Bitar F - Search Results

1

Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysms.

Abu-Safieh L, Abboud EB, Alkuraya H, Shamseldin H, Al-Enzi S, Al-Abdi L, Hashem M, Colak D, Jarallah A, Ahmad H, Bobis S, Nemer G, Bitar F, Alkuraya FS. Abu-Safieh L, et al. Among authors: bitar f. Am J Hum Genet. 2011 Aug 12;89(2):313-9. doi: 10.1016/j.ajhg.2011.07.010. Am J Hum Genet. 2011. PMID: 21835307 Free PMC article.

2

COVID-19 in Cyanotic Congenital Heart Disease.

Ammar LA, Nassar JE, Bitar F, Arabi M. Ammar LA, et al. Among authors: bitar f. Can J Infect Dis Med Microbiol. 2023 Apr 18;2023:5561159. doi: 10.1155/2023/5561159. eCollection 2023. Can J Infect Dis Med Microbiol. 2023. PMID: 37114013 Free PMC article. Review.

3

Pulmonary artery debanding in the cath lab: Lessons learned!

Zareef R, Hassan SA, Younis N, Tannoury T, Rassi IE, Bitar F, Arabi M. Zareef R, et al. Among authors: bitar f. Front Cardiovasc Med. 2022 Dec 15;9:950123. doi: 10.3389/fcvm.2022.950123. eCollection 2022. Front Cardiovasc Med. 2022. PMID: 36588562 Free PMC article.

4

Low molecular weight heparin in COVID-19: benefits and concerns.

Makarem A, Zareef R, Abourjeili J, Nassar JE, Bitar F, Arabi M. Makarem A, et al. Among authors: bitar f. Front Pharmacol. 2023 Apr 27;14:1159363. doi: 10.3389/fphar.2023.1159363. eCollection 2023. Front Pharmacol. 2023. PMID: 37180701 Free PMC article. Review.

5

Combined tricuspid atresia- AV septal defect-a rare congenital cardiac abnormality.

Bassam K, Farhat A, El-Rassi I, Bitar F, Arabi M. Bassam K, et al. Among authors: bitar f. Echocardiography. 2023 Oct;40(10):1094-1098. doi: 10.1111/echo.15684. Epub 2023 Aug 29. Echocardiography. 2023. PMID: 37641570

6

Transcatheter occlusion of a hepatic vein-to-left atrium fistula: Should we close venovenous collateral vessels following Fontan operation?

El-Khouri M, Arabi M, El Rassi I, Bulbul Z, Sawaya F, Bitar F. El-Khouri M, et al. Among authors: bitar f. Ann Pediatr Cardiol. 2022 Jul-Aug;15(4):415-418. doi: 10.4103/apc.apc_193_21. Epub 2023 Jan 6. Ann Pediatr Cardiol. 2022. PMID: 36935823 Free PMC article.

7

Tamponade and massive pleural effusions secondary to peripherally inserted central catheter in neonates-A complication to be aware of.

Zareef R, Anka M, Hatab T, El Rassi I, Yunis K, Bitar F, Arabi M. Zareef R, et al. Among authors: bitar f. Front Cardiovasc Med. 2023 Feb 17;10:1092814. doi: 10.3389/fcvm.2023.1092814. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 36873398 Free PMC article.

8

A novel mutation in the GATA4 gene in patients with Tetralogy of Fallot.

Nemer G, Fadlalah F, Usta J, Nemer M, Dbaibo G, Obeid M, Bitar F. Nemer G, et al. Among authors: bitar f. Hum Mutat. 2006 Mar;27(3):293-4. doi: 10.1002/humu.9410. Hum Mutat. 2006. PMID: 16470721

9

Exclusive cardiac dysfunction in familial primary carnitine deficiency cases: a genotype-phenotype correlation.

Yamak A, Bitar F, Karam P, Nemer G. Yamak A, et al. Among authors: bitar f. Clin Genet. 2007 Jul;72(1):59-62. doi: 10.1111/j.1399-0004.2007.00814.x. Clin Genet. 2007. PMID: 17594400 No abstract available.

10

Absence of NOTCH2 and Hey2 mutations in a familial Alagille syndrome case with a novel frameshift mutation in JAG1.

El-Rassy I, Bou-Abdallah J, Al-Ghadban S, Bitar F, Nemer G. El-Rassy I, et al. Among authors: bitar f. Am J Med Genet A. 2008 Apr 1;146A(7):937-9. doi: 10.1002/ajmg.a.32225. Am J Med Genet A. 2008. PMID: 18266235 No abstract available.

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