Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort
Jullien, Nicolas; Saveanu, Alexandru; Vergier, Julia; Marquant, Emeline; Quentien, Marie Helene; Castinetti, Frederic; Galon-Faure, Noémie; Brauner, Raja; Marrakchi Turki, Zinet; Tauber, Maité; El Kholy, Mohamed; Linglart, Agnès; Rodien, Patrice; Fedala, Nora Soumeya; Bergada, Ignacio; Cortet-Rudelli, Christine; Polak, Michel; Nicolino, Marc; Stuckens, Chantal; Barlier, Anne; Brue, Thierry; Reynaud, Rachel;
Abstract
The international GENHYPOPIT network collects phenotypical data and screens genetic causes of non-acquired hypopituitarism.
Other data
| Title | Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort | Authors | Jullien, Nicolas; Saveanu, Alexandru; Vergier, Julia; Marquant, Emeline; Quentien, Marie Helene; Castinetti, Frederic; Galon-Faure, Noémie; Brauner, Raja; Marrakchi Turki, Zinet; Tauber, Maité; El Kholy, Mohamed ; Linglart, Agnès; Rodien, Patrice; Fedala, Nora Soumeya; Bergada, Ignacio; Cortet-Rudelli, Christine; Polak, Michel; Nicolino, Marc; Stuckens, Chantal; Barlier, Anne; Brue, Thierry; Reynaud, Rachel | Keywords | ACTH deficiency; HESX1; LHX3; LHX4; Next-Generation Sequencing; OTX2; POU1F1; PROKR2; PROP1; TBX19; candidate gene approach; central hypothyroidism; congenital hypopituitarism; genetic screening; growth hormone deficiency; hypogonadotroph hypogonadism; ocular defect; panhypopituitarism; pituitary development; pituitary stalk interruption; transcription factor | Issue Date | 2021 | Publisher | WILEY | Journal | Clinical endocrinology | ISSN | 0300-0664 | DOI | 10.1111/cen.14355 | PubMed ID | 33098107 | Scopus ID | 2-s2.0-85100070228 | Web of science ID | WOS:000600578300001 |
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