Zobrazeno 1 - 10 of 88 pro vyhledávání: '"K Dudziak"'
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Diagnostik und Therapie bei funktionell aktiven pankreatischen neuroendokrinen Tumoren
Autor: M Anlauf, Marius Horger, K. Müssig, K Dudziak, P E Goretzki
Publikováno v: DMW - Deutsche Medizinische Wochenschrift. 136:1319-1330
Pancreatic neuroendocrine tumours (PNET) are rare entities with an annual incidence of < 100,000. About 1 - 2 % of pancreatic neoplasias are neuroendocrine tumours. About one third of these tumours secrete biologically active substances that lead to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::48716bee1a2814e5cf595e1633a2a5a8
https://doi.org/10.1055/s-0031-1280554
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3
Association of Somatostatin Receptor 2 Immunohistochemical Expression with [111In]-DTPA Octreotide Scintigraphy and [68Ga]-DOTATOC PET/CT in Neuroendocrine Tumors
Autor: C. Pfannenberg, Karsten Müssig, Stefan Schulz, K. Dudziak, Stephan Petersenn, Baptist Gallwitz, B. Ueberberg, Manfred Wehrmann, HU Häring, Roland Bares, Mö Öksüz, M. Horger
Publikováno v: Hormone and Metabolic Research. 42:599-606
In the absence of preoperative somatostatin receptor ( SST) scans, knowledge of immunohistochemical SST2 tumor expression may help predicting the success of somatostatin analogue-based follow-up studies and treatment of neuroendocrine tumors (NET). W
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aa529c542dfd5976adf6cccd98c932a
https://doi.org/10.1055/s-0030-1253354
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6
Glucose-Raising Genetic Variants in MADD and ADCY5 Impair Conversion of Proinsulin to Insulin
Autor: K Dudziak, Norbert Stefan, Hans-Ulrich Häring, Robert Wagner, Silke A. Herzberg-Schäfer, Fausto Machicao, Andreas Fritsche, Harald Staiger
Publikováno v: PLoS ONE
PLoS ONE, Vol 6, Iss 8, p e23639 (2011)
INTRODUCTION: Recent meta-analyses of genome-wide association studies revealed new genetic loci associated with fasting glycemia. For several of these loci, the mechanism of action in glucose homeostasis is unclear. The objective of the study was to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4864922bf96fbacedeea38f15871184d
http://europepmc.org/articles/PMC3161735
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7
Pituitary carcinoma with malignant growth from first presentation and fulminant clinical course--case report and review of the literature
Autor: Antje Bornemann, Jürgen Honegger, Marius Horger, Karsten Müssig, K Dudziak
Publikováno v: The Journal of clinical endocrinology and metabolism. 96(9)
Although pituitary adenomas are common, pituitary carcinoma is a very rare condition.We report on a 48-yr-old male presenting with pituitary carcinoma with malignant growth from the beginning and a fulminant clinical course and give an overview of th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b84abf4943f858b6698315969c50f4d
https://pubmed.ncbi.nlm.nih.gov/21715538
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8
[Diagnostics and treatment in functional pancreatic neuroendocrine tumours]
Autor: K, Müssig, K, Dudziak, M, Horger, M, Anlauf, P E, Goretzki
Publikováno v: Deutsche medizinische Wochenschrift (1946). 136(24)
Pancreatic neuroendocrine tumours (PNET) are rare entities with an annual incidence of 100,000. About 1 - 2 % of pancreatic neoplasias are neuroendocrine tumours. About one third of these tumours secrete biologically active substances that lead to de
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::81dc63f34832031ca6dd0dfdbedf91fb
https://pubmed.ncbi.nlm.nih.gov/21656454
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