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Mohamed Rashed

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Disorders

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Saudi Arabia

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Publications

TOP 3
M Al-Owain; H Bamashmous; A Edrees; Eissa Faqeih; W Garout; Faiqa Imtiaz; B Meyer; Zuhair Rahbeeni; Mohamed S Rashed; Nadia A Sakati; T Shuaib; S Al-Ameer; Mohammed Al-Amoudi; A Al-Hashem; Zuhair N Al-Hassnan; Ali N Al Odaib; J Y Al-Aama
Smith-Lemli-Opitz syndrome among Arabs.
Faiqa Imtiaz; Brian F Meyer; Alya Qari; Zuhair Rahbeeni; Mohamed S Rashed; Zuhair N Al-Hassnan; Rabab Allam; Bashayer Al-Mubarak; Mohammed Al-Owain; Hamad Al-Zaidan; Hanaa El-Karaksy; Moeenaldeen Al-Sayed
Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin.
Faiqa Imtiaz; Moeenaldeen Al-Sayed; Danyah Trabzuni; Bashair R Al-Mubarak; Osama Alsmadi; Mohamed S Rashed; Brian F Meyer
Novel mutations underlying argininosuccinic aciduria in Saudi Arabia.

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All Publications

2012: M Al-Owain; H Bamashmous; A Edrees; Eissa Faqeih; W Garout; Faiqa Imtiaz; B Meyer; Zuhair Rahbeeni; Mohamed S Rashed; Nadia A Sakati; T Shuaib; S Al-Ameer; Mohammed Al-Amoudi; A Al-Hashem; Zuhair N Al-Hassnan; Ali N Al Odaib; J Y Al-Aama
Smith-Lemli-Opitz syndrome among Arabs.
Clinical genetics 2012;82(2):165-72.
2011: Faiqa Imtiaz; Brian F Meyer; Alya Qari; Zuhair Rahbeeni; Mohamed S Rashed; Zuhair N Al-Hassnan; Rabab Allam; Bashayer Al-Mubarak; Mohammed Al-Owain; Hamad Al-Zaidan; Hanaa El-Karaksy; Moeenaldeen Al-Sayed
Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin.
Molecular genetics and metabolism 2011;104(4):688-90.
2010: Faiqa Imtiaz; Moeenaldeen Al-Sayed; Danyah Trabzuni; Bashair R Al-Mubarak; Osama Alsmadi; Mohamed S Rashed; Brian F Meyer
Novel mutations underlying argininosuccinic aciduria in Saudi Arabia.
BMC research notes 2010;3():79.
2009: Osama Y Al-Dirbashi; Wesam Kurdi; Faiqa Imtiaz; Asmahan M Ahmad; Moeenaldeen Al-Sayed; Maha Tulbah; Maha Al-Nemer; Mohamed S Rashed
Reliable prenatal diagnosis of Canavan disease by measuring N-acetylaspartate in amniotic fluid using liquid chromatography tandem mass spectrometry.
Prenatal diagnosis 2009;29(5):477-80.
2008: Osama Y Al-Dirbashi; Mohamed S Rashed; Minnie Jacob; Lujane Y Al-Ahaideb; Mohammed Al-Amoudi; Zuhair Rahbeeni; Moeen M Al-Sayed; Zuhair N Al-Hassnan; Mohamed Al-Owain; Hamad Al-Zeidan
Improved method to determine succinylacetone in dried blood spots for diagnosis of tyrosinemia type 1 using UPLC-MS/MS.
Biomedical chromatography : BMC 2008;22(11):1181-5.
2008: Osama Y Al-Dirbashi; Tomofumi Santa; Mohamed S Rashed; Zuhair Al-Hassnan; Nobuyuki Shimozawa; Aziza Chedrawi; Minnie Jacob; Manhal Al-Mokhadab
Rapid UPLC-MS/MS method for routine analysis of plasma pristanic, phytanic, and very long chain fatty acid markers of peroxisomal disorders.
Journal of lipid research 2008;49(8):1855-62.
2008: Tomofumi Santa; Osama Y Al-Dirbashi; Tomoko Ichibangase; Mohamed S Rashed; Takeshi Fukushima; Kazuhiro Imai
Synthesis of 4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-methylhydrazino-2,1,3-benzoxadiazole (DAABD-MHz) as a derivatization reagent for aldehydes in liquid chromatography/electrospray ionization-tandem mass spectrometry.
Biomedical chromatography : BMC 2008;22(2):115-8.
2008: Zuhair N Al-Hassnan; Mohamed S Rashed; Osama Y Al-Dirbashi; Zoltan Patay; Zuhair Rahbeeni; Khaled K. Abu-Amero
Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.
Journal of the neurological sciences 2008;264(1-2):187-94.
2008: Nabil Sabri Enattah; Tine G K Jensen; Mette Nielsen; Rikke Lewinski; Mikko Kuokkanen; Heli Rasinpera; Hatem El-Shanti; Jeong Kee Seo; Michael Alifrangis; Insaf F Khalil; Abdrazak Natah; Ahmed Ali; Sirajedin Natah; David Comas; S Qasim Mehdi; Leif Groop; Else Marie Vestergaard; Faiqa Imtiaz; Mohamed S Rashed; Brian Meyer; Jesper T Troelsen; Leena Peltonen
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture.
American journal of human genetics 2008;82(1):57-72.
2007: Tomofumi Santa; Osama Y Al-Dirbashi; Tomoko Ichibangase; Takeshi Fukushima; Mohamed S Rashed; Takashi Funatsu; Kazuhiro Imai
Synthesis of benzofurazan derivatization reagents for carboxylic acids in liquid chromatography/electrospray ionization-tandem mass spectrometry.
Biomedical chromatography : BMC 2007;21(11):1207-13.
2007: Faiqa Imtiaz; Erkki Savilahti; Annikki Sarnesto; D Trabzuni; K Al-Kahtani; I Kagevi; Mohamed S Rashed; Brian F Meyer; I Järvelä
The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.
Journal of medical genetics 2007;44(10):e89.
2007: Osama Y Al-Dirbashi; Mohamed S Rashed; Manhal A Al-Mokhadab; Khalid Al-Qahtani; Moeenaldeen Al-Sayed; Wesam Kurdi
Stable isotope dilution analysis of N-acetylaspartic acid in urine by liquid chromatography electrospray ionization tandem mass spectrometry.
Biomedical chromatography : BMC 2007;21(9):898-902.
2007: Amal A A Saadallah; Mohamed S Rashed
Newborn screening: experiences in the Middle East and North Africa.
Journal of inherited metabolic disease 2007;30(4):482-9.
2007: Osama Y Al-Dirbashi; Khaled K. Abu-Amero; Abdulrahman Alswaid; G F Hoffmann; Khalid Al-Qahtani; Mohamed S Rashed
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.
Journal of inherited metabolic disease 2007;30(4):611.
2007: Osama Y Al-Dirbashi; Mohamed S Rashed; Khalid Al-Qahtani; M A Al-Mokhadab; Wesam Kurdi; Moeenaldeen Al-Sayed
Quantification of N-acetylaspartic acid in urine by LC-MS/MS for the diagnosis of Canavan disease.
Journal of inherited metabolic disease 2007;30(4):612.
2007: Moeen Al-Sayed; Saad Al-Hassan; Mohamed S Rashed; Meshal Qeba; Serdar Coskun
Preimplantation genetic diagnosis for Zellweger syndrome.
Fertility and sterility 2007;87(6):1468.e1-3.
2007: Osama Y Al-Dirbashi; Tomofumi Santa; Khalid Al-Qahtani; Mohammed Al-Amoudi; Mohamed S Rashed
Analysis of organic acid markers relevant to inherited metabolic diseases by ultra-performance liquid chromatography/tandem mass spectrometry as benzofurazan derivatives.
Rapid communications in mass spectrometry : RCM 2007;21(13):1984-90.
2006: Osama Y Al-Dirbashi; Zuhair N Al-Hassnan; Mohamed S Rashed
Determination of homocitrulline in urine of patients with HHH syndrome by liquid chromatography tandem mass spectrometry.
Analytical and bioanalytical chemistry 2006;386(7-8):2013-7.
2006: Osama Y Al-Dirbashi; Nafiz Oncu Can; Minnie Jacob; Khalid Al-Qahtani; Mohamed S Rashed
UPLC-MS/MS determination of doxazosine in human plasma.
Analytical and bioanalytical chemistry 2006;385(8):1439-43.
2006: Osama Alsmadi; Fadi Alkayal; Moeenaldeen Al-Sayed; Mohamed S Rashed; Faiqa Imtiaz; Brian F Meyer
LCGreen I-based real-time PCR assays for detecting common ASL and HMGCL variants.
Clinical chemistry 2006;52(7):1439-40.
2006: Ali N Al Odaib; Mohamed S Rashed; Theodore Page; William L Nyhan; Pinar T Ozand
3-Methylcrotonyl-CoA carboxylase deficiency. A long-term outcome.
Saudi medical journal 2006;27(5):732-3.
2006: Osama Y Al-Dirbashi; Nafiz Oncu Can; Ali N Al Odaib; Minnie Jacob; Mohamed S Rashed
Rapid liquid chromatography-tandem mass spectrometry method for quantification of ziprasidone in human plasma.
Biomedical chromatography : BMC 2006;20(4):365-8.
2006: Osama Y Al-Dirbashi; Minnie Jacob; Lujane Y Al-Ahaidib; Khalid Al-Qahtani; Zuhair Rahbeeni; M Al-Owain; Mohamed S Rashed
Quantification of succinylacetone in urine of hepatorenal tyrosinemia patients by HPLC with fluorescence detection.
Clinica chimica acta; international journal of clinical chemistry 2006;365(1-2):243-8.
2006: Osama Y Al-Dirbashi; Mohamed S Rashed; Herman J Ten Brink; Cornelis Jakobs; Najlaa Filimban; Lujane Y Al-Ahaidib; Minnie Jacob; Moeen M Al-Sayed; Zuhair N Al-Hassnan; Eissa Faqeih
Determination of succinylacetone in dried blood spots and liquid urine as a dansylhydrazone by liquid chromatography tandem mass spectrometry.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 2006;831(1-2):274-80.
2006: Moeenaldeen Al-Sayed; Faiqa Imtiaz; Osama Alsmadi; Mohamed S Rashed; Brian F Meyer
Mutations underlying 3-hydroxy-3-methylglutaryl CoA lyase deficiency in the Saudi population.
BMC medical genetics 2006;7():86.
2006: Osama Y Al-Dirbashi; Minnie Jacob; Zuhair N Al-Hassnan; Reem W Chabayta; Fahad El-Badaoui; Mohamed S Rashed
Determination of methylmalonic acid in urine by HPLC with intramolecular excimer-forming fluorescence derivatization.
Biomedical chromatography : BMC 2006;20(1):54-60.
2005: Osama Y Al-Dirbashi; Minnie Jacob; Mohammed Al-Amoudi; Khalid Al-Kahtani; Ali N Al Odaib; Fahad El-Badaoui; Mohamed S Rashed
Quantification of glutaric and 3-hydroxyglutaric acids in urine of glutaric acidemia type I patients by HPLC with intramolecular excimer-forming fluorescence derivatization.
Clinica chimica acta; international journal of clinical chemistry 2005;359(1-2):179-88.
2005: Mohamed Z Seidahmed; E A Alyamani; Mohamed S Rashed; Amal A A Saadallah; OB Abdelbasit; Mohamed M Shaheed; A Rasheed; F A Hamid; M A Sabry
Total truncation of the molybdopterin/dimerization domains of SUOX protein in an Arab family with isolated sulfite oxidase deficiency.
American journal of medical genetics. Part A 2005;136(2):205-9.
2005: Mohamed S Rashed; Lujane Y Al-Ahaidib; Osama Y Al-Dirbashi; Mohammed Al-Amoudi; Moeen M A Al-Sayed; Zuhair Rahbeeni; Zuhair N Al-Hassnan; Abeer Al-Dbaas; Mohamed Al-Owain; Michelle Ni Luanaigh
Tandem mass spectrometric assay of succinylacetone in urine for the diagnosis of hepatorenal tyrosinemia.
Analytical biochemistry 2005;339(2):310-7.
2005: Mohamed S Rashed; Amal A A Saadallah; Zuhair Rahbeeni; Wafaa Eyaid; Mohamed Z Seidahmed; Saad Al-Shahwan; Mustafa A Salih; Mohammad E Osman; Mohammed Al-Amoudi; Lujane Y Al-Ahaidib; Minnie Jacob
Determination of urinary S-sulphocysteine, xanthine and hypoxanthine by liquid chromatography-electrospray tandem mass spectrometry.
Biomedical chromatography : BMC 2005;19(3):223-30.
2005: Moeenaldeen Al-Sayed; Samaher AlAhmed; Osama Alsmadi; H Khalil; Mohamed S Rashed; Faiqa Imtiaz; Brian F Meyer
Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria.
Journal of inherited metabolic disease 2005;28(6):877-83.
2005: Osama Y Al-Dirbashi; Minnie Jacob; Zuhair N Al-Hassnan; Fahad El-Badaoui; Mohamed S Rashed
Diagnosis of methylmalonic acidemia from dried blood spots by HPLC and intramolecular-excimer fluorescence derivatization.
Clinical chemistry 2005;51(1):235-7.
2003: Mohamed S Rashed; Minnie Jacob; Mohammed Al-Amoudi; Zuhair Rahbeeni; Moeenaldeen Al-Sayed; Lujane Y Al-Ahaidib; Amal A A Saadallah; Sharon Legaspi
Rapid determination of orotic acid in urine by liquid chromatography-electrospray tandem mass spectrometry.
Clinical chemistry 2003;49(3):499-501.
2003: Moeenaldeen Al-Sayed; Ali M Al-Asmari; Mohamed S Rashed
Goldenhar syndrome and hereditary tyrosinemia type 1.
Neurosciences (Riyadh, Saudi Arabia) 2003;8(1):55-9.
2002: Moeenaldeen Al-Sayed; Ali M Asmari; Mohamed S Rashed
Goldenhar syndrome and hereditary tyrosinemia type 1.
Saudi medical journal 2002;23(12):1527-31.
2002: Zuhair Rahbeeni; Frédéric M Vaz; Khalid Al-Hussein; MP Bucknall; Jos P N Ruiter; R J Wanders; Mohamed S Rashed
Identification of two novel mutations in OCTN2 from two Saudi patients with systemic carnitine deficiency.
Journal of inherited metabolic disease 2002;25(5):363-9.
2002: Mohamed S Rashed; Nafiz Oncu Can; Mohamed AlAmoudi; Minnie Jakob; Lujaine Y Al-Ahaideb; ABBAS ALABBAD; Suhail Shabib; Emtethal Al-Jishi
Chiral liquid chromatography tandem mass spectrometry in the determination of the configuration of glyceric acid in urine of patients with D-glyceric and L-glyceric acidurias.
Biomedical chromatography : BMC 2002;16(3):191-8.
2001: Mohamed S Rashed; Lujane Y Al-Ahaidib; Nafiz Oncu Can; Mohammed Al-Amoudi; Minnie Jacob
Determination of L-pipecolic acid in plasma using chiral liquid chromatography-electrospray tandem mass spectrometry.
Clinical chemistry 2001;47(12):2124-30.
2001: Mohamed S Rashed
Clinical applications of tandem mass spectrometry: ten years of diagnosis and screening for inherited metabolic diseases.
Journal of chromatography. B, Biomedical sciences and applications 2001;758(1):27-48.
2000: Mohamed S Rashed; Mohamed AlAmoudi; Nafiz Oncu Can
Chiral liquid chromatography tandem mass spectrometry in the determination of the configuration of 2-hydroxyglutaric acid in urine.
Biomedical chromatography : BMC 2000;14(5):317-20.
2000: Mazen Al-Essa; Mohamed S Rashed; Siema M Bakheet; Zoltan Patay; Pinar T Ozand
Glutaric aciduria type II: observations in seven patients with neonatal- and late-onset disease.
Journal of perinatology : official journal of the California Perinatal Association 2000;20(2):120-8.
1999: Mazen Al-Essa; Mohamed S Rashed; Pinar T Ozand
Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic response.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-ṣiḥḥīyah li-sharq al-mutawassiṭ 1999;5(6):1204-7.
1999: Mazen Al-Essa; Mohamed S Rashed; Pinar T Ozand
Classic homocystinuria: clinical, biochemical and radiological observations, and therapeutic outcome of 24 Saudi patients.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-ṣiḥḥīyah li-sharq al-mutawassiṭ 1999;5(6):1196-203.
1999: Mazen Al-Essa; A Al Amir; Mohamed S Rashed; Emtethal Al-Jishi; A Abutaleb; K Mobaireek; Y S Shin; Pinar T Ozand
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography of the brain, MR spectroscopy, and therapeutic attempts in methylenetetrahydrofolate reductase deficiency.
Brain & development 1999;21(5):345-9.
1999: Emtethal Al-Jishi; Brian F Meyer; Mohamed S Rashed; Mazen Al-Essa; Mohamed Al-Hamed; Nadia A Sakati; Sami A Sanjad; Pinar T Ozand; Marios Kambouris
Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.
Clinical genetics 1999;55(6):444-9.
1999: Mohamed S Rashed; Zuhair Rahbeeni; Pinar T Ozand
Application of electrospray tandem mass spectrometry to neonatal screening.
Seminars in perinatology 1999;23(2):183-93.
1999: Mazen Al-Essa; Gursev S Dhaunsi; Mohamed S Rashed; Pinar T Ozand; Zuhair Rahbeeni
Zellweger syndrome in Saudi Arabia and its distinct features.
Clinical pediatrics 1999;38(2):77-86.
1999: Mohamed S Rashed; Zuhair Rahbeeni; Pinar T Ozand
Screening blood spots for argininosuccinase deficiency by electrospray tandem mass spectrometry.
The Southeast Asian journal of tropical medicine and public health 1999;30 Suppl 2():170-3.
1998: Mazen Al-Essa; Zuhair Rahbeeni; S Jumaah; S Joshi; Emtethal Al-Jishi; Mohamed S Rashed; Mohammed Al-Amoudi; Pinar T Ozand
Infectious complications of propionic acidemia in Saudia Arabia.
Clinical genetics 1998;54(1):90-4.
1998: Mazen Al-Essa; Mohamed S Rashed; Pinar T Ozand
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency in a boy with VATER association.
Journal of inherited metabolic disease 1998;21(4):443-4.
1998: Mazen Al-Essa; Mohamed S Rashed; Pinar T Ozand
Saudi experience with classic homocystinuria.
Annals of Saudi medicine 1998;18(3):230-3.
1998: Mazen Al-Essa; Nadia A Sakati; Omar Dabbagh; S Joshi; Emtethal Al-Jishi; Mohamed S Rashed; JE Powe; Pinar T Ozand
Inborn error of vitamin B12 metabolism: a treatable cause of childhood dementia/paralysis.
Journal of child neurology 1998;13(5):239-43.
1998: S Soufi; Mohamed S Rashed; Mazen Al-Essa; MP Bucknall; A Refi; F Badaghesh; H S Habib; Pinar T Ozand
Glutaric acidemia type 1: First Saudi patient diagnosed by tandem mass spectrometry-based neonatal screening.
Annals of Saudi medicine 1998;18(2):160-3.
1998: Mazen Al-Essa; Mohamed S Rashed; Pinar T Ozand
Tyrosinemia type II: Report of the first four cases in Saudi Arabia.
Annals of Saudi medicine 1998;18(5):466-8.
1998: Mazen Al-Essa; LA al-Shamsan; Mohamed S Rashed; Pinar T Ozand
Alkaptonuria: Case report and review of the literature.
Annals of Saudi medicine 1998;18(5):442-4.
1997: Mohamed S Rashed; MP Bucknall; D Little; A Awad; Minnie Jacob; Mohamed AlAmoudi; M Alwattar; Pinar T Ozand
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 profiles.
Clinical chemistry 1997;43(7):1129-41.
1996: Najya A Attia; Nadia A Sakati; Abdullah A Al-Ashwal; R al Saif; Mohamed S Rashed; Pinar T Ozand
Isovaleric acidemia appearing as diabetic ketoacidosis.
Journal of inherited metabolic disease 1996;19(1):85-6.
1995: Mohamed S Rashed; Pinar T Ozand; M P Bucknall; D Little
Diagnosis of inborn errors of metabolism from blood spots by acylcarnitines and amino acids profiling using automated electrospray tandem mass spectrometry.
Pediatric research 1995;38(3):324-31.
1995: Mohamed S Rashed; Pinar T Ozand; M J Bennett; J J Barnard; D R Govindaraju; P Rinaldo
Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bile.
Clinical chemistry 1995;41(8 Pt 1):1109-14.
1994: H G Worthen; Abdullah A Al-Ashwal; Pinar T Ozand; S Garawi; Zuhair Rahbeeni; A al Odaib; S B Subramanyam; Mohamed S Rashed
Comparative frequency and severity of hypoglycemia in selected organic acidemias, branched chain amino acidemia, and disorders of fructose metabolism.
Brain & development 1994;16 Suppl():81-5.
1994: Zuhair Rahbeeni; Pinar T Ozand; Mohamed S Rashed; G G Gascon; M al Nasser; A al Odaib; M Amoudi; M Nester; S al Garawi; J Brismar
4-Hydroxybutyric aciduria.
Brain & development 1994;16 Suppl():64-71.
1994: Pinar T Ozand; Mohamed S Rashed; G G Gascon; N G Youssef; HA Harfi; Zuhair Rahbeeni; S al Garawi; A al Aqeel
Unusual presentations of propionic acidemia.
Brain & development 1994;16 Suppl():46-57.
1994: Pinar T Ozand; Mohamed S Rashed; G G Gascon; A al Odaib; A Shums; M Nester; J Brismar
3-Ketothiolase deficiency: a review and four new patients with neurologic symptoms.
Brain & development 1994;16 Suppl():38-45.
1994: A al Aqeel; Mohamed S Rashed; Pinar T Ozand; G G Gascon; Zuhair Rahbeeni; S al Garawi; A al Odaib; J Brismar
A new patient with alpha-ketoglutaric aciduria and progressive extrapyramidal tract disease.
Brain & development 1994;16 Suppl():33-7.
1994: A al Aqeel; Mohamed S Rashed; Pinar T Ozand; J Brismar; G G Gascon; A al Odaib; Omar Dabbagh
3-Methylglutaconic aciduria: ten new cases with a possible new phenotype.
Brain & development 1994;16 Suppl():23-32.
1994: Pinar T Ozand; Mohamed S Rashed; D S Millington; Nadia A Sakati; SELWA AL-HAZZAA; Zuhair Rahbeeni; A al Odaib; N Youssef; A Mazrou; G G Gascon
Ethylmalonic aciduria: an organic acidemia with CNS involvement and vasculopathy.
Brain & development 1994;16 Suppl():12-22.
1994: Mohamed S Rashed; Pinar T Ozand; A al Aqeel; G G Gascon
Experience of King Faisal Specialist Hospital and Research Center with Saudi organic acid disorders.
Brain & development 1994;16 Suppl():1-6.