Jambart S - Search Results

1

Craniofacial anomalies, deafness, brachydactyly, short stature, and moderate mental retardation due to a cryptic 6p;11q translocation.

Mégarbané A, Bejjani BA, Shaffer LG, Jambart S, Souraty N, Kashork CD, Le Merrer M. Mégarbané A, et al. Among authors: jambart s. Am J Med Genet. 2002 Feb 15;108(1):69-74. doi: 10.1002/ajmg.10222. Am J Med Genet. 2002. PMID: 11857553

2

Prevalence of painful diabetic peripheral neuropathy among patients with diabetes mellitus in the Middle East region.

Jambart S, Ammache Z, Haddad F, Younes A, Hassoun A, Abdalla K, Selwan CA, Sunna N, Wajsbrot D, Youseif E. Jambart S, et al. J Int Med Res. 2011;39(2):366-77. doi: 10.1177/147323001103900204. J Int Med Res. 2011. PMID: 21672340 Free article.

3

Low circulating PCSK9 levels in LPL homozygous children with chylomicronemia syndrome in a syrian refugee family in Lebanon.

Ayoub C, Azar Y, Maddah D, Ghaleb Y, Elbitar S, Abou-Khalil Y, Jambart S, Varret M, Boileau C, El Khoury P, Abifadel M. Ayoub C, et al. Among authors: jambart s. Front Genet. 2022 Aug 19;13:961028. doi: 10.3389/fgene.2022.961028. eCollection 2022. Front Genet. 2022. PMID: 36061186 Free PMC article.

4

Identification of the first Tangier disease patient in Lebanon carrying a new pathogenic variant in ABCA1.

El Khoury P, Couvert P, Elbitar S, Ghaleb Y, Abou-Khalil Y, Azar Y, Ayoub C, Superville A, Guérin M, Rabès JP, Varret M, Boileau C, Jambart S, Giral P, Carrié A, Le Goff W, Abifadel M. El Khoury P, et al. Among authors: jambart s. J Clin Lipidol. 2018 Nov-Dec;12(6):1374-1382. doi: 10.1016/j.jacl.2018.08.013. Epub 2018 Sep 1. J Clin Lipidol. 2018. PMID: 30361172

5

Identification of a Variant in APOB Gene as a Major Cause of Hypobetalipoproteinemia in Lebanese Families.

Ayoub C, Azar Y, Abou-Khalil Y, Ghaleb Y, Elbitar S, Halaby G, Jambart S, Gannagé-Yared MH, Yaghi C, Saade Riachy C, El Khoury R, Rabès JP, Varret M, Boileau C, El Khoury P, Abifadel M. Ayoub C, et al. Among authors: jambart s. Metabolites. 2021 Aug 24;11(9):564. doi: 10.3390/metabo11090564. Metabolites. 2021. PMID: 34564380 Free PMC article.

6

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. Among authors: jambart s. Hum Mutat. 2009 Jul;30(7):E682-91. doi: 10.1002/humu.21002. Hum Mutat. 2009. PMID: 19319977

7

Dyslipidaemia in the Middle East: Current status and a call for action.

Al Rasadi K, Almahmeed W, AlHabib KF, Abifadel M, Farhan HA, AlSifri S, Jambart S, Zubaid M, Awan Z, Al-Waili K, Barter P. Al Rasadi K, et al. Among authors: jambart s. Atherosclerosis. 2016 Sep;252:182-187. doi: 10.1016/j.atherosclerosis.2016.07.925. Epub 2016 Jul 30. Atherosclerosis. 2016. PMID: 27522462 Free article. Review.

8

Global perspective of familial hypercholesterolaemia: a cross-sectional study from the EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC).

EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC). EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC). Lancet. 2021 Nov 6;398(10312):1713-1725. doi: 10.1016/S0140-6736(21)01122-3. Epub 2021 Sep 7. Lancet. 2021. PMID: 34506743

9

[Significance of TSH receptor antibody determination].

Gannage MH, Haddad F, Jambart S, Atallah C, Halaby G. Gannage MH, et al. Among authors: jambart s. J Med Liban. 1996;44(3):134-7. J Med Liban. 1996. PMID: 9296963 French.

10

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. Gannagé-Yared MH, et al. Among authors: jambart s. J Endocrinol Invest. 2009 Feb;32(2):160-4. doi: 10.1007/BF03345707. J Endocrinol Invest. 2009. PMID: 19411816

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