Dimitrios T. Papadimitriou

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

Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism

Lucie Pujo, Jérôme Fagart, Françoise Gary et al. · Human Mutation · 2006 · 88 citations

Hypertension, Compensatory Aldosterone Excess, Electrolyte Disorder +21

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

Puberty in Subjects with Complete Androgen Insensitivity Syndrome

Dimitrios T. Papadimitriou, Agnès Linglart, Yves Morel et al. · Hormone Research in Paediatrics · 2006 · 59 citations

The Big Vitamin D Mistake

Dimitrios T. Papadimitriou · Journal of Preventive Medicine and Public Health · 2017 · 41 citations · Full text

Nutrition, Nutritional Epidemiology, Nutrition Development +20