Gannagé-Yared MH - Search Results

1

Homozygous mutation of the IGF1 receptor gene in a patient with severe pre- and postnatal growth failure and congenital malformations.

Gannagé-Yared MH, Klammt J, Chouery E, Corbani S, Mégarbané H, Abou Ghoch J, Choucair N, Pfäffle R, Mégarbané A. Gannagé-Yared MH, et al. Eur J Endocrinol. 2012 Dec 10;168(1):K1-7. doi: 10.1530/EJE-12-0701. Print 2013 Jan. Eur J Endocrinol. 2012. PMID: 23045302

2

Primary hypergonadotropic hypogonadism, partial alopecia, and Müllerian hypoplasia: report of a second family with additional findings.

Mégarbané A, Gannagé-Yared MH, Khalifé AA, Fabre M. Mégarbané A, et al. Am J Med Genet A. 2003 Jun 1;119A(2):214-7. doi: 10.1002/ajmg.a.20170. Am J Med Genet A. 2003. PMID: 12749067

3

Coexistence of Kallmann syndrome and complete androgen insensitivity in the same patient.

Gannagé-Yared MH, Dodé C, Ghanem I, Chouery E, Jalkh N, Hardelin JP, Mégarbané A. Gannagé-Yared MH, et al. Eur J Endocrinol. 2005 Jun;152(6):813-7. doi: 10.1530/eje.1.01915. Eur J Endocrinol. 2005. PMID: 15941919

4

Exome sequencing reveals a mutation in DMP1 in a family with familial sclerosing bone dysplasia.

Gannagé-Yared MH, Makrythanasis P, Chouery E, Sobacchi C, Mehawej C, Santoni FA, Guipponi M, Antonarakis SE, Hamamy H, Mégarbané A. Gannagé-Yared MH, et al. Bone. 2014 Nov;68:142-5. doi: 10.1016/j.bone.2014.08.014. Epub 2014 Aug 30. Bone. 2014. PMID: 25180662

5

Relationship between vitamin D receptor gene polymorphisms, cardiovascular risk factors and adiponectin in a healthy young population.

Hajj A, Chedid R, Chouery E, Megarbané A, Gannagé-Yared MH. Hajj A, et al. Pharmacogenomics. 2016 Oct;17(15):1675-1686. doi: 10.2217/pgs-2016-0045. Epub 2016 Sep 27. Pharmacogenomics. 2016. PMID: 27672714 Free article.

6

A Comprehensive Cohort Analysis Comparing Growth and GH Therapy Response in IGF1R Mutation Carriers and SGA Children.

Göpel E, Rockstroh D, Pfäffle H, Schlicke M, Pozza SB, Gannagé-Yared MH, Gucev Z, Mohn A, Harmel EM, Volkmann J, Weihrauch-Blüher S, Gausche R, Bogatsch H, Beger C, Klammt J, Pfäffle R. Göpel E, et al. J Clin Endocrinol Metab. 2020 Apr 1;105(4):dgz165. doi: 10.1210/clinem/dgz165. J Clin Endocrinol Metab. 2020. PMID: 31680140

7

Serum adiponectin and leptin levels in relation to the metabolic syndrome, androgenic profile and somatotropic axis in healthy non-diabetic elderly men.

Gannagé-Yared MH, Khalife S, Semaan M, Fares F, Jambart S, Halaby G. Gannagé-Yared MH, et al. Eur J Endocrinol. 2006 Jul;155(1):167-76. doi: 10.1530/eje.1.02175. Eur J Endocrinol. 2006. PMID: 16793964

8

Osteoprotegerin in relation to body weight, lipid parameters insulin sensitivity, adipocytokines, and C-reactive protein in obese and non-obese young individuals: results from both cross-sectional and interventional study.

Gannagé-Yared MH, Yaghi C, Habre B, Khalife S, Noun R, Germanos-Haddad M, Trak-Smayra V. Gannagé-Yared MH, et al. Eur J Endocrinol. 2008 Mar;158(3):353-9. doi: 10.1530/EJE-07-0797. Eur J Endocrinol. 2008. PMID: 18299469

9

Vitamin D in relation to metabolic risk factors, insulin sensitivity and adiponectin in a young Middle-Eastern population.

Gannagé-Yared MH, Chedid R, Khalife S, Azzi E, Zoghbi F, Halaby G. Gannagé-Yared MH, et al. Eur J Endocrinol. 2009 Jun;160(6):965-71. doi: 10.1530/EJE-08-0952. Epub 2009 Mar 16. Eur J Endocrinol. 2009. PMID: 19289535

10

The molecular basis of familial hypercholesterolemia in Lebanon: spectrum of LDLR mutations and role of PCSK9 as a modifier gene.

Abifadel M, Rabès JP, Jambart S, Halaby G, Gannagé-Yared MH, Sarkis A, Beaino G, Varret M, Salem N, Corbani S, Aydénian H, Junien C, Munnich A, Boileau C. Abifadel M, et al. Hum Mutat. 2009 Jul;30(7):E682-91. doi: 10.1002/humu.21002. Hum Mutat. 2009. PMID: 19319977

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