots : Global status of Toxoplasma gondii seroprevalence and implications for pregnancy and congenital toxoplasmosis. International Journal for Parasitology, 39(12), 1385–1394. https://doi.org/10.1016/j.ijpara.2009.04.003

Parisot, S., Droulle, P., Feldmann, M., Pinaud, P., & Marchal, C. (1991). Unusual encephaloclastic lesions with paraventricular calcification in congenital rubella. Pediatric radiology, 21(3), 229–230. https://doi.org/10.1007/BF02011057

Park, C., Moon, K. C., Park, J. S., Jun, J. K., & Yoon, B. H. (2009). The Frequency and Clinical Significance of Intra-Uterine Infection and Inflammation in Patients with Placenta Previa and Preterm Labor and Intact Membranes. Placenta, 30(7), 613–618. https://doi.org/10.1016/j.placenta.2009.04.005

Petito, C. K., Torres-Muñoz, J. E., Zielger, F., & McCarthy, M. (2006). Brain CD8+ and cytotoxic T lymphocytes are associated with, and may be specific for, human immunodeficiency virus type 1 encephalitis in patients with acquired immunodeficiency syndrome. Journal of neurovirology, 12(4), 272–283. https://doi.org/10.1080/13550280600879204

Plotkin S. A. (2006). The history of rubella and rubella vaccination leading to elimination. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 43 Suppl 3, S164–S168. https://doi.org/10.1086/505950

Prabhu, M., & Riley, L. E. (2023). Coronavirus Disease 2019 (COVID-19) Vaccination in Pregnancy. Obstetrics and gynecology, 141(3), 473–482. https://doi.org/10.1097/AOG.0000000000005100

Ramiro-Cortijo, D., de la Calle, M., Böger, R., Hannemann, J., Lüneburg, N., López-Giménez, M. R., Rodríguez-Rodríguez, P., Martín-Cabrejas, M. Á., Benítez, V., de Pablo, Á. L. L., González, M. D. C., & Arribas, S. M. (2020). Male fetal sex is associated with low maternal plasma anti-inflammatory cytokine profile in the first trimester of healthy pregnancies. Cytokine, 136, 155290. https://doi.org/10.1016/j.cyto.2020.155290

Raony, Í., de Figueiredo, C. S., Pandolfo, P., Giestal-de-Araujo, E., Oliveira-Silva Bomfim, P., & Savino, W. (2020). Psycho-Neuroendocrine-Immune Interactions in COVID-19: Potential Impacts on Mental Health. Frontiers in immunology, 11, 1170. https://doi.org/10.3389/fimmu.2020.01170

Reef, S. E., Redd, S. B., Abernathy, E., Zimmerman, L., & Icenogle, J. P. (2006). The epidemiological profile of rubella and congenital rubella syndrome in the United States, 1998-2004: the evidence for absence of endemic transmission. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 43 Suppl 3, S126–S132. https://doi.org/10.1086/505944

Rorke, L. B., & Spiro, A. J. (1967). Cerebral lesions in congenital rubella syndrome. The Journal of pediatrics, 70(2), 243–255. https://doi.org/10.1016/s0022-3476(67)80419-0

Saito, K., Packianathan, S., & Longo, L. D. (1997). Free radical-induced elevation of ornithine decarboxylase activity in developing rat brain slices. Brain research, 763(2), 232–238. https://doi.org/10.1016/s0006-8993(97)00414-9

Saxon, S. A., Knight, W., Reynolds, D. W., Stagno, S., & Alford, C. A. (1973). Intellectual deficits in children born with subclinical congenital toxoplasmosis: a preliminary report. The Journal of pediatrics, 82(5), 792–797. https://doi.org/10.1016/s0022-3476(73)80068-x

Seckl, J. R., & Holmes, M. C. (2007). Mechanisms of disease: glucocorticoids, their placental metabolism and fetal 'programming' of adult pathophysiology. Nature clinical practice. Endocrinology & metabolism, 3(6), 479–488. https://doi.org/10.1038/ncpendmet0515

Shanes, E. D., Mithal, L. B., Otero, S., Azad, H. A., Miller, E. S., & Goldstein, J. A. (2020). Placental Pathology in COVID-19. American journal of clinical pathology, 154(1), 23–32. https://doi.org/10.1093/ajcp/aqaa089

Sheinbergas, M.M. (1976). Hydrocephalus due to Prenatal Infection with the Lymphocytic Choriomeningitis Virus. Infection, 4(4), 185–191

Shook, L. L., & Edlow, A. G. (2023). Safety and Efficacy of Coronavirus Disease 2019 (COVID-19) mRNA Vaccines During Lactation. Obstetrics and gynecology, 141(3), 483–491. https://doi.org/10.1097/AOG.0000000000005093

Simard, A. R., & Rivest, S. (2005). Do pathogen exposure and innate immunity cause brain diseases?. Neurological research, 27(7), 717–725. https://doi.org/10.1179/016164105X49526

Sørensen, H. J., Mortensen, E. L., Reinisch, J. M., & Mednick, S. A. (2009). Association between prenatal exposure to bacterial infection and risk of schizophrenia. Schizophrenia bulletin, 35(3), 631–637. https://doi.org/10.1093/schbul/sbn121

Suvisaari, J., Haukka, J., Tanskanen, A., Hovi, T., & Lönnqvist, J. (1999). Association between prenatal exposure to poliovirus infection and adult schizophrenia. The American journal of psychiatry, 156(7), 1100–1102. https://doi.org/10.1176/ajp.156.7.1100

Tita, A. T., & Andrews, W. W. (2010). Diagnosis and management of clinical chorioamnionitis. Clinics in perinatology, 37(2), 339–354. https://doi.org/10.1016/j.clp.2010.02.003

Toth, C., Harder, S., & Yager, J. (2003). Neonatal herpes encephalitis: a case series and review of clinical presentation. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 30(1), 36–40. https://doi.org/10.1017/s0317167100002419

Ueda, K., Tokugawa, K., Nishida, Y., & Kimura, M. (1986). Incidence of congenital rubella syndrome in Japan (1965-1985). A nationwide survey of the number of deaf children with history of maternal rubella attending special schools for the deaf in Japan. American journal of epidemiology, 124(5), 807–815. https://doi.org/10.1093/oxfordjournals.aje.a114457

Varatharaj, A., Nicoll, J. A., Pelosi, E., & Pinto, A. A. (2017). Corticosteroid-responsive focal granulomatous herpes simplex type-1 encephalitis in adults. Practical neurology, 17(2), 140–144. https://doi.org/10.1136/practneurol-2016-001474

Vivanti, A. J., Vauloup-fellous, C., Prevot, S., Zupan, V., Suffee, C., Cao, J. Do, & Luca, D. De. (n.d.). infection. Nature Communications, (2020), 1–7. https://doi.org/10.1038/s41467-020-17436-6

Von Kohorn, I., Stein, S. R., Shikani, B. T., Ramos-Benitez, M. J., Vannella, K. M., Hewitt, S. M., Kleiner, D. E., Alejo, J. C., Burbelo, P., Cohen, J. I., Wiedermann, B. L., & Chertow, D. S. (2020). In Utero Severe Acute Respiratory Syndrome Coronavirus 2 Infection. Journal of the Pediatric Infectious Diseases Society, 9(6), 769–771. https://doi.org/10.1093/jpids/piaa127

Walter, S., Atkinson, C., Sharland, M., Rice, P., Raglan, E., Emery, V. C., & Griffiths, P. D. (2008). Congenital cytomegalovirus: association between dried blood spot viral load and hearing loss. Archives of disease in childhood. Fetal and neonatal edition, 93(4), F280–F285. https://doi.org/10.1136/adc.2007.119230

Wang, T., Zhou, J., Gan, X., Wang, H., Ding, X., Chen, L., Wang, Y., DU, J., Shen, J., & Yu, L. (2014). Toxoplasma gondii induce apoptosis of neural stem cells via endoplasmic reticulum stress pathway. Parasitology, 141(7), 988–995. https://doi.org/10.1017/S0031182014000183

Webster W. S. (1998). Teratogen update: congenital rubella. Teratology, 58(1), 13–23. https://doi.org/10.1002/(SICI)1096-9926(199807)58:1<13::AID-TERA5>3.0.CO;2-2

Yamamoto, S., Nagamori, T., & Komatsu, S. (2020). Case Report A case of congenital herpes simplex virus infection diagnosed at 8 months of age. Brain and Development, 42(4), 369–372. https://doi.org/10.1016/j.braindev.2020.01.003

Yamashita, Y., Matsuishi, T., Murakami, Y., Shoji, H., Hashimoto, T., Utsunomiya, H., & Araki, H. (1991). Neuroimaging findings (ultrasonography, CT, MRI) in 3 infants with congenital rubella syndrome. Pediatric radiology, 21(8), 547–549. https://doi.org/10.1007/BF02012592

Yap, M., Debenham, L., Kew, T., Chatterjee, S. R., Allotey, J., Stallings, E., Coomar, D., Lee, S. I., Qiu, X., Yuan, M., Clavé Llavall, A., Dixit, A., Zhou, D., Balaji, R., van Wely, M., Kostova, E., van Leeuwen, E., Mofenson, L., Kunst, H., Khalil, A., … PregCOV-19 Consortium (2020). Clinical manifestations, prevalence, risk factors, outcomes, transmission, diagnosis and treatment of COVID-19 in pregnancy and postpartum: a living systematic review protocol. BMJ open, 10(12), e041868. https://doi.org/10.1136/bmjopen-2020-041868

Yarovinsky, F., Zhang, D., Andersen, J. F., Bannenberg, G. L., Serhan, C. N., Hayden, M. S., Hieny, S., Sutterwala, F. S., Flavell, R. A., Ghosh, S., & Sher, A. (2005). TLR11 activation of dendritic cells by a protozoan profilin-like protein. Science (New York, N.Y.), 308(5728), 1626–1629. https://doi.org/10.1126/science.1109893

Yazigi, A., De Pecoulas, A. E., Vauloup-Fellous, C., Grangeot-Keros, L., Ayoubi, J. M., & Picone, O. (2017). Fetal and neonatal abnormalities due to congenital rubella syndrome: a review of literature. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 30(3), 274–278. https://doi.org/10.3109/14767058.2016.1169526

Zammit, S., Odd, D., Horwood, J., Thompson, A., Thomas, K., Menezes, P., Gunnell, D., Hollis, C., Wolke, D., Lewis, G., & Harrison, G. (2009). Investigating whether adverse prenatal and perinatal events are associated with non-clinical psychotic symptoms at age 12 years in the ALSPAC birth cohort. Psychological medicine, 39(9), 1457–1467. https://doi.org/10.1017/S0033291708005126

Zhang, X., Su, R., Cheng, Z., Zhu, W., Li, Y., Wang, Y., Du, J., Cai, Y., Luo, Q., Shen, J., & Yu, L. (2017). A mechanistic study of Toxoplasma gondii ROP18 inhibiting differentiation of C17.2 neural stem cells. Parasites & vectors, 10(1), 585. https://doi.org/10.1186/s13071-017-2529-2

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