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Journal of Neurology|February 26, 2008
Spinocerebellar ataxia type 2 (SCA2) in an Egyptian family presenting with polyphagia and marked CAG expansion in infancyAlice Abdel-Aleem, Maha S ZakiNeurosciences (Riyadh, Saudi Arabia)|February 5, 2013
Hallervorden-Spatz syndrome. Variable imaging findingsGhada M Abdel-Salam, Maha S ZakiBMC Research Notes|April 18, 2023
Abnormal expression of lysosomal glycoproteins in patients with congenital disorders of glycosylationSahar Sabry, Noura R Eissa, Maha S ZakiBrain & Development|March 28, 2006
Isolated Dandy-Walker malformation associated with brain stem dysgenesis in male sibsGhada M H Abdel-Salam, Marwa Shehab, Maha S ZakiAmerican Journal of Medical Genetics. Part A|March 18, 2011
Congenital isolated leukonychia totalis in three Egyptian sibsHanan H Afifi, Mahmoud F Abdel-Hamid, Maha S ZakiJournal of Human Genetics|November 28, 2023
A missense variant in EXOSC8 causes exon skipping and expands the phenotypic spectrum of pontocerebellar hypoplasia type 1CMaha S Zaki, Sherif F Abdel-Ghafar, Mohamed S Abdel-HamidAmerican Journal of Medical Genetics. Part A|October 18, 2011
Co-occurrence of distinct ciliopathy diseases in single families suggests genetic modifiersMaha S Zaki, Shifteh Sattar, Rustin A Massoudi, et al.American Journal of Medical Genetics. Part A|July 18, 2009
Familial congenital unilateral cerebral ventriculomegaly: Delineation of a distinct genetic disorderMaha S Zaki, Hanan H Afifi, A J Barkovich, et al.Clinical Dysmorphology|June 7, 2007
Adams-Oliver syndrome: further evidence of an autosomal recessive variantSamia A Temtamy, Mona S Aglan, Adel M Ashour, et al.American Journal of Medical Genetics. Part A|June 26, 2015
Dandy-Walker malformation, genitourinary abnormalities, and intellectual disability in two familiesMaha S Zaki, Amira Masri, Anne Gregor, et al.Pageof 25