Anzahl der Publikationen: 4
Zeitschriftenartikel
Geis, Tobias; Roedl, Tanja; Topaloglu, Haluk; Balci-Hayta, Burcu; Hinreiner, Sophie; Müller-Felber, Wolfgang; Schoser, Benedikt; Mehraein, Yasmin; Hübner, Angela; Zirn, Birgit; Hoopmann, Markus; Reutter, Heiko; Mowat, David; Schuierer, Gerhard; Schara, Ulrike; Hehr, Ute und Koelbel, Heike
(2019):
Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disorders.
In: Orphanet Journal of Rare Diseases, Bd. 14, 179
Chamova, Teodora; Bichev, Stoyan; Todorov, Tihomir; Gospodinova, Mariana; Taneva, Ani; Kastreva, Kristina; Zlatareva, Dora; Krupev, Martin; Hadjiivanov, Rosen; Guergueltcheva, Velina; Grozdanova, Liliana; Tzoneva, Dochka; Hübner, Angela; Hagen, Maja von der; Schoser, Benedikt; Lochmüller, Hanns; Todorova, Albena und Tournev, Ivailo
(2018):
Limb girdle muscular dystrophy 2G in a religious minority of Bulgarian Muslims homozygous for the c.75G > A, p.Trp25X mutation.
In: Neuromuscular Disorders, Bd. 28, Nr. 8: S. 625-632
Pamporaki, Christina; Hamplova, Barbora; Peitzsch, Mirko; Prejbisz, Aleksander; Beuschlein, Felix; Timmers, Henri J. L. M.; Fassnacht, Martin; Klink, Barbara; Lodish, Maya; Stratakis, Constantine A.; Hübner, Angela; Fliedner, Stephanie; Robledo, Mercedes; Sinnott, Richard O.; Januszewicz, Andrzej; Pacak, Karel und Eisenhofer, Graeme
(2017):
Characteristics of Pediatric vs Adult Pheochromocytomas and Paragangliomas.
In: Journal of Clinical Endocrinology & Metabolism, Bd. 102, Nr. 4: S. 1122-1132
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