Özel Gereksinimi Olan Çocuklarda Beyin Gelişimi

Al-Mahrezi, A., Al-Futaisi, A., & Al-Mamari, W. (2016). Learning Disabilities: Opportunities and challenges in Oman. Sultan Qaboos Univ Med J, 16(2), e129-131. https://doi.org/10.18295/squmj.2016.16.02.001

Arya, R., Kabra, M., & Gulati, S. (2011). Epilepsy in children with Down syndrome. Epileptic Disord, 13(1), 1-7. https://doi.org/10.1684/epd.2011.0415

Ashwal, S., Russman, B. S., Blasco, P. A., Miller, G., Sandler, A., Shevell, M., & Stevenson, R. (2004). Practice parameter: diagnostic assessment of the child with cerebral palsy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology, 62(6), 851-863. https://doi.org/10.1212/01.wnl.0000117981.35364.1b

Baburamani, A. A., Patkee, P. A., Arichi, T., & Rutherford, M. A. (2019). New approaches to studying early brain development in Down syndrome. Dev Med Child Neurol, 61(8), 867-879. https://doi.org/10.1111/dmcn.14260

Bai, D., Yip, B. H. K., Windham, G. C., Sourander, A., Francis, R., Yoffe, R., Glasson, E., Mahjani, B., Suominen, A., Leonard, H., Gissler, M., Buxbaum, J. D., Wong, K., Schendel, D., Kodesh, A., Breshnahan, M., Levine, S. Z., Parner, E. T., Hansen, S. N., . . . Sandin, S. (2019). Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort. JAMA Psychiatry, 76(10), 1035-1043. https://doi.org/10.1001/jamapsychiatry.2019.1411

Bauman, M. L., & Kemper, T. L. (2003). The neuropathology of the autism spectrum disorders: what have we learned? Novartis Found Symp, 251, 112-122; discussion 122-118, 281-197.

Bax, M., Goldstein, M., Rosenbaum, P., Leviton, A., Paneth, N., Dan, B., Jacobsson, B., & Damiano, D. (2005). Proposed definition and classification of cerebral palsy, April 2005. Dev Med Child Neurol, 47(8), 571-576. https://doi.org/10.1017/s001216220500112x

Bosanquet, M., Copeland, L., Ware, R., & Boyd, R. (2013). A systematic review of tests to predict cerebral palsy in young children. Dev Med Child Neurol, 55(5), 418-426. https://doi.org/10.1111/dmcn.12140

de Sola, S., de la Torre, R., Sánchez-Benavides, G., Benejam, B., Cuenca-Royo, A., Del Hoyo, L., Rodríguez, J., Catuara-Solarz, S., Sanchez-Gutierrez, J., Dueñas-Espin, I., Hernandez, G., Peña-Casanova, J., Langohr, K., Videla, S., Blehaut, H., Farre, M., & Dierssen, M. (2015). A new cognitive evaluation battery for Down syndrome and its relevance for clinical trials. Front Psychol, 6, 708. https://doi.org/10.3389/fpsyg.2015.00708

DiGuiseppi, C., Hepburn, S., Davis, J. M., Fidler, D. J., Hartway, S., Lee, N. R., Miller, L., Ruttenber, M., & Robinson, C. (2010). Screening for autism spectrum disorders in children with Down syndrome: population prevalence and screening test characteristics. J Dev Behav Pediatr, 31(3), 181-191. https://doi.org/10.1097/DBP.0b013e3181d5aa6d

El Hajj, N., Dittrich, M., Böck, J., Kraus, T. F., Nanda, I., Müller, T., Seidmann, L., Tralau, T., Galetzka, D., & Schneider, E. J. E. (2016). Epigenetic dysregulation in the developing Down syndrome cortex. 11(8), 563-578.

Eliasson, A. C., & Holmefur, M. (2015). The influence of early modified constraint-induced movement therapy training on the longitudinal development of hand function in children with unilateral cerebral palsy. Dev Med Child Neurol, 57(1), 89-94. https://doi.org/10.1111/dmcn.12589

Elkamil, A. I., Andersen, G. L., Hägglund, G., Lamvik, T., Skranes, J., & Vik, T. (2011). Prevalence of hip dislocation among children with cerebral palsy in regions with and without a surveillance programme: a cross sectional study in Sweden and Norway. BMC Musculoskelet Disord, 12, 284. https://doi.org/10.1186/1471-2474-12-284

Elsabbagh, M., Divan, G., Koh, Y. J., Kim, Y. S., Kauchali, S., Marcín, C., Montiel-Nava, C., Patel, V., Paula, C. S., Wang, C., Yasamy, M. T., & Fombonne, E. (2012). Global prevalence of autism and other pervasive developmental disorders. Autism Res, 5(3), 160-179. https://doi.org/10.1002/aur.239

Foster, N. E., Doyle-Thomas, K. A., Tryfon, A., Ouimet, T., Anagnostou, E., Evans, A. C., Zwaigenbaum, L., Lerch, J. P., Lewis, J. D., & Hyde, K. L. (2015). Structural Gray Matter Differences During Childhood Development in Autism Spectrum Disorder: A Multimetric Approach. Pediatr Neurol, 53(4), 350-359. https://doi.org/10.1016/j.pediatrneurol.2015.06.013

Francks, C., MacPhie, I. L., & Monaco, A. P. J. T. L. N. (2002). The genetic basis of dyslexia. 1(8), 483-490.

Frewer, V., Gilchrist, C. P., Collins, S. E., Williams, K., Seal, M. L., Leventer, R. J., & Amor, D. J. (2021). A systematic review of brain MRI findings in monogenic disorders strongly associated with autism spectrum disorder. J Child Psychol Psychiatry, 62(11), 1339-1352. https://doi.org/10.1111/jcpp.13510

Fried, P. A., Watkinson, B., Siegel, L. S. J. N., & teratology. (1997). Reading and language in 9-to 12-year olds prenatally exposed to cigarettes and marijuana. 19(3), 171-183.

Galaburda, A. M., Menard, M. T., & Rosen, G. D. J. P. o. t. N. A. o. S. (1994). Evidence for aberrant auditory anatomy in developmental dyslexia. 91(17), 8010-8013.

Galaburda, A. M., Sherman, G. F., Rosen, G. D., Aboitiz, F., Geschwind, N. J. A. o. N. O. J. o. t. A. N. A., & Society, t. C. N. (1985). Developmental dyslexia: four consecutive patients with cortical anomalies. 18(2), 222-233.

Guedj, F., Pennings, J. L., Massingham, L. J., Wick, H. C., Siegel, A. E., Tantravahi, U., & Bianchi, D. W. (2016). An Integrated Human/Murine Transcriptome and Pathway Approach To Identify Prenatal Treatments For Down Syndrome. Sci Rep, 6, 32353. https://doi.org/10.1038/srep32353

Gupta, M., Dhanasekaran, A. R., & Gardiner, K. J. (2016). Mouse models of Down syndrome: gene content and consequences. Mamm Genome, 27(11-12), 538-555. https://doi.org/10.1007/s00335-016-9661-8

Hebebrand, M., Hüffmeier, U., Trollmann, R., Hehr, U., Uebe, S., Ekici, A. B., Kraus, C., Krumbiegel, M., Reis, A., Thiel, C. T., & Popp, B. (2019). The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy. Orphanet J Rare Dis, 14(1), 38. https://doi.org/10.1186/s13023-019-1020-x

Jokiranta-Olkoniemi, E., Cheslack-Postava, K., Sucksdorff, D., Suominen, A., Gyllenberg, D., Chudal, R., Leivonen, S., Gissler, M., Brown, A. S., & Sourander, A. (2016). Risk of Psychiatric and Neurodevelopmental Disorders Among Siblings of Probands With Autism Spectrum Disorders. JAMA Psychiatry, 73(6), 622-629. https://doi.org/10.1001/jamapsychiatry.2016.0495

Kemper, T. L. (1985). Anatomical basis of learning disabilities. Brain specialization. Otolaryngol Clin North Am, 18(2), 305-314.

Lee, N. R., Adeyemi, E. I., Lin, A., Clasen, L. S., Lalonde, F. M., Condon, E., Driver, D. I., Shaw, P., Gogtay, N., & Raznahan, A. J. C. c. (2015). Dissociations in cortical morphometry in youth with Down syndrome: evidence for reduced surface area but increased thickness. 26(7), 2982-2990.

Linkersdörfer, J., Lonnemann, J., Lindberg, S., Hasselhorn, M., & Fiebach, C. J. (2012). Grey matter alterations co-localize with functional abnormalities in developmental dyslexia: an ALE meta-analysis.

Lipkin, P. H., Macias, M. M., Norwood, K. W., Brei, T. J., Davidson, L. F., Davis, B. E., Ellerbeck, K. A., Houtrow, A. J., Hyman, S. L., & Kuo, D. Z. J. P. (2020). Promoting optimal development: identifying infants and young children with developmental disorders through developmental surveillance and screening. 145(1).

Loomes, R., Hull, L., & Mandy, W. P. L. (2017). What Is the Male-to-Female Ratio in Autism Spectrum Disorder? A Systematic Review and Meta-Analysis. J Am Acad Child Adolesc Psychiatry, 56(6), 466-474. https://doi.org/10.1016/j.jaac.2017.03.013

Lord, C., Elsabbagh, M., Baird, G., & Veenstra-Vanderweele, J. (2018). Autism spectrum disorder. Lancet, 392(10146), 508-520. https://doi.org/10.1016/s0140-6736(18)31129-2

Lyle, R., Béna, F., Gagos, S., Gehrig, C., Lopez, G., Schinzel, A., Lespinasse, J., Bottani, A., Dahoun, S., & Taine, L. J. E. j. o. h. g. (2009). Genotype–phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21. 17(4), 454-466.

Määttä, T., Tervo-Määttä, T., Taanila, A., Kaski, M., & Iivanainen, M. (2006). Mental health, behaviour and intellectual abilities of people with Down syndrome. Downs Syndr Res Pract, 11(1), 37-43. https://doi.org/10.3104/reports.313

Martin, J. H., Chakrabarty, S., & Friel, K. M. (2011). Harnessing activity-dependent plasticity to repair the damaged corticospinal tract in an animal model of cerebral palsy. Dev Med Child Neurol, 53 Suppl 4(Suppl 4), 9-13. https://doi.org/10.1111/j.1469-8749.2011.04055.x

McIntyre, S., Morgan, C., Walker, K., & Novak, I. (2011). Cerebral palsy--don't delay. Dev Disabil Res Rev, 17(2), 114-129. https://doi.org/10.1002/ddrr.1106

McMichael, G., Bainbridge, M. N., Haan, E., Corbett, M., Gardner, A., Thompson, S., van Bon, B. W., van Eyk, C. L., Broadbent, J., Reynolds, C., O'Callaghan, M. E., Nguyen, L. S., Adelson, D. L., Russo, R., Jhangiani, S., Doddapaneni, H., Muzny, D. M., Gibbs, R. A., Gecz, J., & MacLennan, A. H. (2015). Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy. Mol Psychiatry, 20(2), 176-182. https://doi.org/10.1038/mp.2014.189

Morgan, C., Novak, I., Dale, R. C., Guzzetta, A., & Badawi, N. (2016). Single blind randomised controlled trial of GAME (Goals - Activity - Motor Enrichment) in infants at high risk of cerebral palsy. Res Dev Disabil, 55, 256-267. https://doi.org/10.1016/j.ridd.2016.04.005

Muhle, R. A., Reed, H. E., Stratigos, K. A., & Veenstra-VanderWeele, J. (2018). The Emerging Clinical Neuroscience of Autism Spectrum Disorder: A Review. JAMA Psychiatry, 75(5), 514-523. https://doi.org/10.1001/jamapsychiatry.2017.4685

Muthusamy, K., & Sahu, J. K. (2020). Specific Learning Disability in India: Challenges and Opportunities. Indian J Pediatr, 87(2), 91-92. https://doi.org/10.1007/s12098-019-03159-0

Novak, I., Cusick, A., & Lannin, N. (2009). Occupational therapy home programs for cerebral palsy: double-blind, randomized, controlled trial. Pediatrics, 124(4), e606-614. https://doi.org/10.1542/peds.2009-0288

Novak, I., Hines, M., Goldsmith, S., & Barclay, R. (2012). Clinical prognostic messages from a systematic review on cerebral palsy. Pediatrics, 130(5), e1285-1312. https://doi.org/10.1542/peds.2012-0924

Novak, I., Morgan, C., Adde, L., Blackman, J., Boyd, R. N., Brunstrom-Hernandez, J., Cioni, G., Damiano, D., Darrah, J., Eliasson, A. C., de Vries, L. S., Einspieler, C., Fahey, M., Fehlings, D., Ferriero, D. M., Fetters, L., Fiori, S., Forssberg, H., Gordon, A. M., . . . Badawi, N. (2017). Early, Accurate Diagnosis and Early Intervention in Cerebral Palsy: Advances in Diagnosis and Treatment. JAMA Pediatr, 171(9), 897-907. https://doi.org/10.1001/jamapediatrics.2017.1689

O'Callaghan, M. E., MacLennan, A. H., Gibson, C. S., McMichael, G. L., Haan, E. A., Broadbent, J. L., Goldwater, P. N., & Dekker, G. A. (2011). Epidemiologic associations with cerebral palsy. Obstet Gynecol, 118(3), 576-582. https://doi.org/10.1097/AOG.0b013e31822ad2dc

Oskoui, M., Coutinho, F., Dykeman, J., Jetté, N., & Pringsheim, T. (2013). An update on the prevalence of cerebral palsy: a systematic review and meta-analysis. Dev Med Child Neurol, 55(6), 509-519. https://doi.org/10.1111/dmcn.12080

Oskoui, M., Gazzellone, M. J., Thiruvahindrapuram, B., Zarrei, M., Andersen, J., Wei, J., Wang, Z., Wintle, R. F., Marshall, C. R., Cohn, R. D., Weksberg, R., Stavropoulos, D. J., Fehlings, D., Shevell, M. I., & Scherer, S. W. (2015). Clinically relevant copy number variations detected in cerebral palsy. Nat Commun, 6, 7949. https://doi.org/10.1038/ncomms8949

Pelphrey, K., Adolphs, R., & Morris, J. P. (2004). Neuroanatomical substrates of social cognition dysfunction in autism. Ment Retard Dev Disabil Res Rev, 10(4), 259-271. https://doi.org/10.1002/mrdd.20040

Pinter, J. D., Eliez, S., Schmitt, J. E., Capone, G. T., & Reiss, A. L. J. A. J. o. P. (2001). Neuroanatomy of Down’s syndrome: a high-resolution MRI study. 158(10), 1659-1665.

Rafiee, F., Rezvani Habibabadi, R., Motaghi, M., Yousem, D. M., & Yousem, I. J. (2022). Brain MRI in Autism Spectrum Disorder: Narrative Review and Recent Advances. J Magn Reson Imaging, 55(6), 1613-1624. https://doi.org/10.1002/jmri.27949

Robinson, E. B., Neale, B. M., & Hyman, S. E. (2015). Genetic research in autism spectrum disorders. Curr Opin Pediatr, 27(6), 685-691. https://doi.org/10.1097/mop.0000000000000278

Romeo, D. M., Ricci, D., Brogna, C., & Mercuri, E. (2016). Use of the Hammersmith Infant Neurological Examination in infants with cerebral palsy: a critical review of the literature. Dev Med Child Neurol, 58(3), 240-245. https://doi.org/10.1111/dmcn.12876

Rutter, M., Caspi, A., Fergusson, D., Horwood, L. J., Goodman, R., Maughan, B., Moffitt, T. E., Meltzer, H., & Carroll, J. (2004). Sex differences in developmental reading disability: new findings from 4 epidemiological studies. Jama, 291(16), 2007-2012. https://doi.org/10.1001/jama.291.16.2007

Sandin, S., Lichtenstein, P., Kuja-Halkola, R., Larsson, H., Hultman, C. M., & Reichenberg, A. (2014). The familial risk of autism. Jama, 311(17), 1770-1777. https://doi.org/10.1001/jama.2014.4144

Singh, S., Sawani, V., Deokate, M., Panchal, S., Subramanyam, A. A., Shah, H. R., & Kamath, R. M. J. I. J. C. P. (2017). Specific learning disability: A 5 year study from India. 4(3), 863-868.

Snowling, M. J., Gallagher, A., & Frith, U. (2003). Family risk of dyslexia is continuous: individual differences in the precursors of reading skill. Child Dev, 74(2), 358-373. https://doi.org/10.1111/1467-8624.7402003

Stoner, R., Chow, M. L., Boyle, M. P., Sunkin, S. M., Mouton, P. R., Roy, S., Wynshaw-Boris, A., Colamarino, S. A., Lein, E. S., & Courchesne, E. (2014). Patches of disorganization in the neocortex of children with autism. N Engl J Med, 370(13), 1209-1219. https://doi.org/10.1056/NEJMoa1307491

Styles, M., Alsharshani, D., Samara, M., Alsharshani, M., Khattab, A., Qoronfleh, M. W., & Al-Dewik, N. I. (2020). Risk factors, diagnosis, prognosis and treatment of autism. Front Biosci (Landmark Ed), 25(9), 1682-1717. https://doi.org/10.2741/4873

Yuen, R. K., Thiruvahindrapuram, B., Merico, D., Walker, S., Tammimies, K., Hoang, N., Chrysler, C., Nalpathamkalam, T., Pellecchia, G., Liu, Y., Gazzellone, M. J., D'Abate, L., Deneault, E., Howe, J. L., Liu, R. S., Thompson, A., Zarrei, M., Uddin, M., Marshall, C. R., . . . Scherer, S. W. (2015). Whole-genome sequencing of quartet families with autism spectrum disorder. Nat Med, 21(2), 185-191. https://doi.org/10.1038/nm.3792

Zeidan, J., Fombonne, E., Scorah, J., Ibrahim, A., Durkin, M. S., Saxena, S., Yusuf, A., Shih, A., & Elsabbagh, M. (2022). Global prevalence of autism: A systematic review update. Autism Res, 15(5), 778-790. https://doi.org/10.1002/aur.2696

Zumeta, R. O., Zirkel, P. A., & Danielson, L. J. T. i. L. D. (2014). Identifying specific learning disabilities: Legislation, regulation, and court decisions. 34(1), 8-24.

Al-Mahrezi, A., Al-Futaisi, A., & Al-Mamari, W. (2016). Learning Disabilities: Opportunities and challenges in Oman. Sultan Qaboos Univ Med J, 16(2), e129-131. https://doi.org/10.18295/squmj.2016.16.02.001

Arya, R., Kabra, M., & Gulati, S. (2011). Epilepsy in children with Down syndrome. Epileptic Disord, 13(1), 1-7. https://doi.org/10.1684/epd.2011.0415

Ashwal, S., Russman, B. S., Blasco, P. A., Miller, G., Sandler, A., Shevell, M., & Stevenson, R. (2004). Practice parameter: diagnostic assessment of the child with cerebral palsy: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology, 62(6), 851-863. https://doi.org/10.1212/01.wnl.0000117981.35364.1b

Baburamani, A. A., Patkee, P. A., Arichi, T., & Rutherford, M. A. (2019). New approaches to studying early brain development in Down syndrome. Dev Med Child Neurol, 61(8), 867-879. https://doi.org/10.1111/dmcn.14260

Bai, D., Yip, B. H. K., Windham, G. C., Sourander, A., Francis, R., Yoffe, R., Glasson, E., Mahjani, B., Suominen, A., Leonard, H., Gissler, M., Buxbaum, J. D., Wong, K., Schendel, D., Kodesh, A., Breshnahan, M., Levine, S. Z., Parner, E. T., Hansen, S. N., . . . Sandin, S. (2019). Association of Genetic and Environmental Factors With Autism in a 5-Country Cohort. JAMA Psychiatry, 76(10), 1035-1043. https://doi.org/10.1001/jamapsychiatry.2019.1411

Bauman, M. L., & Kemper, T. L. (2003). The neuropathology of the autism spectrum disorders: what have we learned? Novartis Found Symp, 251, 112-122; discussion 122-118, 281-197.

Bax, M., Goldstein, M., Rosenbaum, P., Leviton, A., Paneth, N., Dan, B., Jacobsson, B., & Damiano, D. (2005). Proposed definition and classification of cerebral palsy, April 2005. Dev Med Child Neurol, 47(8), 571-576. https://doi.org/10.1017/s001216220500112x

Bosanquet, M., Copeland, L., Ware, R., & Boyd, R. (2013). A systematic review of tests to predict cerebral palsy in young children. Dev Med Child Neurol, 55(5), 418-426. https://doi.org/10.1111/dmcn.12140

de Sola, S., de la Torre, R., Sánchez-Benavides, G., Benejam, B., Cuenca-Royo, A., Del Hoyo, L., Rodríguez, J., Catuara-Solarz, S., Sanchez-Gutierrez, J., Dueñas-Espin, I., Hernandez, G., Peña-Casanova, J., Langohr, K., Videla, S., Blehaut, H., Farre, M., & Dierssen, M. (2015). A new cognitive evaluation battery for Down syndrome and its relevance for clinical trials. Front Psychol, 6, 708. https://doi.org/10.3389/fpsyg.2015.00708

DiGuiseppi, C., Hepburn, S., Davis, J. M., Fidler, D. J., Hartway, S., Lee, N. R., Miller, L., Ruttenber, M., & Robinson, C. (2010). Screening for autism spectrum disorders in children with Down syndrome: population prevalence and screening test characteristics. J Dev Behav Pediatr, 31(3), 181-191. https://doi.org/10.1097/DBP.0b013e3181d5aa6d

El Hajj, N., Dittrich, M., Böck, J., Kraus, T. F., Nanda, I., Müller, T., Seidmann, L., Tralau, T., Galetzka, D., & Schneider, E. J. E. (2016). Epigenetic dysregulation in the developing Down syndrome cortex. 11(8), 563-578.

Eliasson, A. C., & Holmefur, M. (2015). The influence of early modified constraint-induced movement therapy training on the longitudinal development of hand function in children with unilateral cerebral palsy. Dev Med Child Neurol, 57(1), 89-94. https://doi.org/10.1111/dmcn.12589

Elkamil, A. I., Andersen, G. L., Hägglund, G., Lamvik, T., Skranes, J., & Vik, T. (2011). Prevalence of hip dislocation among children with cerebral palsy in regions with and without a surveillance programme: a cross sectional study in Sweden and Norway. BMC Musculoskelet Disord, 12, 284. https://doi.org/10.1186/1471-2474-12-284

Elsabbagh, M., Divan, G., Koh, Y. J., Kim, Y. S., Kauchali, S., Marcín, C., Montiel-Nava, C., Patel, V., Paula, C. S., Wang, C., Yasamy, M. T., & Fombonne, E. (2012). Global prevalence of autism and other pervasive developmental disorders. Autism Res, 5(3), 160-179. https://doi.org/10.1002/aur.239

Foster, N. E., Doyle-Thomas, K. A., Tryfon, A., Ouimet, T., Anagnostou, E., Evans, A. C., Zwaigenbaum, L., Lerch, J. P., Lewis, J. D., & Hyde, K. L. (2015). Structural Gray Matter Differences During Childhood Development in Autism Spectrum Disorder: A Multimetric Approach. Pediatr Neurol, 53(4), 350-359. https://doi.org/10.1016/j.pediatrneurol.2015.06.013

Francks, C., MacPhie, I. L., & Monaco, A. P. J. T. L. N. (2002). The genetic basis of dyslexia. 1(8), 483-490.

Frewer, V., Gilchrist, C. P., Collins, S. E., Williams, K., Seal, M. L., Leventer, R. J., & Amor, D. J. (2021). A systematic review of brain MRI findings in monogenic disorders strongly associated with autism spectrum disorder. J Child Psychol Psychiatry, 62(11), 1339-1352. https://doi.org/10.1111/jcpp.13510

Fried, P. A., Watkinson, B., Siegel, L. S. J. N., & teratology. (1997). Reading and language in 9-to 12-year olds prenatally exposed to cigarettes and marijuana. 19(3), 171-183.

Galaburda, A. M., Menard, M. T., & Rosen, G. D. J. P. o. t. N. A. o. S. (1994). Evidence for aberrant auditory anatomy in developmental dyslexia. 91(17), 8010-8013.

Galaburda, A. M., Sherman, G. F., Rosen, G. D., Aboitiz, F., Geschwind, N. J. A. o. N. O. J. o. t. A. N. A., & Society, t. C. N. (1985). Developmental dyslexia: four consecutive patients with cortical anomalies. 18(2), 222-233.

Guedj, F., Pennings, J. L., Massingham, L. J., Wick, H. C., Siegel, A. E., Tantravahi, U., & Bianchi, D. W. (2016). An Integrated Human/Murine Transcriptome and Pathway Approach To Identify Prenatal Treatments For Down Syndrome. Sci Rep, 6, 32353. https://doi.org/10.1038/srep32353

Gupta, M., Dhanasekaran, A. R., & Gardiner, K. J. (2016). Mouse models of Down syndrome: gene content and consequences. Mamm Genome, 27(11-12), 538-555. https://doi.org/10.1007/s00335-016-9661-8

Hebebrand, M., Hüffmeier, U., Trollmann, R., Hehr, U., Uebe, S., Ekici, A. B., Kraus, C., Krumbiegel, M., Reis, A., Thiel, C. T., & Popp, B. (2019). The mutational and phenotypic spectrum of TUBA1A-associated tubulinopathy. Orphanet J Rare Dis, 14(1), 38. https://doi.org/10.1186/s13023-019-1020-x

Jokiranta-Olkoniemi, E., Cheslack-Postava, K., Sucksdorff, D., Suominen, A., Gyllenberg, D., Chudal, R., Leivonen, S., Gissler, M., Brown, A. S., & Sourander, A. (2016). Risk of Psychiatric and Neurodevelopmental Disorders Among Siblings of Probands With Autism Spectrum Disorders. JAMA Psychiatry, 73(6), 622-629. https://doi.org/10.1001/jamapsychiatry.2016.0495

Kemper, T. L. (1985). Anatomical basis of learning disabilities. Brain specialization. Otolaryngol Clin North Am, 18(2), 305-314.

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