Rashed M - Search Results

1

Al-Owain M, Imtiaz F, Shuaib T, Edrees A, Al-Amoudi M, Sakati N, Al-Hassnan Z, Bamashmous H, Rahbeeni Z, Al-Ameer S, Faqeih E, Meyer B, Al-Hashem A, Garout W, Al-Odaib A, Rashed M, Al-Aama JY. Al-Owain M, et al. Among authors: rashed m. Clin Genet. 2012 Aug;82(2):165-72. doi: 10.1111/j.1399-0004.2011.01742.x. Epub 2011 Jul 18. Clin Genet. 2012. PMID: 21696385

2

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

3

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

4

Infectious complications of propionic acidemia in Saudia Arabia.

Al Essa M, Rahbeeni Z, Jumaah S, Joshi S, Al Jishi E, Rashed MS, Al Amoudi M, Ozand PT. Al Essa M, et al. Among authors: rashed ms. Clin Genet. 1998 Jul;54(1):90-4. doi: 10.1111/j.1399-0004.1998.tb03702.x. Clin Genet. 1998. PMID: 9727749

5

Clinical, biochemical, and molecular characterization of patients with glutathione synthetase deficiency.

Al-Jishi E, Meyer BF, Rashed MS, Al-Essa M, Al-Hamed MH, Sakati N, Sanjad S, Ozand PT, Kambouris M. Al-Jishi E, et al. Among authors: rashed ms. Clin Genet. 1999 Jun;55(6):444-9. doi: 10.1034/j.1399-0004.1999.550608.x. Clin Genet. 1999. PMID: 10450861

6

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. 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

7

Zellweger syndrome in Saudi Arabia and its distinct features.

al-Essa M, Dhaunsi GS, Rashed M, Ozand PT, Rahbeeni Z. al-Essa M, et al. Among authors: rashed m. Clin Pediatr (Phila). 1999 Feb;38(2):77-86. doi: 10.1177/000992289903800203. Clin Pediatr (Phila). 1999. PMID: 10047940

8

Identification of a common novel mutation in Saudi patients with argininosuccinic aciduria.

Al-Sayed M, Alahmed S, Alsmadi O, Khalil H, Rashed MS, Imtiaz F, Meyer BF. Al-Sayed M, et al. Among authors: rashed ms. J Inherit Metab Dis. 2005;28(6):877-83. doi: 10.1007/s10545-005-0081-2. J Inherit Metab Dis. 2005. PMID: 16435180

9

The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population.

Imtiaz F, Savilahti E, Sarnesto A, Trabzuni D, Al-Kahtani K, Kagevi I, Rashed MS, Meyer BF, Järvelä I. Imtiaz F, et al. Among authors: rashed ms. J Med Genet. 2007 Oct;44(10):e89. doi: 10.1136/jmg.2007.051631. J Med Genet. 2007. PMID: 17911653 Free PMC article.

10

Glutaric aciduria yype 1: First reported cases in three Saudi patients.

Coates R, Rashed M, Rahbeeni Z, Al-Garawi S, Al-Odaib AN, Sakati N, Gascon G, Worthen H, Ozand PT. Coates R, et al. Among authors: rashed m. Ann Saudi Med. 1994 Jul;14(4):316-21. doi: 10.5144/0256-4947.1994.316. Ann Saudi Med. 1994. PMID: 17586927 Free PMC article.

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