Al-Nabhani M - Search Results

1

Variability of non-lethal Fowler syndrome phenotype associated with FLVCR2 variants.

Al-Murshedi F, Mirza H, Al-Saegh A, Al-Nabhani M, Al-Shabibi S, Baawain S, Al-Futaisi A, Al-Shehhi W, Al-Maawali A. Al-Murshedi F, et al. Among authors: al nabhani m. Clin Genet. 2020 Nov;98(5):520-521. doi: 10.1111/cge.13838. Epub 2020 Sep 9. Clin Genet. 2020. PMID: 32901920 No abstract available.

2

Homozygosity for FARSB mutation leads to Phe-tRNA synthetase-related disease of growth restriction, brain calcification, and interstitial lung disease.

Zadjali F, Al-Yahyaee A, Al-Nabhani M, Al-Mubaihsi S, Gujjar A, Raniga S, Al-Maawali A. Zadjali F, et al. Among authors: al nabhani m. Hum Mutat. 2018 Oct;39(10):1355-1359. doi: 10.1002/humu.23595. Epub 2018 Jul 30. Hum Mutat. 2018. PMID: 30014610

3

Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits.

Al-Nabhani M, Al-Rashdi S, Al-Murshedi F, Al-Kindi A, Al-Thihli K, Al-Saegh A, Al-Futaisi A, Al-Mamari W, Zadjali F, Al-Maawali A. Al-Nabhani M, et al. Clin Genet. 2018 Dec;94(6):495-501. doi: 10.1111/cge.13438. Epub 2018 Sep 12. Clin Genet. 2018. PMID: 30125339

4

Phenotypic spectrum of ALPK3-related cardiomyopathy.

Al Senaidi K, Joshi N, Al-Nabhani M, Al-Kasbi G, Al Farqani A, Al-Thihli K, Al-Maawali A. Al Senaidi K, et al. Among authors: al nabhani m. Am J Med Genet A. 2019 Jul;179(7):1235-1240. doi: 10.1002/ajmg.a.61176. Epub 2019 May 10. Am J Med Genet A. 2019. PMID: 31074094

5

A Novel Splice-Site Variant in SLC12A6 Causes Andermann Syndrome without Agenesis of the Corpus Callosum.

Al Shibli N, Al-Maawali A, Elmanzalawy A, Al-Nabhani M, Koul R, Gabr A, Al Murshedi F. Al Shibli N, et al. Among authors: al nabhani m. J Pediatr Genet. 2020 Dec;9(4):293-295. doi: 10.1055/s-0039-1700975. Epub 2020 Jan 6. J Pediatr Genet. 2020. PMID: 32765936 Free PMC article.

6

Combined polymorphism analysis of glutathione S-transferase M1/G1 and interleukin-1B (IL-1B)/interleukin 1-receptor antagonist (IL-1RN) and gastric cancer risk in an Omani Arab Population.

Al-Moundhri MS, Alkindy M, Al-Nabhani M, Al-Bahrani B, Burney IA, Al-Habsi H, Ganguly SS, Tanira M. Al-Moundhri MS, et al. J Clin Gastroenterol. 2009 Feb;43(2):152-6. doi: 10.1097/MCG.0b013e31815853fa. J Clin Gastroenterol. 2009. PMID: 18779738

7

Association of E-cadherin (CDH1) gene polymorphisms and gastric cancer risk.

Al-Moundhri MS, Al-Khanbashi M, Al-Kindi M, Al-Nabhani M, Burney IA, Al-Farsi A, Al-Bahrani B. Al-Moundhri MS, et al. World J Gastroenterol. 2010 Jul 21;16(27):3432-6. doi: 10.3748/wjg.v16.i27.3432. World J Gastroenterol. 2010. PMID: 20632448 Free PMC article.

8

Gastric cancer risk predisposition and prognostic significance of vascular endothelial growth factor (VEGF) gene polymorphisms--a case-control study in an Omani population.

Al-Moundhri MS, Al-Nabhani M, Burney IA, Al-Farsi AA, Al-Bahrani B. Al-Moundhri MS, et al. Mol Carcinog. 2009 Dec;48(12):1170-6. doi: 10.1002/mc.20572. Mol Carcinog. 2009. PMID: 19676106

9

NAT2 polymorphism in Omani gastric cancer patients-risk predisposition and clinicopathological associations.

Al-Moundhri MS, Al-Kindi M, Al-Nabhani M, Al-Bahrani B, Burney IA, Al-Madhani A, Ganguly SS, Tanira M. Al-Moundhri MS, et al. World J Gastroenterol. 2007 May 21;13(19):2697-702. doi: 10.3748/wjg.v13.i19.2697. World J Gastroenterol. 2007. PMID: 17569138 Free PMC article.

10

The prognostic significance of p53, p27 kip1, p21 waf1, HER-2/neu, and Ki67 proteins expression in gastric cancer: a clinicopathological and immunohistochemical study of 121 Arab patients.

Al-Moundhri MS, Nirmala V, Al-Hadabi I, Al-Mawaly K, Burney I, Al-Nabhani M, Thomas V, Ganguly SS, Grant C. Al-Moundhri MS, et al. J Surg Oncol. 2005 Sep 15;91(4):243-52. doi: 10.1002/jso.20324. J Surg Oncol. 2005. PMID: 16121348

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