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Items: 1 to 20 of 57

1.

Limitations of platform assays to measure serum 25OHD level impact on guidelines and practice decision making.

Rahme M, Al Shaar L, Singh R, Baddoura R, Halaby G, Arabi A, Habib RH, Daher R, Bassil D, El-Ferkh K, Hoteit M, Fuleihan GE.

Metabolism. 2018 Sep 15. pii: S0026-0495(18)30184-7. doi: 10.1016/j.metabol.2018.09.003. [Epub ahead of print]

PMID:
30227144
2.

Impact of Calcium and Two Doses of Vitamin D on Bone Metabolism in the Elderly: A Randomized Controlled Trial.

Rahme M, Sharara SL, Baddoura R, Habib RH, Halaby G, Arabi A, Singh RJ, Kassem M, Mahfoud Z, Hoteit M, Daher RT, Bassil D, El Ferkh K, El-Hajj Fuleihan G.

J Bone Miner Res. 2017 Jul;32(7):1486-1495. doi: 10.1002/jbmr.3122. Epub 2017 May 18.

3.

SERUM INSULIN-LIKE GROWTH FACTOR 1 IN LEBANESE SCHOOLCHILDREN AND ITS RELATION TO VITAMIN D AND FERRITIN LEVELS.

Gannagé-Yared MH, Chahine E, Farah V, Ibrahim T, Asmar N, Halaby G.

Endocr Pract. 2017 Apr 2;23(4):391-398. doi: 10.4158/EP161623.OR. Epub 2017 Jan 17.

PMID:
28095043
4.

Effect of vitamin D replacement on indexes of insulin resistance in overweight elderly individuals: a randomized controlled trial.

El-Hajj Fuleihan G, Baddoura R, Habib RH, Halaby G, Arabi A, Rahme M, Singh RJ, Kassem M, Mahfoud Z, Hoteit M, Daher RT, Kassir MF.

Am J Clin Nutr. 2016 Aug;104(2):315-23. doi: 10.3945/ajcn.116.132589. Epub 2016 Jul 13. Erratum in: Am J Clin Nutr. 2017 Apr;105(4):1021.

5.

[Screening of diabetic retinopathy and maculopathy in Lebanese population using retinography and SD-OCT: The role of telemedicine].

Chelala E, Saleh N, Dirani A, Fadlallah A, Baz P, Slim E, Halaby G, Bejjani R.

J Med Liban. 2015 Apr-Jun;63(2):59-65. French.

PMID:
26164973
6.

Estrogen receptor α is not a candidate gene for metabolic syndrome in Caucasian elderly subjects.

Hoteit M, Arabi A, Habib R, Mahfouz R, Baddoura R, Halaby G, El-Hajj Fuleihan G.

Metabolism. 2014 Jan;63(1):50-60. doi: 10.1016/j.metabol.2013.08.004. Epub 2013 Oct 17.

PMID:
24140101
7.

A novel ALMS1 splice mutation in a non-obese juvenile-onset insulin-dependent syndromic diabetic patient.

Sanyoura M, Woudstra C, Halaby G, Baz P, Senée V, Guillausseau PJ, Zalloua P, Julier C.

Eur J Hum Genet. 2014 Jan;22(1):140-3. doi: 10.1038/ejhg.2013.87. Epub 2013 May 8.

8.

Chronic urticaria and autoimmune thyroiditis.

Irani C, Jammal M, Asmar G, Hajj H, Halaby G.

J Med Liban. 2012 Apr-Jun;60(2):88-90.

PMID:
22919863
9.

Genetics of autoimmune thyroid disease in the Lebanese population.

Farra C, Awwad J, Fadlallah A, Sebaly G, Hage G, Souaid M, Ashkar H, Medlej R, Gannageh MH, Halaby G.

J Community Genet. 2012 Oct;3(4):259-64. doi: 10.1007/s12687-012-0085-1. Epub 2012 Mar 6.

10.

High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas.

Tichomirowa MA, Barlier A, Daly AF, Jaffrain-Rea ML, Ronchi C, Yaneva M, Urban JD, Petrossians P, Elenkova A, Tabarin A, Desailloud R, Maiter D, Schürmeyer T, Cozzi R, Theodoropoulou M, Sievers C, Bernabeu I, Naves LA, Chabre O, Montañana CF, Hana V, Halaby G, Delemer B, Aizpún JI, Sonnet E, Longás AF, Hagelstein MT, Caron P, Stalla GK, Bours V, Zacharieva S, Spada A, Brue T, Beckers A.

Eur J Endocrinol. 2011 Oct;165(4):509-15. doi: 10.1530/EJE-11-0304. Epub 2011 Jul 13.

11.

[Vitamin D status in Lebanese university students].

Gannagé-Yared MH, Chedid R, Halaby G.

J Med Liban. 2010 Oct-Dec;58(4):191-4.

PMID:
21409940
12.

Serum uric acid in relation with the metabolic syndrome components and adiponectin levels in Lebanese University students.

Chedid R, Zoghbi F, Halaby G, Gannagé-Yared MH.

J Endocrinol Invest. 2011 Jul-Aug;34(7):e153-7. doi: 10.3275/7350. Epub 2010 Nov 16.

PMID:
21088472
13.

[Mitral valve endocarditis complicated by septic pulmonary emboli].

Hajje G, Jebara V, Haddad A, Aoun N, Halaby G.

Med Mal Infect. 2011 Mar;41(3):154-5. doi: 10.1016/j.medmal.2010.09.019. Epub 2010 Nov 18. French. No abstract available.

PMID:
21087831
14.

Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative study.

Daly AF, Tichomirowa MA, Petrossians P, Heliövaara E, Jaffrain-Rea ML, Barlier A, Naves LA, Ebeling T, Karhu A, Raappana A, Cazabat L, De Menis E, Montañana CF, Raverot G, Weil RJ, Sane T, Maiter D, Neggers S, Yaneva M, Tabarin A, Verrua E, Eloranta E, Murat A, Vierimaa O, Salmela PI, Emy P, Toledo RA, Sabaté MI, Villa C, Popelier M, Salvatori R, Jennings J, Longás AF, Labarta Aizpún JI, Georgitsi M, Paschke R, Ronchi C, Valimaki M, Saloranta C, De Herder W, Cozzi R, Guitelman M, Magri F, Lagonigro MS, Halaby G, Corman V, Hagelstein MT, Vanbellinghen JF, Barra GB, Gimenez-Roqueplo AP, Cameron FJ, Borson-Chazot F, Holdaway I, Toledo SP, Stalla GK, Spada A, Zacharieva S, Bertherat J, Brue T, Bours V, Chanson P, Aaltonen LA, Beckers A.

J Clin Endocrinol Metab. 2010 Nov;95(11):E373-83. doi: 10.1210/jc.2009-2556. Epub 2010 Aug 4.

15.

[Autoimmune thyroid disease. Clinical and biological correlations].

El Hajj G, Yahya AF, Medlej R, Sebaaly G, Souaid M, Halaby G.

J Med Liban. 2009 Oct-Dec;57(4):218-25. French.

PMID:
20027797
16.

Multiple pancreatic insulinomas: multislice CT.

Menassa-Moussa L, Halaby G, Braidy C.

Abdom Imaging. 2010 Dec;35(6):690-3. doi: 10.1007/s00261-009-9585-9.

PMID:
19885635
17.

Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency.

Metherell LA, Naville D, Halaby G, Begeot M, Huebner A, Nürnberg G, Nürnberg P, Green J, Tomlinson JW, Krone NP, Lin L, Racine M, Berney DM, Achermann JC, Arlt W, Clark AJ.

J Clin Endocrinol Metab. 2009 Oct;94(10):3865-71. doi: 10.1210/jc.2009-0467. Epub 2009 Sep 22.

18.

Impact of different metabolic syndrome classifications on the metabolic syndrome prevalence in a young Middle Eastern population.

Chedid R, Gannagé-Yared MH, Khalifé S, Halaby G, Zoghbi F.

Metabolism. 2009 Jun;58(6):746-52. doi: 10.1016/j.metabol.2008.11.014.

PMID:
19446111
19.

Predictors of intra-operative parathyroid hormone decline in subjects operated for primary hyperparathyroidism by minimally invasive parathyroidectomy.

Gannagé-Yared MH, Abboud B, Amm-Azar M, Saab A, Khalife S, Halaby G, Atallah C, Medlej R, Jambart S.

J Endocrinol Invest. 2009 Feb;32(2):160-4.

PMID:
19411816
20.

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.

Hum Mutat. 2009 Jul;30(7):E682-91. doi: 10.1002/humu.21002.

PMID:
19319977

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