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1. Autoantibodies to neuronal antigens in children with new‐onset seizures classified according to the revised ILAE organization of seizures and epilepsies. Issue 12 (23rd October 2013)

4. Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy. Issue 3 (19th December 2022)

5. Homozygous loss‐of‐function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies. Issue 11 (22nd July 2019)

6. Pediatric Multiple Sclerosis in the United Arab Emirates: Characteristics From a Multicenter Study and Global Comparison. (May 2018)

7. Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency. Issue 18 (5th May 2022)

9. VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features. Issue 4 (26th December 2019)