Zobrazeno 1 - 10
of 417
pro vyhledávání: '"J, Knappe"'
Autor:
Anke Tönjes, Marleen Würfel, Marcus Quinkler, Ulrich J. Knappe, Jürgen Honegger, Nina Krause-Joppig, Konrad Bacher, Timo Deutschbein, Sylvère Störmann, Jochen Schopohl, Sebastian M. Meyhöfer, the participants of the German Acromegaly Registry
Publikováno v:
Reproductive Biology and Endocrinology, Vol 22, Iss 1, Pp 1-8 (2024)
Abstract Context Acromegaly is a rare disease caused by excessive growth hormone (GH) secretion, mostly induced by pituitary adenomas. The care of pregnant women with acromegaly is challenging, in part due to existing clinical data being limited and
Externí odkaz:
https://doaj.org/article/91dde4d6e61c417a9b4449784289f2ea
Publikováno v:
Biogeosciences, Vol 19, Pp 1067-1085 (2022)
Global emissions linked to wastewater treatment are estimated to account for up to 1.5 % of total greenhouse gas (GHG) emissions globally. However, few studies have measured GHG emissions from domestic on-site treatment systems (DWWTSs) directly. In
Externí odkaz:
https://doaj.org/article/c717e2897eb8406081e8833996d0bc76
Publikováno v:
Free Neuropathology, Vol 2 (2021)
Atypical teratoid/rhabdoid tumors (AT/RT) are aggressively growing malignant embryonal neoplasms of the central nervous system (CNS), which mainly affect young children. Loss of SMARCB1/INI1 (or SMARCA4 in rare cases) is recognized as the genetic hal
Externí odkaz:
https://doaj.org/article/ae1c59f0c1f44a5ea5a906728ae73bd0
Autor:
Markus Glatzel, Wolfgang Saeger, Jannik von Schöning, Ulrich J. Knappe, Dieter K. Lüdecke, Michael Buchfelder, Rof Buslei, Jörg Flitsch, Rundolph Fahlbusch, Jochen Herms, Walter J. Schulz-Schaeffer, Markus Bergmann
Publikováno v:
Hormones. 21:653-663
Purpose/Objective Multiple tumorous lesions in one pituitary gland are rare and mostly described in case reports. Their incidences and combinations are defined in larger collectives. Therefore, we analyzed our large collection for double tumors and c
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Autor:
Michael Buchfelder, Thomas Rüdiger, Rolf Buslei, Christian Hagel, Jochen Herms, Udo Kellner, Jörg Flitsch, Ulrich J. Knappe, Markus Bergmann, Wolfgang Saeger, Ulrich Schüller
Publikováno v:
Pituitary
Pituitary 24(6), 904-913 (2021). doi:10.1007/s11102-021-01164-1
Pituitary 24(6), 904-913 (2021). doi:10.1007/s11102-021-01164-1
Purpose Pituitary adenoma (PA) constitutes the third most common intracranial neoplasm. The mostly benign endocrine lesions express no hormone (null cell PA) or the pituitary hormone(s) of the cell lineage of origin. In 0.5–1.5% of surgical specime
Publikováno v:
Water Research. 236:119968
Autor:
Beate Ditzen, Wolfgang Saeger, Manuel Schmidt, Martin Fassnacht, Werner Paulus, C. Jaursch-Hancke, Ulrich J. Knappe, Rüdiger Gerlach, Elfriede Gertzen, Jörg Flitsch, Martin Reincke, Timo Deutschbein, Jürgen Honegger, Jörg Bojunga, Gerhard A. Horstmann, Arend Koch, Ilonka Kreitschmann-Andermahr, Mirjam Kunz, Helmut Wilhelm, Wolf A. Lagrèze, Michael Buchfelder, Matthias M. Weber, Nils H. Nicolay
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 129:250-264
Although non-functioning pituitary tumors are frequent, diagnostic and therapeutic concepts are not well standardized. We here present the first German multidisciplinary guideline on this topic. The single most important message is to manage the pati
Publikováno v:
Journal of Neurological Surgery Part A: Central European Neurosurgery. 82:034-042
Background The long-term outcome of facet joint replacement (FJR) still is to be proven. Methods We present a prospective case series of 26 (male-to-female ratio of 1:1; mean age: 61 years) patients undergoing FJR with a follow-up of at least 1 year
Publikováno v:
European Journal of Endocrinology. 182:275-284
Background If biochemical control of acromegaly is not achieved by operation and medication, radiotherapy may be indicated. Objective To describe fractionated radiotherapy (FRT) and stereotactic radiosurgery (SRS) regarding excess of IGF-1 and pituit