Rashed MS - Search Results

1

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with stroke-like imaging presentation: clinical, biochemical and molecular analysis.

Al-Hassnan ZN, Rashed MS, Al-Dirbashi OY, Patay Z, Rahbeeni Z, Abu-Amero KK. Al-Hassnan ZN, et al. Among authors: rashed ms. J Neurol Sci. 2008 Jan 15;264(1-2):187-94. doi: 10.1016/j.jns.2007.08.003. Epub 2007 Sep 7. J Neurol Sci. 2008. PMID: 17825324

2

Determination of homocitrulline in urine of patients with HHH syndrome by liquid chromatography tandem mass spectrometry.

Al-Dirbashi OY, Al-Hassnan ZN, Rashed MS. Al-Dirbashi OY, et al. Among authors: rashed ms. Anal Bioanal Chem. 2006 Dec;386(7-8):2013-7. doi: 10.1007/s00216-006-0831-5. Epub 2006 Oct 20. Anal Bioanal Chem. 2006. PMID: 17053917

3

Medium-chain acyl-CoA dehydrogenase deficiency in Saudi Arabia: incidence, genotype, and preventive implications.

Al-Hassnan ZN, Imtiaz F, Al-Amoudi M, Rahbeeni Z, Al-Sayed M, Al-Owain M, Al-Zaidan H, Al-Odaib A, Rashed MS. Al-Hassnan ZN, et al. Among authors: rashed ms. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S263-7. doi: 10.1007/s10545-010-9143-1. Epub 2010 Jun 22. J Inherit Metab Dis. 2010. PMID: 20567907

4

Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin.

Imtiaz F, Rashed MS, Al-Mubarak B, Allam R, El-Karaksy H, Al-Hassnan Z, Al-Owain M, Al-Zaidan H, Rahbeeni Z, Qari A, Meyer BF, Al-Sayed M. Imtiaz F, et al. Among authors: rashed ms. Mol Genet Metab. 2011 Dec;104(4):688-90. doi: 10.1016/j.ymgme.2011.06.019. Epub 2011 Jun 30. Mol Genet Metab. 2011. PMID: 21764616

5

Preimplantation genetic diagnosis in isolated sulfite oxidase deficiency.

Salih MA, Bosley TM, Alorainy IA, Sabry MA, Rashed MS, Al-Yamani EA, El-Akoum S, Mohamed SH, Abu-Amero KK, Hellani AM. Salih MA, et al. Among authors: rashed ms. Can J Neurol Sci. 2013 Jan;40(1):109-12. doi: 10.1017/s0317167100013081. Can J Neurol Sci. 2013. PMID: 23250141 No abstract available.

6

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.

Al-Dirbashi OY, Abu-Amero KK, Alswaid AF, Hoffmann GF, Al-Qahtani K, Rashed MS. Al-Dirbashi OY, et al. Among authors: rashed ms. J Inherit Metab Dis. 2007 Aug;30(4):611. doi: 10.1007/s10545-007-0670-3. Epub 2007 Aug 15. J Inherit Metab Dis. 2007. PMID: 17701443

7

Expanded Newborn Screening Program in Saudi Arabia: Incidence of screened disorders.

Alfadhel M, Al Othaim A, Al Saif S, Al Mutairi F, Alsayed M, Rahbeeni Z, Alzaidan H, Alowain M, Al-Hassnan Z, Saeedi M, Aljohery S, Alasmari A, Faqeih E, Alwakeel M, AlMashary M, Almohameed S, Alzahrani M, Migdad A, Al-Dirbashi OY, Rashed M, Alamoudi M, Jacob M, Alahaidib L, El-Badaoui F, Saadallah A, Alsulaiman A, Eyaid W, Al-Odaib A. Alfadhel M, et al. J Paediatr Child Health. 2017 Jun;53(6):585-591. doi: 10.1111/jpc.13469. Epub 2017 Mar 24. J Paediatr Child Health. 2017. PMID: 28337809

8

Diagnosis of methylmalonic acidemia from dried blood spots by HPLC and intramolecular-excimer fluorescence derivatization.

Al-Dirbashi OY, Jacob M, Al-Hassnan Z, El-Badaoui F, Rashed MS. Al-Dirbashi OY, et al. Among authors: rashed ms. Clin Chem. 2005 Jan;51(1):235-7. doi: 10.1373/clinchem.2004.040022. Epub 2004 Oct 28. Clin Chem. 2005. PMID: 15514093 No abstract available.

9

Tandem mass spectrometric assay of succinylacetone in urine for the diagnosis of hepatorenal tyrosinemia.

Rashed MS, Al-Ahaidib LY, Al-Dirbashi OY, Al Amoudi M, Al-Sayed MM, Rahbeeni Z, Al-Hassnan Z, Al-Dbaas A, Al-Owain M, Ni Luanaigh M. Rashed MS, et al. Anal Biochem. 2005 Apr 15;339(2):310-7. doi: 10.1016/j.ab.2005.01.014. Anal Biochem. 2005. PMID: 15797572

10

Determination of methylmalonic acid in urine by HPLC with intramolecular excimer-forming fluorescence derivatization.

Al-Dirbashi OY, Jacob M, Al-Hassnan Z, Chabayta RW, El-Badaoui F, Rashed MS. Al-Dirbashi OY, et al. Among authors: rashed ms. Biomed Chromatogr. 2006 Jan;20(1):54-60. doi: 10.1002/bmc.527. Biomed Chromatogr. 2006. PMID: 15966058

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