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Saudi Medical Journal|January 1, 2015
Epidemiology of neural tube defectsMohammed Z Seidahmed, Omar B Abdelbasit, Meeralebbae M Shaheed, et al.
Orphanet Journal of Rare Diseases|May 3, 2020
The natural history of infantile neuroaxonal dystrophyFadie D Altuame, Gretchen Foskett, Paldeep S Atwal, et al.
Saudi Medical Journal|January 1, 2015
Genetic, chromosomal, and syndromic causes of neural tube defectsMohammed Z Seidahmed, Omer B Abdelbasit, Meeralebbae M Shaheed, et al.
Paediatrics and International Child Health|June 23, 2016
Auto-immune anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis: three case reportsFahad A Bashiri, Abdulrahman A Al-Rasheed, Saeed M Hassan, et al.
Saudi Medical Journal|March 15, 2006
Infectious and inflammatory disorders of the circulatory system as risk factors for stroke in Saudi childrenMustafa A Salih, Abdel-Galil M Abdel-Gader, Ahmed A Al-Jarallah, et al.
Gene|December 24, 2013
C19orf12 mutation leads to a pallido-pyramidal syndromeMichael C Kruer, Mustafa A Salih, Catherine Mooney, et al.
Human Mutation|June 14, 2012
Molecular characterization of Joubert syndrome in Saudi ArabiaAnas M Alazami, Muneera J Alshammari, Mustafa A Salih, et al.
BMC Neurology|May 27, 2020
Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15)Mohammed Z Seidahmed, Muddathir H Hamad, Albandary AlBakheet, et al.
American Journal of Medical Genetics. Part A|January 11, 2016
Novel copy number variants and major limb reduction malformation: Report of three casesHanan E Shamseldin, Shams Anazi, Salma M Wakil, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
The clinical spectrum of homozygous HOXA1 mutationsThomas M Bosley, Ibrahim A Alorainy, Mustafa A Salih, et al.
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