Abu-Amero KK - Search Results

1

Association of mitochondrial haplogroups H and R with keratoconus in Saudi Arabian patients.

Abu-Amero KK, Azad TA, Sultan T, Kalantan H, Kondkar AA, Al-Muammar AM. Abu-Amero KK, et al. Invest Ophthalmol Vis Sci. 2014 May 1;55(5):2827-31. doi: 10.1167/iovs.14-14300. Invest Ophthalmol Vis Sci. 2014. PMID: 24722698

2

Prevalence of the 20210 G-->A prothrombin variant and its association with coronary artery disease in a Middle Eastern Arab population.

Abu-Amero KK, Wyngaard CA, Kambouris M, Dzimiri N. Abu-Amero KK, et al. Arch Pathol Lab Med. 2002 Sep;126(9):1087-90. doi: 10.5858/2002-126-1087-POTGAP. Arch Pathol Lab Med. 2002. PMID: 12204058

3

Lack of association of lipoprotein lipase gene polymorphisms with coronary artery disease in the Saudi Arab population.

Abu-Amero KK, Wyngaard CA, Al-Boudari OM, Kambouris M, Dzimiri N. Abu-Amero KK, et al. Arch Pathol Lab Med. 2003 May;127(5):597-600. doi: 10.5858/2003-127-0597-LOAOLL. Arch Pathol Lab Med. 2003. PMID: 12708905

4

Human genetics information on the Web.

Abu-Amero K. Abu-Amero K. J R Soc Promot Health. 2003 Jun;123(2):102-4. doi: 10.1177/146642400312300214. J R Soc Promot Health. 2003. PMID: 12852194

5

Prevalence and role of methylenetetrahydrofolate reductase 677 C-->T and 1298 A-->C polymorphisms in coronary artery disease in Arabs.

Abu-Amero KK, Wyngaard CA, Dzimiri N. Abu-Amero KK, et al. Arch Pathol Lab Med. 2003 Oct;127(10):1349-52. doi: 10.5858/2003-127-1349-PAROMR. Arch Pathol Lab Med. 2003. PMID: 14521457

6

A new era for preventive genetic programs in the Arabian Peninsula.

Al-Odaib AN, Abu-Amero KK, Ozand PT, Al-Hellani AM. Al-Odaib AN, et al. Saudi Med J. 2003 Nov;24(11):1168-75. Saudi Med J. 2003. PMID: 14647548 Review.

7

Association of the platelet glycoprotein receptor IIIa (PlA1/PlA1) genotype with coronary artery disease in Arabs.

Abu-Amero KK, Wyngaard CA, Dzimiri N. Abu-Amero KK, et al. Blood Coagul Fibrinolysis. 2004 Jan;15(1):77-9. doi: 10.1097/00001721-200401000-00012. Blood Coagul Fibrinolysis. 2004. PMID: 15166947

8

A novel splice site mutation in the WAS gene causes Wiskott-Aldrich syndrome in two siblings of a Saudi family.

Abu-Amero KK, Owaidah TM, Al Jefri A, Al-Ghonaium A, Fawaz IM, Al-Hamed MH. Abu-Amero KK, et al. Blood Coagul Fibrinolysis. 2004 Oct;15(7):599-603. doi: 10.1097/00001721-200410000-00011. Blood Coagul Fibrinolysis. 2004. PMID: 15389128

9

Mitochondrial DNA nucleotide changes in non-arteritic ischemic optic neuropathy.

Bosley TM, Abu-Amero KK, Ozand PT. Bosley TM, et al. Neurology. 2004 Oct 12;63(7):1305-8. doi: 10.1212/01.wnl.0000140696.34117.95. Neurology. 2004. PMID: 15477560

10

High frequency of somatic mitochondrial DNA mutations in human thyroid carcinomas and complex I respiratory defect in thyroid cancer cell lines.

Abu-Amero KK, Alzahrani AS, Zou M, Shi Y. Abu-Amero KK, et al. Oncogene. 2005 Feb 17;24(8):1455-60. doi: 10.1038/sj.onc.1208292. Oncogene. 2005. PMID: 15608681

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