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The Journal of Clinical Endocrinology and Metabolism|January 13, 2012
Symptomatic heterozygotes and prenatal diagnoses in a nonconsanguineous family with syndromic combined pituitary hormone deficiency resulting from two novel LHX3 mutationsMarie-Laure Sobrier, Cécile Brachet, Marie-Pierre Vié-Luton, et al.Clinical Biochemistry|November 14, 2016
Concordance between CRP and SAA in familial Mediterranean fever during attack-free period: A study of 218 patientsKatia Stankovic Stojanovic, Véronique Hentgen, Soraya Fellahi, et al.Current Drug Targets. Inflammation and Allergy|February 22, 2005
Amyloidosis and auto-inflammatory syndromesGilles Grateau, Isabelle Jéru, Saad Rouaghe, et al.European Journal of Endocrinology|April 27, 2012
Screening of LHX2 in patients presenting growth retardation with posterior pituitary and ocular abnormalitiesChristelle Pérez, Florence Dastot-Le Moal, Nathalie Collot, et al.Pharmacology & Therapeutics|February 22, 2018
Inflammasome biology, molecular pathology and therapeutic implicationsFawaz Awad, Eman Assrawi, Camille Louvrier, et al.Plos One|November 6, 2009
Involvement of the modifier gene of a human Mendelian disorder in a negative selection processIsabelle Jéru, Hasmik Hayrapetyan, Philippe Duquesnoy, et al.The Journal of Clinical Endocrinology and Metabolism|April 5, 2007
Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous statesPeng Fang, Stefan Riedl, Serge Amselem, et al.Arthritis and Rheumatism|April 12, 2011
Role of interleukin-1β in NLRP12-associated autoinflammatory disorders and resistance to anti-interleukin-1 therapyIsabelle Jéru, Véronique Hentgen, Sylvain Normand, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|January 13, 2015
The c.301_302delAG PROP1 gene mutation in Romanian patients with multiple pituitary hormone deficiencyCecilia Lazea, Paula Grigorescu-Sido, Radu Popp, et al.Plos One|July 12, 2013
The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approachIsabelle Jéru, Véronique Hentgen, Emmanuelle Cochet, et al.Pageof 13