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  • Jérôme Nevoux, Say Viengchareun, Ingrid Lema, A. L. Lecoq, Evelyne Ferrary, Marc Lombès
  • Chemistry, Medicine
  • Pflügers Archiv - European Journal of Physiology
  • 2014 (First Published: 1 September 2015)
  • Menière’s disease, clinically characterized by fluctuating, recurrent, and invalidating vertigo, hearing loss, and tinnitus, is linked to an increase in endolymph volume, the so-called endolymphaticContinue Reading
  • A. L. Lecoq, Jérôme Bouligand, +7 authors Peter Kamenický
  • Medicine
  • European journal of endocrinology
  • 2016 (First Published: 2 January 2016)
  • CONTEXT Recently, germline and somatic GPR101 p.(E308D) mutation was found in patients with isolated acromegaly. It is not known whether GPR101 point mutations are associated with other histologicalContinue Reading
  • Roberto Salvatori, Serban Radian, +23 authors Márta Korbonits
  • Medicine
  • European journal of endocrinology
  • 2017 (First Published: 1 September 2017)
  • OBJECTIVE Mutations in the aryl hydrocarbon receptor-interacting protein (AIP) gene are associated with pituitary adenoma, acromegaly and gigantism. Identical alleles in unrelated pedigrees could beContinue Reading
  • A. L. Lecoq, Sylvie Brailly-Tabard, +8 authors Peter Kamenický
  • Medicine
  • 2017 (First Published: 1 September 2017)
  • Contexte L’hypophosphatemie genetique hereditaire (HGH) s’accompagne d’une production excessive de FGF23 ayant pour consequence une perte renale de phosphore. Le traitement de l’HGH repose sur lesContinue Reading