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Clinical Chemistry|August 1, 1995
Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bileM S Rashed, P T Ozand, M J Bennett, et al.Biochemical and Biophysical Research Communications|January 15, 1990
S-(N-methylcarbamoyl)glutathione: a reactive S-linked metabolite of methyl isocyanateP G Pearson, J G Slatter, M S Rashed, et al.Archives of Disease in Childhood|December 22, 2000
A severe genotype with favourable outcome in very long chain acyl-CoA dehydrogenase deficiencyE H Touma, M S Rashed, C Vianey-Saban, et al.Journal of Medicinal Chemistry|May 1, 1984
Phosphorus analogues of gamma-aminobutyric acid, a new class of anticonvulsantsL A Cates, V S Li, C C Yakshe, et al.Clinical Chemistry|July 1, 1997
Screening blood spots for inborn errors of metabolism by electrospray tandem mass spectrometry with a microplate batch process and a computer algorithm for automated flagging of abnormal profilesM S Rashed, M P Bucknall, D Little, et al.Journal of Inherited Metabolic Disease|November 1, 2002
Identification of two novel mutations in OCTN2 from two Saudi patients with systemic carnitine deficiencyZ Rahbeeni, F M Vaz, K Al-Hussein, et al.Journal of Inherited Metabolic Disease|August 19, 2007
LC-MS/MS determination of dibasic amino acids for the diagnosis of cystinuria. Application in a family affected by a novel splice-acceptor site mutation in the SLC7A9 geneO Y Al-Dirbashi, K K Abu-Amero, A F Alswaid, et al.Journal of Medicinal Chemistry|March 1, 1980
Cyclophosphamide potentiation and aldehyde oxidase inhibition by phosphorylated aldehydes and acetalsL A Cates, G S Jones, D J Good, et al.Clinical Genetics|September 4, 1998
Infectious complications of propionic acidemia in Saudia ArabiaM Al Essa, Z Rahbeeni, S Jumaah, et al.Saudi Medical Journal|December 18, 2001
Carnitine palmityl transferase I deficiencyA I Al-Aqeel, M S Rashed, J P Ruiter, et al.Pageof 6