Daher R - Search Results

1

CFTR mutational screening by next-generation sequencing reveals novel variants and a high carrier rate in a Middle Eastern population.

Farra C, Awwad J, Hamadeh L, Khoueiry P, Halawi Z, Yazbeck N, Daher R, Souaid M, Hamdar L, Yammine T, Yunis K. Farra C, et al. Among authors: daher r. Ann Hum Genet. 2022 Mar;86(2):80-86. doi: 10.1111/ahg.12450. Epub 2021 Dec 9. Ann Hum Genet. 2022. PMID: 34888852

2

Incidence of alpha-globin gene defect in the Lebanese population: a pilot study.

Farra C, Daher R, Badra R, el Rafei R, Bejjany R, Charafeddine L, Yunis K. Farra C, et al. Among authors: daher r. Biomed Res Int. 2015;2015:517679. doi: 10.1155/2015/517679. Epub 2015 Mar 5. Biomed Res Int. 2015. PMID: 25834820 Free PMC article.

3

Dietary Zinc Intake and Plasma Zinc Concentrations in Children with Short Stature and Failure to Thrive.

Yazbeck N, Hanna-Wakim R, El Rafei R, Barhoumi A, Farra C, Daher RT, Majdalani M. Yazbeck N, et al. Among authors: daher rt. Ann Nutr Metab. 2016;69(1):9-14. doi: 10.1159/000447648. Epub 2016 Jul 8. Ann Nutr Metab. 2016. PMID: 27387367

4

Cardiovascular disease biomarkers in patients with inborn errors of protein metabolism: a pilot study.

Karam PE, Majdalani MN, Daher RT, Barhoumi A, Yazbeck N. Karam PE, et al. Among authors: daher rt. J Hum Nutr Diet. 2015 Aug;28(4):344-9. doi: 10.1111/jhn.12255. Epub 2014 Jun 27. J Hum Nutr Diet. 2015. PMID: 24976504

5

False-negative primary neonatal thyroid screening: the need for clinical vigilance and secondary screening.

Yunis KA, Nasr MR, Lepejian G, Najjar S, Daher R. Yunis KA, et al. Among authors: daher r. J Med Screen. 2003;10(1):2-4. doi: 10.1258/096914103321610725. J Med Screen. 2003. PMID: 12790307

6

Higher Incidence Rates of Hypothyroidism and Late TSH Rise in Preterm Very-Low-Birth-Weight Infants at a Tertiary Care Center.

Tfayli H, Charafeddine L, Tamim H, Saade J, Daher RT, Yunis K. Tfayli H, et al. Horm Res Paediatr. 2018;89(4):224-232. doi: 10.1159/000487637. Epub 2018 Apr 11. Horm Res Paediatr. 2018. PMID: 29642061

7

A neonatal screening in Lebanon: Results of five years' experience.

Daher R, Beaini M, Mahfouz R, Cortas N, Younis KA. Daher R, et al. Ann Saudi Med. 2003 Jan-Mar;23(1-2):16-9. doi: 10.5144/0256-4947.2003.16. Ann Saudi Med. 2003. PMID: 17146215 Free article.

8

ApoB-100 R3500Q mutation in the Lebanese population: prevalence and historical review of the literature.

Sabbagh AS, Daher RT, Otrock ZK, Khalek RN, Zaatari GS, Mahfouz RA. Sabbagh AS, et al. Among authors: daher rt. Mol Biol Rep. 2007 Dec;34(4):267-70. doi: 10.1007/s11033-006-9041-7. Epub 2006 Dec 8. Mol Biol Rep. 2007. PMID: 17160438 Review.

9

High prevalence of MTHFR gene A1298C polymorphism in Lebanon.

Sabbagh AS, Mahfoud Z, Taher A, Zaatari G, Daher R, Mahfouz RA. Sabbagh AS, et al. Among authors: daher r. Genet Test. 2008 Mar;12(1):75-80. doi: 10.1089/gte.2007.0064. Genet Test. 2008. PMID: 18373406

10

Should we screen for hereditary hemochromatosis in healthy Lebanese: a pilot study.

Mahfouz RA, Sarieddine DS, Charafeddine KM, Abdul Khalik RN, Cortas NK, Daher RT. Mahfouz RA, et al. Among authors: daher rt. Mol Biol Rep. 2012 Jan;39(1):753-9. doi: 10.1007/s11033-011-0795-1. Epub 2011 May 7. Mol Biol Rep. 2012. PMID: 21553046

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