Al-Ali A - Search Results

1

Intronic Polymorphisms in the CDKN2B-AS1 Gene Are Strongly Associated with the Risk of Myocardial Infarction and Coronary Artery Disease in the Saudi Population.

AbdulAzeez S, Al-Nafie AN, Al-Shehri A, Borgio JF, Baranova EV, Al-Madan MS, Al-Ali RA, Al-Muhanna F, Al-Ali A, Al-Mansori M, Ibrahim MF, Asselbergs FW, Keating B, Koeleman BP, Al-Ali AK. AbdulAzeez S, et al. Int J Mol Sci. 2016 Mar 17;17(3):395. doi: 10.3390/ijms17030395. Int J Mol Sci. 2016. PMID: 26999117 Free PMC article.

2

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Eastern Province of Saudi Arabia.

Al-Ali AK, Al-Mustafa ZH, Al-Madan M, Qaw F, Al-Ateeq S. Al-Ali AK, et al. Clin Chem Lab Med. 2002 Aug;40(8):814-6. doi: 10.1515/CCLM.2002.141. Clin Chem Lab Med. 2002. PMID: 12392311

3

Molecular bases of beta-thalassemia in the Eastern Province of Saudi Arabia.

Al-Ali AK, Al-Ateeq S, Imamwerdi BW, Al-Sowayan S, Al-Madan M, Al-Muhanna F, Bashaweri L, Qaw F. Al-Ali AK, et al. J Biomed Biotechnol. 2005;2005(4):322-5. doi: 10.1155/JBB.2005.322. J Biomed Biotechnol. 2005. PMID: 16489266 Free PMC article.

4

Vitamin D deficiency and rickets in the Eastern Province of Saudi Arabia.

Al-Mustafa ZH, Al-Madan M, Al-Majid HJ, Al-Muslem S, Al-Ateeq S, Al-Ali AK. Al-Mustafa ZH, et al. Ann Trop Paediatr. 2007 Mar;27(1):63-7. doi: 10.1179/146532807X170529. Ann Trop Paediatr. 2007. PMID: 17469734

5

Polymorphism in methylenetetrahydrofolate reductase, plasminogen activator inhibitor-1, and apolipoprotein E in hemodialysis patients.

Al-Muhanna F, Al-Mueilo S, Al-Ali A, Larbi E, Rubaish A, Abdulmohsen MF, Al-Zahrani A, Al-Ateeq S. Al-Muhanna F, et al. Saudi J Kidney Dis Transpl. 2008 Nov;19(6):937-41. Saudi J Kidney Dis Transpl. 2008. PMID: 18974580

6

Spectrum of α-thalassemia mutations in transfusion-dependent β-thalassemia patients from the Eastern Province of Saudi Arabia.

Akhtar MS, Qaw F, Borgio JF, Albuali W, Suliman A, Nasserullah Z, Al-Jarrash S, Al-Ali A. Akhtar MS, et al. Hemoglobin. 2013;37(1):65-73. doi: 10.3109/03630269.2012.753510. Hemoglobin. 2013. PMID: 23297837

7

Increased Prevalence of Glycoprotein IIb/IIIa Leu 33 Pro Polymorphism in End Stage Renal Disease Patients on Hemodialysis.

Al-Ali A, Al-Muhanna F, Al-Mueilo S, Larbi E, Al-Sultan A, Rubaish A, Al-Ateeq S, Al-Zaharani A. Al-Ali A, et al. Int J Biomed Sci. 2008 Sep;4(3):175-8. Int J Biomed Sci. 2008. PMID: 23675086 Free PMC article.

8

A novel HBA2 gene conversion in cis or trans: "α12 allele" in a Saudi population.

Borgio JF, AbdulAzeez S, Al-Nafie AN, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Muhanna F, Steinberg MH, Al-Ali AK. Borgio JF, et al. Blood Cells Mol Dis. 2014 Dec;53(4):199-203. doi: 10.1016/j.bcmd.2014.07.001. Epub 2014 Jul 25. Blood Cells Mol Dis. 2014. PMID: 25065854

9

BCL11A enhancer haplotypes and fetal hemoglobin in sickle cell anemia.

Sebastiani P, Farrell JJ, Alsultan A, Wang S, Edward HL, Shappell H, Bae H, Milton JN, Baldwin CT, Al-Rubaish AM, Naserullah Z, Al-Muhanna F, Alsuliman A, Patra PK, Farrer LA, Ngo D, Vathipadiekal V, Chui DH, Al-Ali AK, Steinberg MH. Sebastiani P, et al. Blood Cells Mol Dis. 2015 Mar;54(3):224-30. doi: 10.1016/j.bcmd.2015.01.001. Epub 2015 Jan 30. Blood Cells Mol Dis. 2015. PMID: 25703683 Free PMC article.

10

Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients.

Al-Nafie AN, Borgio JF, AbdulAzeez S, Al-Suliman AM, Qaw FS, Naserullah ZA, Al-Jarrash S, Al-Madan MS, Al-Ali RA, AlKhalifah MA, Al-Muhanna F, Steinberg MH, Al-Ali AK. Al-Nafie AN, et al. Blood Cells Mol Dis. 2015 Jun;55(1):27-9. doi: 10.1016/j.bcmd.2015.03.008. Epub 2015 Mar 30. Blood Cells Mol Dis. 2015. PMID: 25976463

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