Mouna Barat-Houari

Mouna Barat-Houari

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Mouna Barat-Houari

Mouna Barat-Houari

Publications by authors named "Mouna Barat-Houari"

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B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation.

Genet Med 2018 02 3;20(2):269-274. Epub 2017 Aug 3.

Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, Centre de Référence Anomalies du Développement et Syndromes Malformatifs, Plateforme Recherche de Microremaniements Chromosomiques, Hôpital Arnaud de Villeneuve, CHU de Montpellier, Faculté de Médecine Montpellier-Nîmes, Université de Montpellier, Montpellier, France.

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http://dx.doi.org/10.1038/gim.2017.109DOI Listing
February 2018

Confirmation of autosomal recessive inheritance of COL2A1 mutations in spondyloepiphyseal dysplasia congenita: Lessons for genetic counseling.

Am J Med Genet A 2016 Jan 11;170A(1):263-5. Epub 2015 Sep 11.

Laboratoire de génétique des maladies rares et auto-inflammatoires, CHRU, Montpellier, France.

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http://dx.doi.org/10.1002/ajmg.a.37374DOI Listing
January 2016

Mutation Update for COL2A1 Gene Variants Associated with Type II Collagenopathies.

Hum Mutat 2016 Jan 21;37(1):7-15. Epub 2015 Oct 21.

Laboratory of Rare and Autoinflammatory Diseases, CHRU, Montpellier, France.

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http://dx.doi.org/10.1002/humu.22915DOI Listing
January 2016

Treatment of Erdheim-Chester disease with canakinumab.

Rheumatology (Oxford) 2014 Dec 17;53(12):2312-4. Epub 2014 Sep 17.

Department of Pediatrics, Nîmes University Hospital, Nîmes, INSERM U 844, University of Montpelier 1, Montpellier, Department of Pediatric Radiology, Department of Pediatrics, Assistance Publique Hôpitaux de Paris, Bicêtre University Hospital, Le Kremlin Bicêtre, University of Poitiers, Laboratoire Inflammation, Tissus Epithéliaux et Cytokines (LITEC) Poitiers, Laboratory of Genetics, Rare and Autoinflammatory Diseases, Department of Genetics, LBM - Montpellier University Hospital, INSERM U844, Montpellier and Department of General Pediatrics and Internal Medicine, Assistance Publique Hôpitaux de Paris, Robert Debré University Hospital, University of Paris, Paris, France.

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http://dx.doi.org/10.1093/rheumatology/keu344DOI Listing
December 2014

Dysspondyloenchondromatosis without COL2A1 mutation: possible genetic heterogeneity.

Am J Med Genet A 2014 Mar 19;164A(3):769-73. Epub 2013 Dec 19.

Département de Génétique Médicale, Centre de Référence Maladies Rares Anomalies du Développement et Syndromes Malformatifs Sud-Languedoc Roussillon, CHRU Montpellier, Faculté de Médecine Université Montpellier 1, Montpellier, France.

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http://dx.doi.org/10.1002/ajmg.a.36331DOI Listing
March 2014

Identification of a new exon 2-skipped TNFR1 transcript: regulation by three functional polymorphisms of the TNFR-associated periodic syndrome (TRAPS) gene.

Ann Rheum Dis 2014 Jan 16;73(1):290-7. Epub 2013 Mar 16.

Génétique des maladies Autoinflammatoires et des ostéoarthropathies chroniques, INSERM U844, Hôpital Saint Eloi, Bâtiment INM, , Montpellier, France.

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http://dx.doi.org/10.1136/annrheumdis-2012-203023DOI Listing
January 2014

Lack of TEK Gene Mutation in Patients with Cutaneomucosal Venous Malformations from the North-Western Region of Algeria.

Genet Res Int 2013 9;2013:784789. Epub 2013 Dec 9.

Unité Médicale des Maladies Auto-Inflammatoires, Département de Génétique, CHRU, Montpellier, 34961 Montpellier Cedex 2, France.

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http://dx.doi.org/10.1155/2013/784789DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3872160PMC
January 2014

Association Analysis of IL10, TNF-α, and IL23R-IL12RB2 SNPs with Behçet's Disease Risk in Western Algeria.

Front Immunol 2013 21;4:342. Epub 2013 Oct 21.

Laboratory of Applied Molecular Biology and Immunology. Department of Biology, Abou-Bekr Belkaïd University , Tlemcen , Algeria.

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http://dx.doi.org/10.3389/fimmu.2013.00342DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3801160PMC
October 2013

Kimura's disease and Behcet's syndrome in the same family--are they associated?

Joint Bone Spine 2013 Jan 29;80(1):44-7. Epub 2012 Jun 29.

Department of Medicine, Rheumatology Unit, Hadassah-Hebrew University Medical Center Head, POB 12000, Jerusalem, Israel.

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http://dx.doi.org/10.1016/j.jbspin.2012.04.001DOI Listing
January 2013

SNPs in the TNF-α gene promoter associated with Behcet's disease in Moroccan patients.

Rheumatology (Oxford) 2012 Sep 17;51(9):1595-9. Epub 2012 Jun 17.

Unité médicale des maladies Auto-inflammatoires, CHRU Montpellier, Hôpital A. de Villeneuve, 371 avenue du Doyen Gaston Giraud, Montpellier Cedex 5, France.

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http://dx.doi.org/10.1093/rheumatology/kes141DOI Listing
September 2012

Impact of a CART promoter genetic variation on plasma lipid profile in a general population.

Mol Genet Metab 2007 Feb 27;90(2):199-204. Epub 2006 Sep 27.

CNRS UMR 8090, Institut de Biologie de Lille, Institut Pasteur de Lille, 1 rue du Professeur Calmette, BP 245, 59019 Lille Cedex, France.

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http://dx.doi.org/10.1016/j.ymgme.2006.08.012DOI Listing
February 2007