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Neurosciences (Riyadh, Saudi Arabia)|February 5, 2013
Hallervorden-Spatz syndrome. Variable imaging findingsGhada M Abdel-Salam, Maha S ZakiNeurosciences (Riyadh, Saudi Arabia)|January 24, 2012
Clinical spectrum associated with some structural cerebellar abnormalitiesGhada M Abdel-Salam, Marwa I Shahab, Amany H Galal, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|October 30, 2020
A founder mutation in PEX12 among Egyptian patients in peroxisomal biogenesis disorderMaha S Zaki, Mahmoud Y Issa, Manal M Thomas, et al.Nature Genetics|April 8, 2015
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunctionNaiara Akizu, Vincent Cantagrel, Maha S Zaki, et al.American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.Pageof 1