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Page 1
Identification of Gaucher disease mutations found in Saudi Arabia.
Kaya N, Al-Zahrani F, Al-Odaib A, Rahbeeni Z, Al-Hassnan Z, Al-Sharif F, Ozand P, Al-Sayed M. Kaya N, et al. Among authors: rahbeeni z. Blood Cells Mol Dis. 2008 Sep-Oct;41(2):200-1. doi: 10.1016/j.bcmd.2008.05.002. Epub 2008 Jun 30. Blood Cells Mol Dis. 2008. PMID: 18586535 No abstract available.
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: rahbeeni z. Clin Pediatr (Phila). 1999 Feb;38(2):77-86. doi: 10.1177/000992289903800203. Clin Pediatr (Phila). 1999. PMID: 10047940
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: rahbeeni z. 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.
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency.
Faiyaz-Ul-Haque M, Al-Owain M, Al-Dayel F, Al-Hassnan Z, Al-Zaidan H, Rahbeeni Z, Al-Sayed M, Balobaid A, Cluntun A, Toulimat M, Abalkhail H, Peltekova I, Zaidi SH. Faiyaz-Ul-Haque M, et al. Among authors: rahbeeni z. Eur J Pediatr. 2009 Dec;168(12):1467-71. doi: 10.1007/s00431-009-0953-9. Epub 2009 Mar 4. Eur J Pediatr. 2009. PMID: 19259699
Novel mutation in GLRB in a large family with hereditary hyperekplexia.
Al-Owain M, Colak D, Al-Bakheet A, Al-Hashmi N, Shuaib T, Al-Hemidan A, Aldhalaan H, Rahbeeni Z, Al-Sayed M, Al-Younes B, Ozand PT, Kaya N. Al-Owain M, et al. Among authors: rahbeeni z. Clin Genet. 2012 May;81(5):479-84. doi: 10.1111/j.1399-0004.2011.01661.x. Epub 2011 Apr 7. Clin Genet. 2012. PMID: 21391991
91 results