Serebral Folat Eksikliği ve Folat Reseptörü Otoimmünitesi

Avşar AF, Kaya S, Kaya B. Türkiye’de Folik Asit Perikonsepsiyonel Olarak Kullanılmalı Mıdır? Ankara Medical Journal. 2012;12(4):188-194.

Baykan M, Gençpınar M. Serebral Folat Eksikliği ve Folat Reseptörü Otoimmünitesi. Türkiye Klinikleri.2023; 5(1): 195-200

Ramaekers V, Jeffrey M. Clinical Recognition And Aspects Of The Cerebral Folate Deficiency Syndromes. Clin Chem Lab Med. 2013; 51(3): 497–511. doi 10.1515/cclm-2012-0543

Medlink. Beyin folat eksikliği 2024. (29/10/2024 tarihinde https://www.medlnk.com/artcles/cerebral-folate-defcency adresinden ulaşılmıştır).

OMIM. Megaloblastic Anemia Due To Dihydrofolate Reductase Deficiency 2011. (30/10/2024 tarihinde https://omm.org/entry/613839 adresinden ulaşılmıştır.)

Holger C, Desire´e E.C., Henk B. et al. Dihydrofolate Reductase Deficiency Due to a Homozygous DHFR Mutation Causes Megaloblastic Anemia and Cerebral Folate Deficiency Leading to Severe Neurologic Disease. The American Journal of Human Genetics 2011(88):226-231.

Ramaekers VT, Quadros EV. Cerebral Folate Deficiency Syndrome: Early Diagnosis, Intervention and Treatment Strategies. Nutrients. 2022; 28;14(15):3096. doi: 10.3390/nu14153096.

Amerika Birleşik Devletleri Ulusal Tıp Kütüphanesi. MTHFR geni. MedilinePlus. 2019. (29/10/2024 tarihinde https://medlineplus.gov/genetics/gene/mthfr/#conditions adresinden ulaşılmıştır.)

Myint SM, Sun LY. L-serine: Neurologial Effects and Therapeutic Potantial. Pubmed 2023;11(8):2117 doi: 10.3390/biomedicines11082117

Wallace SE. GeneReviews Resource Materials. 2018 Feb 12 (Updated 2023 Dec 7). In: Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews. Seattle (WA): University of Washington, Seattle; 1993-2024.

Geller J, Kronn D. Jayabose S. et al. Hereditary Folate Malabsorption: Family Report and Literature Review. Medicine 2002 81(1):s 51-68

Amerika Birleşik Devletleri Ulusal Tıp Kütüphanesi. Hereditary folate malabsortion. MedilinePlus.2024.(30/10/2024 tarihinde https://medlneplus.gov/genetcs/condton/heredtary-folate-malabsorpton/#causes 4/ adresinden alınmıştır).

Bobrowski-Khoury N, Ramaekers VT, Sequeira JM, Quadros EV. Folate Receptor Alpha Autoantibodies in Autism Spectrum Disorders: Diagnosis, Treatment and Prevention Personalized Medicine 2021; 11(8):710. doi: org/10.3390/jpm11080710

Amerika Birleşik Devletleri Ulusal Tıp Kütüphanesi. Serebral folate transport ben. MedilinePlus.2019 (30/10/2024 tarihinde https://medlineplus.gov/genetics/condition/cerebral-folate-transport-deficiency/ adresinden alınmıştır).

Sequeira, Jeffrey M., Ramaekers, Vincent Th. and Quadros, Edward V.. The diagnostic utility of folate receptor autoantibodies in blood. Clinical Chemistry and Laboratory Medicine, vol. 51, no. 3, 2013,545-554. https://doi.org/10.1515/cclm-2012-0577,

Vincent P. Folate deficiency. Patient 2024.(30/10/2024 tarihinde https://patent.nfo/doctor/folate-defcency adresinden alınmıştır).

Frye RE., Rossignol DA., Scahill L. et al. Treatment of folate metabolism abnormalities in autism spectrum disorder. ScinceDirect 2020. Pediatric Neurology Seminars 2020(35):1-18.

Frye, R., Slattery, J., Delhey, L. et al. Folinic acid improves verbal communication in children with autism and language impairment: a randomized double-blind placebo-controlled trial. Mol Psychiatry 23, 247–256 (2018). https://doi.org/10.1038/mp.2016.168

O'Ferrall E. Mitochondrial myopathies: Treatment. Uptodate 2024.(30/10/2024 tarihinde https://medilib.ir/uptodate/show/5149 adresinden alınmıştır).

Bölükbaşı, N. Antiepileptik ilaçların tiroid hormon düzeyleri ve serum biyokimyasına etkileri (SAE-09008 kodlu proje). Adnan Menderen Üniversitesi Ssağlık Bilimleri Enstitüsü Farmakoloji ve Toksikoloji Anabilim Dalı. Danışman: Prof. Dr. Ferda Akar. 2009