Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Kohler, Katrin"'
Publikováno v:
Addiction Biology. Jul99, Vol. 4 Issue 3, p337. 8p. 1 Black and White Photograph, 1 Chart, 1 Graph.
Publikováno v:
21st SIGSPATIAL International Conference on Advances in Geographic Information Systems; 11/6/2018, p10-15, 6p
Autor:
Kohler, Katrin, Al Masri, Ali, Jarausch, Wolfgang, Knauer, Uwe, Höhn, Jukka, Sahib, Layth, Khan, Abidur
Publikováno v:
Julius-Kühn-Archiv; 2021, Issue 467, p553-554, 2p
Autor:
Kohler, Katrin, Roesky, Herbert W.
Publikováno v:
Inorganic Chemistry; 3/27/96, Vol. 35 Issue 7, p1773, 5p, 7 Diagrams, 1 Chart
Autor:
Janssen, Maurits D., Kohler, Katrin
Publikováno v:
Journal of the American Chemical Society. 5/22/96, Vol. 118 Issue 20, p4817. 13p. 8 Diagrams, 7 Charts.
Autor:
Barisson Villares Fragoso, Maria Candida, Vasco de Albuquerque Albuquerque, Edoarda, de Almeida Cardoso, Ana Luiza, Lopes da Rosa, Paula Waki, Bomeny de Paulo, Rodrigo, Massola Schimizu, Maria Heloisa, Seguro, Antonio Carlos, Passarelli, Marisa, Köhler, Katrin, Hübner, Angela, Almeida, Madson Q., Latronico, Ana Claudia, Prado Arnhold, Ivo Jorge, Bilharinho Mendonca, Berenice
Introduction: Triple A syndrome (AAAS) is a rare autosomal recessive disorder characterized by alacrima, achalasia, ACTH-resistant adrenal insufficiency, autonomic dysfunction, and progressive neurodegeneration. Increased oxidative stress, demonstrat
Externí odkaz:
https://tud.qucosa.de/id/qucosa%3A70616
https://tud.qucosa.de/api/qucosa%3A70616/attachment/ATT-0/
https://tud.qucosa.de/api/qucosa%3A70616/attachment/ATT-0/
Autor:
Köhler, Katrin, Schätzl, Robert
Publikováno v:
Julius-Kühn-Archiv, Iss 444, Pp 191-197 (2014)
The western corn rootworm (Diabrotica virgifera virgifera LeConte), holding a quarantine status in the European Union, was first discovered in 2007 in southern Bavaria. In the course of Diabrotica Research Program of Germany and the states of Bavaria
Externí odkaz:
https://doaj.org/article/1bba27e68ce14b61b6b761cff6da4f67
Autor:
Mazur, Artur, Köhler, Katrin, Schülke, Markus, Skunde, Mandy, Ostański, Mariusz, Hübner, Angela
Publikováno v:
Horm Res 2008;69:363–368, ISSN: 0301-0163
Objective: Description of the clinical, biochemical and genetic features of a Polish patient with familial glucocorticoid deficiency. Methods: Detailed clinical investigation, hormonal analysis and sequencing of the coding region of the melanocortin
Externí odkaz:
https://tud.qucosa.de/id/qucosa%3A27575
https://tud.qucosa.de/api/qucosa%3A27575/attachment/ATT-0/
https://tud.qucosa.de/api/qucosa%3A27575/attachment/ATT-0/
Autor:
Salmaggi, Andrea, Zirilli, Lucia, Pantaleoni, Chiara, De Joanna, Gabriella, Del Sorbo, Francesca, Köhler, Katrin, Krumbholz, Manuela, Hübner, Angela, Rochira, Vincenzo
Publikováno v:
Horm Res 2008;70:364–372, ISSN: 0301-0163
Background/Aims: A 33-year-old man was referred for the first time to the Division of Neurology because of the presence and progression of neurological symptoms. Dysphagia, weakness, reduced tear production, and nasal speech were present. In order to
Externí odkaz:
https://tud.qucosa.de/id/qucosa%3A27573
https://tud.qucosa.de/api/qucosa%3A27573/attachment/ATT-0/
https://tud.qucosa.de/api/qucosa%3A27573/attachment/ATT-0/
Autor:
Hedrich, Christian Michael, Zachurzok-Buczynska, Agnieszka, Gawlik, Aneta, Russ, Susanne, Hahn, Gabriele, Köhler, Katrin, Malecka-Tendera, Ewa, Hübner, Angela
Publikováno v:
Horm Res 2009;71:111–119, ISSN: 0301-0163
Background: Autosomal dominant familial neurohypophyseal diabetes insipidus (adFNDI) is a rare disease with symptoms of polydipsia, polyuria and dehydration caused by arginine vasopressin deficiency. Disease onset is within infancy or adolescence. A
Externí odkaz:
https://tud.qucosa.de/id/qucosa%3A27572
https://tud.qucosa.de/api/qucosa%3A27572/attachment/ATT-0/
https://tud.qucosa.de/api/qucosa%3A27572/attachment/ATT-0/