M. Z. Seidahmed

Most-cited papers

Epidemiology of neural tube defects
M. Z. Seidahmed, O. Abdelbasit, M. Shaheed, K. Alhussein +4 more
2015Saudi Medical Journal261 citations Open access
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Epidemiology, prenatal management, and prevention of neural tube defects
M. Salih, W. Murshid, M. Z. Seidahmed
2014Saudi Medical Journal66 citations
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Brain Stem and Cerebellar Findings in Joubert Syndrome
I. Alorainy, S. Sabir, M. Z. Seidahmed, Hamid A Farooqu +1 more
2006Journal of computer assisted tomography49 citations
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Classification, clinical features, and genetics of neural tube defects
M. Salih, W. Murshid, M. Z. Seidahmed
2014Saudi Medical Journal48 citations
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Report of a case of Raine syndrome and literature review
M. Z. Seidahmed, A. Alazami, O. B. Abdelbasit, K. Alhussein +5 more
2015American Journal of Medical Genetics. Part A23 citations
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Sirenomelia and severe caudal regression syndrome
M. Z. Seidahmed, O. B. Abdelbasit, K. Alhussein, A. Miqdad +2 more
2014Saudi Medical Journal23 citations
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Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15)
M. Z. Seidahmed, Muddathir H. A. Hamad, Albandary Albakheet, S. Elmalik +7 more
2020BMC Neurology17 citations Open access
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Neurologic Injury in Isolated Sulfite Oxidase Deficiency
T. Bosley, I. Alorainy, D. Oystreck, A. Hellani +7 more
2014Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques17 citations Open access
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A case of fetal valproate syndrome with new features expanding the phenotype.
M. Z. Seidahmed, A. Miqdad, Hessa S Al-Dohami, O. Shareefi
2009Saudi Medical Journal14 citations
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Infants of diabetic mothers. A cohort study.
Abeer E Lasheen, O. B. Abdelbasit, M. Z. Seidahmed, K. Hussein +4 more
2014Saudi Medical Journal13 citations
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Genetic, chromosomal, and syndromic causes of neural tube defects
M. Z. Seidahmed, O. B. Abdelbasit, M. Shaheed, K. Alhussein +5 more
2014Saudi Medical Journal12 citations
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A novel syndrome of lethal familial hyperekplexia associated with brain malformation
M. Z. Seidahmed, M. Salih, Omer B. Abdulbasit, M. Shaheed +6 more
2012BMC Neurology12 citations Open access
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Gonadal mosaicism for ACTA1 gene masquerading as autosomal recessive nemaline myopathy
M. Z. Seidahmed, Mustafa A. Salih, O. B. Abdelbasit, A. Alassiri +7 more
2016American Journal of Medical Genetics. Part A10 citations
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Clinical, genetic, and functional characterization of the glycine receptor β-subunit A455P variant in a family affected by hyperekplexia syndrome
Ghada I. Aboheimed, Maha M. Alrasheed, Sultan Almudimeegh, Karla A. Peña-Guerra +10 more
2022Journal of Biological Chemistry5 citations Open access
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GABA transaminase deficiency. Case report and literature review
A. Oshi, Abdullah Alfaifi, M. Z. Seidahmed, K. Alhussein +3 more
2021Clinical Case Reports5 citations Open access
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Founder mutation in RUBCN gene in a second family confirms Salih ataxia (scar15)
M. Salih, Muddathir H. A. Hamad, M. Z. Seidahmed, A. BinBakheet +2 more
2019Journal of Neurological Sciences1 citations
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The Clinical Presentation of Reversible Cardiomyopathy and Left Ventricular Noncompaction
A. Oshi, O. Abdelbasit, M. Z. Seidahmed, K. Hussein +6 more
2021New Frontiers in Medicine and Medical Research Vol. 130 citations
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The ethics of lethal congenital malformations. Is palliative therapy possible?
O. B. Abdelbasit, M. Z. Seidahmed, K. Alhussein, A. Miqdad +4 more
2019Journal of Clinical Neonatology0 citations
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A case of reversible cardiomyopathy & left ventricular noncompaction
O. Amira, Abdelbasit, M. Z. Seidahmed, K. Hussein +5 more
20160 citations Open access
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