نتایج جستجو برای: hipple lindau

تعداد نتایج: 2632  

2008
Na Ayudhya Peter G. Waterman Gloria Karagianis

Santi Sakdarat1*, Aussavashai Shuyprom2, Thaweephol Dechatiwongse Na Ayudhya2, Peter G. Waterman3, Gloria Karagianis3 1 School of Chemistry, Institute of Science, Suranaree University of Technology, Nakhon Ratchasima, Thailand 2 Medicinal Plant Research Institute, Department of Medical Science, Ministry of Public Health, Nonthaburi, Thailand 3 Centre for Phytochemistry, Southern Cross Universit...

Journal: :Galicia Clínica 2016

2006

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Journal: :Journal of the National Cancer Institute 1998
K M Egan E Giovannucci

lar genetic mechanisms. Nephrol Dial Transplant 1996;11 Suppl 6:34–7. (10) Thoenes W, Storkel S, Rumpelt HJ, Moll R. Cytomorphological typing of renal cell carcinoma—a new approach. Eur Urol 1990;18 (Suppl 2):6–9. (11) Gnarra JR, Duan DR, Weng Y, Humphrey JS, Chen DY, Lee S, et al. Molecular cloning of the von Hippel–Lindau tumor suppressor gene and its role in renal carcinoma. Biochim Biophys ...

Journal: :Haematologica 2012
Charline Ladroue David Hoogewijs Sophie Gad Romain Carcenac Federica Storti Michel Barrois Anne-Paule Gimenez-Roqueplo Michel Leporrier Nicole Casadevall Olivier Hermine Jean-Jacques Kiladjian André Baruchel Fadi Fakhoury Brigitte Bressac-de Paillerets Jean Feunteun Nathalie Mazure Jacques Pouysségur Roland H Wenger Stéphane Richard Betty Gardie

BACKGROUND Congenital secondary erythrocytoses are due to deregulation of hypoxia inducible factor resulting in overproduction of erythropoietin. The most common germline mutation identified in the hypoxia signaling pathway is the Arginine 200-Tryptophan mutant of the von Hippel-Lindau tumor suppressor gene, resulting in Chuvash polycythemia. This mutant displays a weak deficiency in hypoxia in...

2017
Shimpei Maeda Fuyuhiko Motoi Shuhei Oana Kyohei Ariake Masamichi Mizuma Takanori Morikawa Hiroki Hayashi Kei Nakagawa Takashi Kamei Takeshi Naitoh Michiaki Unno

BACKGROUND von Hippel-Lindau disease is a dominantly inherited multi-system syndrome with neoplastic hallmarks. Pancreatic lesions associated with von Hippel-Lindau include serous cystic neoplasms, simple cysts, and neuroendocrine tumors. The combination of pancreatic neuroendocrine tumors and serous cystic neoplasms is relatively rare, and the surgical treatment of these lesions must consider ...

2015
Joshua Berlin Abdou Abdel-Rehim Constantia Alexandrou Mattia Dalla Brida Mario Gravina Marc Wagner

1Goethe-Universität Frankfurt am Main, Institut für theoretische Physik, Max-von-Laue-Straße 1, D-60438 Frankfurt am Main, Germany 2Computation-based Science and Technology Research Center, The Cyprus Institute, 20 Kavafi Street, 2121 Nicosia, Cyprus 3Department of Physics, University of Cyprus, P.O. Box 20537, 1678 Nicosia, Cyprus 4NIC, DESY, Platanenallee 6, 15738 Zeuthen, Germany 5Università...

Journal: :European urology 2000
C Radmayr H Neumann G Bartsch R Elsner G Janetschek

OBJECTIVES In adults, increasing numbers of adrenalectomies for pheochromocytomas are performed laparoscopically. We report for the first time laparoscopic bilateral subtotal adrenalectomy for pheochromocytomas in an 8-year-old boy with von Hippel-Lindau disease. METHODS In July 1998, an 8-year-old boy with von Hippel-Lindau disease underwent laparoscopic adrenal-sparing surgery for bilateral...

2017
Lone Sunde Eric Jonasch

Von Hippel Lindau is an inherited disease which leads to tumor growth, including hemangioblastomas in the central nervous system and retina. No pharmacological treatment has demonstrated efficacy. Propranolol is a beta-blocker widely used in some neurological and cardiac diseases, and its safety is known. We present a patient diagnosed with Von Hippel Lindau disease who was treated with propran...

Journal: :Current Genetic Medicine Reports 2019

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