Molar incisor hypomineralisation in Lebanon: prevalence and clinical characteristics
Elzein, R., Chouery, E., Abdel-Sater, F., Bacho, R., Ayoub, F.
Published in European archives of paediatric dentistry (01.10.2020)
Published in European archives of paediatric dentistry (01.10.2020)
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Journal Article
Molar–incisor hypomineralisation in Lebanon: association with prenatal, natal and postnatal factors
Elzein, R., Chouery, E., Abdel-Sater, F., Bacho, R., Ayoub, F.
Published in European archives of paediatric dentistry (01.04.2021)
Published in European archives of paediatric dentistry (01.04.2021)
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Journal Article
Identification by whole-exome sequencing of new single-nucleotide polymorphisms associated with molar-incisor hypomineralisation among the Lebanese population
Elzein, R., Abdel-Sater, F., Mehawej, C., Jalkh, N., Ayoub, F., Chouery, E.
Published in European archives of paediatric dentistry (01.12.2022)
Published in European archives of paediatric dentistry (01.12.2022)
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Journal Article
Deciphering balanced translocations in infertile males by next-generation sequencing to identify candidate genes for spermatogenesis disorders
Yammine, T, Reynaud, N, Lejeune, H, Diguet, F, Rollat-Farnier, P A, Labalme, A, Plotton, I, Farra, C, Sanlaville, D, Chouery, E, Schluth-Bolard, C
Published in Molecular human reproduction (29.05.2021)
Published in Molecular human reproduction (29.05.2021)
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Journal Article
Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene
Van Maldergem, L, Siitonen, H A, Jalkh, N, Chouery, E, De Roy, M, Delague, V, Muenke, M, Jabs, E W, Cai, J, Wang, L L, Plon, S E, Fourneau, C, Kestilä, M, Gillerot, Y, Mégarbané, A, Verloes, A
Published in Journal of medical genetics (01.02.2006)
Published in Journal of medical genetics (01.02.2006)
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Journal Article
A novel deletion in ZBTB24 in a Lebanese family with immunodeficiency, centromeric instability, and facial anomalies syndrome type 2
Chouery, E, Abou-Ghoch, J, Corbani, S, El Ali, N, Korban, R, Salem, N, Castro, C, Klayme, S, Azoury-Abou Rjeily, M, Khoury-Matar, R, Debo, G, Germanos-Haddad, M, Delague, V, Lefranc, G, Mégarbané, A
Published in Clinical genetics (01.11.2012)
Published in Clinical genetics (01.11.2012)
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Journal Article
Cardiorenal syndrome in hypertensive rats: microalbuminuria, inflammation and ventricular hypertrophy
Moubarak, M, Jabbour, H, Smayra, V, Chouery, E, Saliba, Y, Jebara, V, Fares, N
Published in Physiological research (01.01.2012)
Published in Physiological research (01.01.2012)
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Journal Article
A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22–q13.12
Chouery, E., Kfoury, J., Delague, V., Jalkh, N., Bejjani, P., Serre, J. L., Mégarbané, A.
Published in Neurogenetics (01.10.2008)
Published in Neurogenetics (01.10.2008)
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Journal Article
Molecular screening of MECP2 gene in a cohort of Lebanese patients suspected with Rett syndrome: report on a mild case with a novel indel mutation
Corbani, S., Chouery, E., Fayyad, J., Fawaz, A., El Tourjuman, O., Badens, C., Lacoste, C., Delague, V., Megarbane, A.
Published in Journal of intellectual disability research (01.04.2012)
Published in Journal of intellectual disability research (01.04.2012)
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Journal Article
Mild Campomelic Dysplasia: Report on a Case and Review
Corbani, S., Chouery, E., Eid, B., Jalkh, N., Abou Ghoch, J., Mégarbané, A.
Published in Molecular syndromology (01.01.2011)
Published in Molecular syndromology (01.01.2011)
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Journal Article
Molecular Study of Three Lebanese and Syrian Patients with Waardenburg Syndrome and Report of Novel Mutations in the EDNRB and MITF Genes
Haddad, N.M., Ente, D., Chouery, E., Jalkh, N., Mehawej, C., Khoueir, Z., Pingault, V., Mégarbané, A.
Published in Molecular syndromology (01.01.2011)
Published in Molecular syndromology (01.01.2011)
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Journal Article
Homozygosity mapping of autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy (CMT4H) to a novel locus on chromosome 12p11.21-q13.11
Sandre-Giovannoli, A De, Delague, V, Hamadouche, T, Chaouch, M, Krahn, M, Boccaccio, I, Maisonobe, T, Chouery, E, Jabbour, R, Atweh, S, Grid, D, Mégarbané, A, Lévy, N
Published in Journal of medical genetics (01.03.2005)
Published in Journal of medical genetics (01.03.2005)
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Journal Article
A new familial sclerosing bone dysplasia
Chouery, Eliane, Pangrazio, Alessandra, Frattini, Annalisa, Villa, Anna, Van Wesenbeeck, Liesbeth, Piters, Elke, Van Hul, Wim, Coxon, Fraser P, Schouten, Tabitha, Helfrich, Miep, Lefranc, Gérard, Mégarbané, André
Published in Journal of bone and mineral research (01.03.2010)
Published in Journal of bone and mineral research (01.03.2010)
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Journal Article
Microalbuminuria versus brain natriuretic peptide in cardiac hypertrophy of hypertensive rats
Saliba, Y, Chouery, E, Mégarbané, A, Jabbour, H, Farès, N
Published in Physiological research (01.01.2010)
Published in Physiological research (01.01.2010)
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Journal Article
Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation
DJAMBAS KHAYAT, C., SALEM, N., CHOUERY, E., CORBANI, S., MOIX, I., NICOLAS, E., MORRIS, M.A., DE MOERLOOSE, P., MÉGARBANÉ, A.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2008)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2008)
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Journal Article
Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene
Mustapha, Myrna, Salem, Nabiha, Delague, Valérie, Chouery, Eliane, Ghassibeh, Michella, Rai, Myriam, Loiselet, Jacques, Petit, Christine, Mégarbané, André
Published in Journal of medical genetics (01.10.2001)
Published in Journal of medical genetics (01.10.2001)
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Journal Article
B-type natriuretic peptide receptors in hypertrophied adult rat cardiomyocytes
Nader, L., Lahoud, L., Chouery, E., Aftimos, G., Bois, P., Farès, N.A.
Published in Annales de cardiologie et d'angeiologie (01.02.2010)
Published in Annales de cardiologie et d'angeiologie (01.02.2010)
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