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Zeitschriftenartikel
Vaczlavik, Anna; Bouys, Lucas; Violon, Florian; Giannone, Gaetan; Jouinot, Anne; Armignacco, Roberta; Cavalcante, Isadora P.; Berthon, Annabel; Letouze, Eric; Vaduva, Patricia; Barat, Maxime; Bonnet, Fideline; Perlemoine, Karine; Ribes, Christopher; Sibony, Mathilde; North, Marie-Odile; Espiard, Stephanie; Emy, Philippe; Haissaguerre, Magalie; Tauveron, Igor; Guignat, Laurence; Groussin, Lionel; Dousset, Bertrand; Reincke, Martin; Fragoso, Maria C.; Stratakis, Constantine A.; Pasmant, Eric; Libe, Rossella; Assie, Guillaume; Ragazzon, Bruno und Bertherat, Jerome
(2022):
KDM1A inactivation causes hereditary food-dependent Cushing syndrome.
In: Genetics in Medicine, Bd. 24, Nr. 2: S. 374-383
Cavalcante, Isadora P.; Berthon, Annabel; Fragoso, Maria C.; Reincke, Martin; Stratakis, Constantine A.; Ragazzon, Bruno und Bertherat, Jerome
(2022):
Primary bilateral macronodular adrenal hyperplasia: definitely a genetic disease.
In: Nature Reviews Endocrinology, Bd. 18, Nr. 11: S. 699-711
Perez-Rivas, Luis G.; Theodoropoulou, Marily; Puar, Troy H.; Fazel, Julia; Stieg, Mareike R.; Ferrau, Francesco; Assie, Guillaume; Gadelha, Monica R.; Deutschbein, Timo; Fragoso, Maria C.; Kusters, Benno; Saeger, Wolfgang; Honegger, Jürgen; Buchfelder, Michael; Korbonits, Marta; Bertherat, Jerome; Stalla, Guenter K.; Hermus, Ad R.; Beuschlein, Felix und Reincke, Martin
(2018):
Somatic USP8 mutations are frequent events in corticotroph tumor progression causing Nelson's tumor.
In: European Journal of Endocrinology, Bd. 178, Nr. 1: S. 57-63