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M. S. Rashed

Observed names: M Rashed, M S Rashed, M. Rashed, M. Salah El-Din Rashed, M.S. Rashed
OpenAlex ID: A5110036909
Newborn screening: Experiences in the Middle East and North Africa
2007 · A. A. Saadallah, M. S. Rashed · Journal of Inherited Metabolic Disease · 105
The T/G−13915 variant upstream of the lactase gene ( LCT ) is the founder allele of lactase persistence in an urban Saudi population
2007 · F Imtiaz, E Savilahti, et al. · Journal of Medical Genetics · 103
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Hepatic protein arylation, glutathione depletion, and metabolite profiles of acetaminophen and a non-hepatotoxic regioisomer, 3'-hydroxyacetanilide, in the mouse.
1990 · M S Rashed, T G Myers, et al. · Drug Metabolism and Disposition · 71
Unusual presentations of propionic acidemia
1994 · P.T. Ozand, M. Rashed, et al. · Brain and Development · 64
Electrospray tandem mass spectrometry in the diagnosis of organic acidemias
1994 · M. S. Rashed, P. T. Ozand, et al. · Rapid Communications in Mass Spectrometry · 60
Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy
1994 · P.T. Ozand, M. Rashed, et al. · Brain and Development · 49
4-Hydroxybutyric aciduria
1994 · Z. Rahbeeni, P.T. Ozand, et al. · Brain and Development · 42
Infectious complications of propionic acidemia in Saudia Arabia
1998 · M. Al. Essa, Z. Rahbeeni, et al. · Clinical Genetics · 35
Quantification of N‐acetylaspartic acid in urine by LC‐MS/MS for the diagnosis of Canavan disease
2007 · O. Y. Al‐Dirbashi, M. S. Rashed, et al. · Journal of Inherited Metabolic Disease · 26
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency
2005 · M.Z. Seidahmed, E.A. Alyamani, et al. · American Journal of Medical Genetics Part A · 23
Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria
2005 · M. Al‐Sayed, S. AlAhmed, et al. · Journal of Inherited Metabolic Disease · 18
Carnitine‐acylcarnitine translocase deficiency is a treatable disease
1999 · A. I. Al Aqeel, M. S. Rashed, et al. · Journal of Inherited Metabolic Disease · 17
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Zeliweger Syndrome in Saudi Arabia and Its Distinct Features
1999 · M. Al-Essa, Gursev S. Dhaunsi, et al. · Clinical Pediatrics · 16
Isovaleric acidemia appearing as diabetic ketoacidosis
1996 · N. Attia, N. Sakati, et al. · Journal of Inherited Metabolic Disease · 15
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 gene
2007 · O. Y. Al‐Dirbashi, K. K. Abu‐Amero, et al. · Journal of Inherited Metabolic Disease · 14
Investigations of the N-hydroxylation of 3'-hydroxyacetanilide, a non-hepatotoxic positional isomer of acetaminophen.
1989 · M S Rashed, A J Streeter, et al. · Drug Metabolism and Disposition · 14
Application of PMR Spectroscopy in Pharmaceutical Analysis Assay of Furosemide
1979 · Hassan Y. Aboul-enein, A. A. Al-badr, et al. · Spectroscopy Letters · 8
Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic response
1999 · M. A. Al Essa, M. S. Rashed, et al. · Eastern Mediterranean Health Journal · 4
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Classic homocystinuria: clinical, biochemical and radiological observations, and therapeutic outcome of 24 Saudi patients
1999 · M. A. Al Essa, M. S. Rashed, et al. · Eastern Mediterranean Health Journal · 3
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Cholinergic activity of fluorinated quaternary pilocarpine derivatives†
1986 · Hassan Y. Aboul‐Enein, A. A. Al‐Badr, et al. · Toxicological & Environmental Chemistry Reviews · 2
6-Pyruvoyltetrahydropterin synthase deficiency diagnosed in tandem mass spectrometry-based newborn screening
1998 · M. Al Essa, P. T. Ozand, et al. · Eastern Mediterranean Health Journal
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[Diagnosis of organic aciduria].
1995 · L García, P Ozand, et al. · PubMed
Works count: 22
Citation count: 689
H-index: 14
I10-index: 16
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