Zobrazeno 1 - 10
of 208
pro vyhledávání: '"Stephan Petersenn"'
Autor:
Stephan Petersenn
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 148:371-379
Autor:
Stephan Petersenn
Publikováno v:
Pituitary. 25:693-697
Initial pathology in aggressive pituitary tumours and carcinomas: 2b or not 2b?-that is the question
Autor:
Jacqueline Trouillas, Pia Burman, Marco Losa, Ann McCormack, Stephan Petersenn, Vera Popovic, Marily Theodoropoulou, Olaf M Dekkers, Gerald Raverot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a4c861f301a9b3a49880721508af16d
https://hdl.handle.net/1887/3619444
https://hdl.handle.net/1887/3619444
Autor:
Maria Fleseriu, Ariel Barkan, Maria del Pilar Schneider, Yannis Darhi, Amicie de Pierrefeu, Antonio Ribeiro-Oliveira, Stephan Petersenn, Sebastian Neggers, Shlomo Melmed
Publikováno v:
Pituitary, 25(2), 296-307. Kluwer Academic
Purpose Patients receiving treatment for acromegaly often experience significant associated comorbidities for which they are prescribed additional medications. We aimed to determine the real-world prevalence of comorbidities and concomitant medicatio
Publikováno v:
Pituitary
Purpose PRIMARYS (NCT00690898) was a 48-week, open-label, phase 3b study, evaluating treatment with the somatostatin receptor ligand lanreotide autogel (stable dose: 120 mg/28 days) in treatment-naïve patients with growth hormone (GH)-secreting pitu
Autor:
Stephan Petersenn
Publikováno v:
Pituitary. 23:9-15
Prolactinomas are the most frequently seen pituitary adenomas in clinical practice. A correct biochemical diagnosis of hyperprolactinemia is a prerequisite for further investigation but may be hampered by analytical difficulties as well as a large nu
Autor:
Stephan Petersenn
Publikováno v:
Hormone and Metabolic Research. 51:755-764
With a prevalence of 80–100/100000, pituitary adenomas are more frequent than thought. The rare aggressive pituitary adenoma presents a special challenge, due to the heterogenous presentation of the disease. The prognosis of aggressive pituitary ad
Autor:
Bettina Stamm, Stephan Petersenn, Matthias M. Weber, Heide Siggelkow, Georg Brabant, Stephan H. Scharla, Jörg Bojunga, Gwendolin Etzrodt-Walter, Corinna Wicke, R. Finke
Publikováno v:
MMW - Fortschritte der Medizin. 161:12-20
Hypoparathyreoidismus ist eine seltene und den Patienten beeintrachtigende Erkrankung, die durch eine Hypokalzamie in Verbindung mit einem niedrigen Parathormon gekennzeichnet ist. Meist ist sie Folge der Entfernung oder Verletzung der Nebenschilddru
Autor:
Stylianos Tsagarakis, Ashley B. Grossman, André Lacroix, Maria Chiara Zatelli, Hershel Raff, Lynnette K. Nieman, Eliza B Geer, Cesar Luiz Boguszewski, Beverly M. K. Biller, Marily Theodoropoulou, Mark E. Molitch, Daniel F. Kelly, Alberto M. Pereira, Marcello D. Bronstein, Brooke Swearingen, Stephan Petersenn, Irina Bancos, Adriana G. Ioachimescu, Frederic Castinetti, Ken K. Y. Ho, Ilan Shimon, Martin Reincke, Susan M. Webb, Richard J. Auchus, John Newell-Price, Roberto Salvatori, Shlomo Melmed, Carla Scaroni, Maria Fleseriu, Ursula B. Kaiser, Greisa Vila, Jérôme Bertherat, Anat Ben-Shlomo, Andrea Giustina, Mônica R. Gadelha, Michael Buchfelder, James W. Findling, Mark Gurnell, Rosario Pivonello, Philippe Chanson, Yutaka Takahashi, John A.H. Wass, Nienke R. Biermasz, Ann McCormack, Niki Karavitaki, Felipe F. Casanueva, Laurence Katznelson, Elena Valassi, Antoine Tabarin, John D. Carmichael, Pietro Mortini, Constantine A. Stratakis, Elena V. Varlamov
Publikováno v:
Lancet Diabetes Endocrinol
Lancet Diabetes & Endocrinology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
The Lancet Diabetes and Endocrinology, 9(12), 847-875. ELSEVIER SCIENCE INC
Lancet Diabetes & Endocrinology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
The Lancet Diabetes and Endocrinology, 9(12), 847-875. ELSEVIER SCIENCE INC
Summary Cushing's disease requires accurate diagnosis, careful treatment selection, and long-term management to optimise patient outcomes. The Pituitary Society convened a consensus workshop comprising more than 50 academic researchers and clinical e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b02c984bd7cbf20d049ef42e0bca6d7
https://europepmc.org/articles/PMC8743006/
https://europepmc.org/articles/PMC8743006/
Autor:
Ulrich J. Knappe, Juergen Honegger, Joerg Flitsch, Dag Moskopp, Klaus Christian Mende, Rocío Evangelista-Zamora, Stephan Petersenn, Timo Deutschbein, Michael Droste, Teresa Kellner, Yawen Wang, Katharina Schilbach, Guenter K. Stalla
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:252-265
Context Craniopharyngioma is a rare neoplastic entity of the central nervous system. Childhood-onset craniopharyngioma is the subject of frequent research whereas the information on adult-onset craniopharyngioma is scarce. Objective The objective of