Marie-Hélène Quentien

Mutations in NFKB2and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

Thierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian et al. · BMC Medical Genetics · 2014 · 93 citations · Full text

Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections

Marie-Hélène Quentien, Brigitte Delemer, Dimitrios T. Papadimitriou et al. · The Journal of Clinical Endocrinology & Metabolism · 2011 · 60 citations · Full text

Regulation of Prolactin, GH, and Pit-1 Gene Expression in Anterior Pituitary by Pitx2: An Approach Using Pitx2 Mutants

Marie-Hélène Quentien, Fabián Pitoia, Ginette Gunz et al. · Endocrinology · 2002 · 47 citations

Human Growth, Genetics, Pituitary Cell Lines +19

Pitx Factors Are Involved in Basal and Hormone-regulated Activity of the Human Prolactin Promoter

Marie-Hélène Quentien, Isabelle Manfroid, Daniel Moncet et al. · Journal of Biological Chemistry · 2002 · 44 citations · Full text

Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency

Nicolas Jullien, Pauline Romanet, Mélanie Philippon et al. · European Journal of Human Genetics · 2018 · 27 citations · Full text

Developmental Biology, Pituitary Gland, Growth Hormone +9