نقص الفوليك الدماغي (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "نقص الفوليك الدماغي" in Arabic language version.

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archive.org

Gordon، N (2009). "Cerebral folate deficiency". Developmental Medicine and Child Neurology. ج. 51 ع. 3: 180–182. DOI:10.1111/j.1469-8749.2008.03185.x. PMID:19260931.

books.google.com

Phillip L. Pearl, MD (4 أكتوبر 2012). Inherited Metabolic Epilepsies. Demos Medical Publishing. ص. 3–. ISBN:978-1-61705-056-5. مؤرشف من الأصل في 2020-01-27.

doi.org

Gordon، N (2009). "Cerebral folate deficiency". Developmental Medicine and Child Neurology. ج. 51 ع. 3: 180–182. DOI:10.1111/j.1469-8749.2008.03185.x. PMID:19260931.
"Genetic causes of cerebral folate deficiency: clinical, biochemical and therapeutic aspects". Drug Discovery Today. ج. 17 ع. 23–24: 1299–1306. 2012. DOI:10.1016/j.drudis.2012.07.008. PMID:22835503.
Baumgartner، MR (2013). Vitamin-responsive disorders: cobalamin, folate, biotin, vitamins B1 and E. ج. 113. ص. 1799–1810. DOI:10.1016/B978-0-444-59565-2.00049-6. ISBN:9780444595652. PMID:23622402. {{استشهاد بكتاب}}: |عمل= تُجوهل (مساعدة)
"Cerebral folate deficiency". Journal of Inherited Metabolic Disease. ج. 33 ع. 5: 563–570. 2010. DOI:10.1007/s10545-010-9159-6. PMID:20668945.
"Vitamin-responsive epileptic encephalopathies in children". Epilepsy Research and Treatment. ج. 2013: 1–8. 2013. DOI:10.1155/2013/510529. PMC:3745849. PMID:23984056.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption". Molecular Aspects of Medicine. ج. 53: 57–72. 2017. DOI:10.1016/j.mam.2016.09.002. PMC:5253092. PMID:27664775.
"The metabolic basis for developmental disorders due to defective folate transport". Biochimie. ج. 126: 31–42. 2016. DOI:10.1016/j.biochi.2016.02.012. PMID:26924398.

medlineplus.gov

"Cerebral folate transport deficiency". Genetics Home Reference. مؤرشف من الأصل في 2019-04-13. اطلع عليه بتاريخ 2019-01-07.

nih.gov

pubmed.ncbi.nlm.nih.gov

Gordon، N (2009). "Cerebral folate deficiency". Developmental Medicine and Child Neurology. ج. 51 ع. 3: 180–182. DOI:10.1111/j.1469-8749.2008.03185.x. PMID:19260931.
"Genetic causes of cerebral folate deficiency: clinical, biochemical and therapeutic aspects". Drug Discovery Today. ج. 17 ع. 23–24: 1299–1306. 2012. DOI:10.1016/j.drudis.2012.07.008. PMID:22835503.
Baumgartner، MR (2013). Vitamin-responsive disorders: cobalamin, folate, biotin, vitamins B1 and E. ج. 113. ص. 1799–1810. DOI:10.1016/B978-0-444-59565-2.00049-6. ISBN:9780444595652. PMID:23622402. {{استشهاد بكتاب}}: |عمل= تُجوهل (مساعدة)
"Cerebral folate deficiency". Journal of Inherited Metabolic Disease. ج. 33 ع. 5: 563–570. 2010. DOI:10.1007/s10545-010-9159-6. PMID:20668945.
"Vitamin-responsive epileptic encephalopathies in children". Epilepsy Research and Treatment. ج. 2013: 1–8. 2013. DOI:10.1155/2013/510529. PMC:3745849. PMID:23984056.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption". Molecular Aspects of Medicine. ج. 53: 57–72. 2017. DOI:10.1016/j.mam.2016.09.002. PMC:5253092. PMID:27664775.
"The metabolic basis for developmental disorders due to defective folate transport". Biochimie. ج. 126: 31–42. 2016. DOI:10.1016/j.biochi.2016.02.012. PMID:26924398.

ncbi.nlm.nih.gov

"Vitamin-responsive epileptic encephalopathies in children". Epilepsy Research and Treatment. ج. 2013: 1–8. 2013. DOI:10.1155/2013/510529. PMC:3745849. PMID:23984056.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption". Molecular Aspects of Medicine. ج. 53: 57–72. 2017. DOI:10.1016/j.mam.2016.09.002. PMC:5253092. PMID:27664775.

rarediseases.info.nih.gov

"Cerebral folate deficiency". rarediseases.info.nih.gov. مؤرشف من الأصل في 2019-01-08. اطلع عليه بتاريخ 2019-01-07.

web.archive.org

"Cerebral folate deficiency". rarediseases.info.nih.gov. مؤرشف من الأصل في 2019-01-08. اطلع عليه بتاريخ 2019-01-07.
"Cerebral folate transport deficiency". Genetics Home Reference. مؤرشف من الأصل في 2019-04-13. اطلع عليه بتاريخ 2019-01-07.
Phillip L. Pearl, MD (4 أكتوبر 2012). Inherited Metabolic Epilepsies. Demos Medical Publishing. ص. 3–. ISBN:978-1-61705-056-5. مؤرشف من الأصل في 2020-01-27.