Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Mohammed Z. Seidahmed"'
Autor:
Amira Oshi, Abdullah Alfaifi, Mohammed Z. Seidahmed, Khalid Al Hussein, Abeer Miqdad, Abdelmohsin Samadi, Omar Abdelbasit
Publikováno v:
Clinical Case Reports, Vol 9, Iss 3, Pp 1295-1298 (2021)
Abstract GABA transaminase deficiency should be considered in the differential diagnosis of early onset epileptic encephalopathies. This case was diagnosed post‐mortem, but increased vigilance to this will allow for earlier diagnoses in other infan
Externí odkaz:
https://doaj.org/article/03cd9a936bd044e8a683739f119912c6
Autor:
Mohammed Z. Seidahmed, Muddathir H. Hamad, Albandary AlBakheet, Salah A. Elmalik, Abdulmajeed AlDrees, Jumanah Al-Sufayan, Ibrahim Alorainy, Ibrahim M. Ghozzi, Dilek Colak, Mustafa A. Salih, Namik Kaya
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-7 (2020)
Abstract Background Homozygous frameshift mutation in RUBCN (KIAA0226), known to result in endolysosomal machinery defects, has previously been reported in a single Saudi family with autosomal recessive spinocerebellar ataxia (Salih ataxia, SCAR15, O
Externí odkaz:
https://doaj.org/article/86ab0932971e4299ae92f7927c76a1f0
Autor:
Mustafa A. Salih, Mohammed Z. Seidahmed, Heba Y. El Khashab, Muddathir H. Hamad, Thomas M. Bosley, Sabrina Burn, Angela Myers, Megan L. Landsverk, Patricia L. Crotwell, Kaya Bilguvar, Shrikant Mane, Michael C. Kruer
Publikováno v:
Tremor and Other Hyperkinetic Movements, Vol 5 (2015)
Background: The etiology of many cases of childhood-onset chorea remains undetermined, although advances in genomics are revealing both new disease-associated genes and variant phenotypes associated with known genes. Methods: We report a Saudi family
Externí odkaz:
https://doaj.org/article/a4dfd5789c5648738246a332b1f88dac
Autor:
Ghada I. Aboheimed, Maha M. AlRasheed, Sultan Almudimeegh, Karla A. Peña-Guerra, Kelly J. Cardona-Londoño, Mustafa A. Salih, Mohammed Z. Seidahmed, Futwan Al-Mohanna, Dilek Colak, Robert J. Harvey, Kirsten Harvey, Stefan T. Arold, Namik Kaya, Arnaud J. Ruiz
Publikováno v:
The Journal of biological chemistry. 298(7)
Hyperekplexia is a rare neurological disorder characterized by exaggerated startle responses affecting newborns with the hallmark characteristics of hypertonia, apnea, and noise or touch-induced nonepileptic seizures. The genetic causes of the diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::258eb5a9ef5e931d9ac67affd2bb6c44
https://pubmed.ncbi.nlm.nih.gov/35526563
https://pubmed.ncbi.nlm.nih.gov/35526563
Autor:
Mohammed Z, Seidahmed, Omer B, Abdelbasit, Meeralebbae M, Shaheed, Khalid A, Alhussein, Abeer M, Miqdad, Abdulmohsen S, Samadi, Mohammed I, Khalil, Elham, Al-Mardawi, Mustafa A, Salih
Publikováno v:
Saudi Medical Journal
Objective: To ascertain the incidence, and describe the various forms of neural tube defects (NTDs) due to genetic, chromosomal, and syndromic causes. Methods: We carried out a retrospective analysis of data retrieved from the medical records of newb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b248cb9226500c287b2208d6671283d8
https://pubmed.ncbi.nlm.nih.gov/25551112
https://pubmed.ncbi.nlm.nih.gov/25551112
Autor:
Abeer E, Lasheen, Omer B, Abdelbasit, Mohammed Z, Seidahmed, Khalid A, Hussein, Abeer M, Miqdad, Mohammed H, Al Zahrani, Gehan M, Farid, Haitham A, Badr
Publikováno v:
Saudi medical journal. 35(6)
To determine the outcome of infants born to diabetic mothers at Security Forces Hospital, Riyadh, Saudi Arabia, and compare the complications seen in these infants with infants of non-diabetic mothers.This is a concurrent prospective cohort study of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85445ed8e049fe0f0057b4d5eb5cd417
https://pubmed.ncbi.nlm.nih.gov/24888656
https://pubmed.ncbi.nlm.nih.gov/24888656
Publikováno v:
Saudi medical journal. 30(2)
Fetal valproate syndrome (FVS) is a well-recognized constellation of dysmorphic features, and neurodevelopmental retardation that results from prenatal exposure to the anticonvulsant valproic acid. In this report, we describe a case with typical feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e5bdc6968241f967da00dd2a4792948
https://pubmed.ncbi.nlm.nih.gov/19618023
https://pubmed.ncbi.nlm.nih.gov/19618023