Taher AT - Search Results

1

Compound heterozygosity for factor V and methylenetetrahydrofolate reductase mutations in a patient with Budd-Chiari syndrome.

Otrock ZK, Sharara AI, Mahfouz RA, Taher AT. Otrock ZK, et al. Among authors: taher at. J Gastroenterol Hepatol. 2006 Apr;21(4):782-3. doi: 10.1111/j.1440-1746.2006.04248.x. J Gastroenterol Hepatol. 2006. PMID: 16677174 No abstract available.

2

Budd-Chiari syndrome with underlying homozygous factor V Leiden and heterozygous methylenetetrahydrofolate reductase mutations.

Barada KA, Azar CR, Otrock ZK, Taher AT. Barada KA, et al. Among authors: taher at. J Gastroenterol. 2005 Oct;40(10):1002-3. doi: 10.1007/s00535-005-1664-2. J Gastroenterol. 2005. PMID: 16261441 No abstract available.

3

Budd-Chiari syndrome in a paroxysmal nocturnal hemoglobinuria patient with coexistence of factor II and MTHFR mutations.

Shamseddine AI, Otrock ZK, Mahfouz RA, Makarem JA, Taher AT. Shamseddine AI, et al. Among authors: taher at. J Thromb Haemost. 2005 May;3(5):1111. doi: 10.1111/j.1538-7836.2005.01283.x. J Thromb Haemost. 2005. PMID: 15869626 Free article. No abstract available.

4

JAK2V617F and prothrombin G20210A gene mutations in a patient with Budd-Chiari syndrome and essential thrombocythemia.

Musallam KM, Aoun EG, Mahfouz RA, Khalife M, Taher AT. Musallam KM, et al. Among authors: taher at. Clin Appl Thromb Hemost. 2010 Aug;16(4):472-4. doi: 10.1177/1076029609332110. Epub 2009 Feb 16. Clin Appl Thromb Hemost. 2010. PMID: 19223280 Free article.

5

Massive pulmonary embolism associated with Factor V Leiden, prothrombin, and methylenetetrahydrofolate reductase gene mutations in a young patient on oral contraceptive pills: a case report.

Charafeddine KM, Mahfouz RA, Ibrahim GY, Taher AT, Hoballah JJ, Taha AM. Charafeddine KM, et al. Among authors: taher at. Clin Appl Thromb Hemost. 2010 Oct;16(5):594-8. doi: 10.1177/1076029609334629. Epub 2009 Jun 10. Clin Appl Thromb Hemost. 2010. PMID: 19520679 Free article.

6

The role of liver iron in hepatitis C antiviral treatment.

Musallam KM, Sharara AI, Inati A, Taher AT. Musallam KM, et al. Among authors: taher at. Eur J Gastroenterol Hepatol. 2010 Jun;22(6):769. doi: 10.1097/MEG.0b013e32832e0a56. Eur J Gastroenterol Hepatol. 2010. PMID: 20440118 No abstract available.

7

Treatment of acute hepatitis C in a child with thalassemia major using weight-based peginterferon alpha-2b.

Sharara AI, Aoun E, Koussa S, Inati A, Taher A. Sharara AI, et al. J Gastroenterol Hepatol. 2006 Jul;21(7):1221. doi: 10.1111/j.1440-1746.2006.04174.x. J Gastroenterol Hepatol. 2006. PMID: 16824084 No abstract available.

8

Frequency of triple mutations involving factor V, prothrombin, and methylenetetrahydrofolate reductase genes among patients referred for molecular thrombophilia workup in a tertiary care center in Lebanon.

Hoteit R, Taher A, Nassar R, Otrock Z, Halawi R, Mahfouz RA. Hoteit R, et al. Genet Test Mol Biomarkers. 2012 Mar;16(3):223-5. doi: 10.1089/gtmb.2011.0114. Epub 2011 Oct 24. Genet Test Mol Biomarkers. 2012. PMID: 22023246

9

Acute myocardial infarction in a young man: a consequence of inherited thrombophilia and marijuana smoking.

Taher AT, Mahfouz RA, Otrock ZK, Rebeiz AG, Sawaya JI. Taher AT, et al. Thromb Haemost. 2006 Jun;95(6):1044. doi: 10.1160/TH06-03-0169. Thromb Haemost. 2006. PMID: 16732390 No abstract available.

10

Homozygous methylenetetrahydrofolate reductase C677T mutation in a woman with spinal cord infarction.

Mahfouz RA, Otrock ZK, Kanaan ZM, Sawaya RA, Taher AT. Mahfouz RA, et al. Among authors: taher at. Eur J Neurol. 2006 Sep;13(9):e4. doi: 10.1111/j.1468-1331.2006.01346.x. Eur J Neurol. 2006. PMID: 16930349 No abstract available.

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