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Springe zu: Zeitschriftenartikel
Anzahl der Publikationen: 3
Zeitschriftenartikel
Di Dalmazi, Guido; Timmers, Henri J. L. M.; Arnaldi, Giorgio; Kusters, Benno; Scarpelli, Marina; Bathon, Kerstin; Calebiro, Davide; Beuschlein, Felix; Hermus, Ad und Reincke, Martin
(2019):
Somatic PRKACA Mutations: Association With Transition From Pituitary-Dependent to Adrenal-Dependent Cushing Syndrome.
In: Journal of Clinical Endocrinology & Metabolism, Bd. 104, Nr. 11: S. 5651-5657
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
Maroofian, Reza; Riemersma, Moniek; Jae, Lucas T.; Zhianabed, Narges; Willemsen, Marjolein H.; Wissink-Lindhout, Willemijn M.; Willemsen, Michel A.; Brouwer, Arjan P. M. de; Mehrjardi, Mohammad Yahya Vahidi; Ashrafi, Mahmoud Reza; Kusters, Benno; Kleefstra, Tjitske; Jamshidi, Yalda; Nasseri, Mojila; Pfundt, Rolph; Brummelkamp, Thijn R.; Abbaszadegan, Mohammad Reza; Lefeber, Dirk J. und Bokhoven, Hans van
(2017):
B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies.
In: Genome Medicine
9:118
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