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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Oct 12, 2024. (Total: 232444Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: von Hippel-Lindau Disease and SDHD[original query]
Germ-line mutations in nonsyndromic pheochromocytoma.
The New England journal of medicine 2002 May 346 (19): 1459-66.
Neumann Hartmut P H, Bausch Birke, McWhinney Sarah R, Bender Bernhard U, Gimm Oliver, Franke Gerlind, Schipper Joerg, Klisch Joachim, Altehoefer Carsten, Zerres Klaus, Januszewicz Andrzej, Eng Charis, Smith Wendy M, Munk Robin, Manz Tanja, Glaesker Sven, Apel Thomas W, Treier Markus, Reineke Martin, Walz Martin K, Hoang-Vu Cuong, Brauckhoff Michael, Klein-Franke Andreas, Klose Peter, Schmidt Heinrich, Maier-Woelfle Margarete, Peçzkowska Mariola, Szmigielski Cesary, Eng Charis,
Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma.
Endocrine-related cancer 2007 Jun 14 (2): 453-62.
Korpershoek Esther, Petri Bart-Jeroen, van Nederveen Francien H, Dinjens Winand N M, Verhofstad Albert A, de Herder Wouter W, Schmid Sonja, Perren Aurel, Komminoth Paul, de Krijger Ronald
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.
The Lancet. Oncology 2009 Aug 10 (8): 764-71.
van Nederveen Francien H, Gaal José, Favier Judith, Korpershoek Esther, Oldenburg Rogier A, de Bruyn Elly M C A, Sleddens Hein F B M, Derkx Pieter, Rivière Julie, Dannenberg Hilde, Petri Bart-Jeroen, Komminoth Paul, Pacak Karel, Hop Wim C J, Pollard Patrick J, Mannelli Massimo, Bayley Jean-Pierre, Perren Aurel, Niemann Stephan, Verhofstad Albert A, de Bruïne Adriaan P, Maher Eamonn R, Tissier Frédérique, Méatchi Tchao, Badoual Cécile, Bertherat Jérôme, Amar Laurence, Alataki Despoina, Van Marck Eric, Ferrau Francesco, François Jerney, de Herder Wouter W, Peeters Mark-Paul F M Vrancken, van Linge Anne, Lenders Jacques W M, Gimenez-Roqueplo Anne-Paule, de Krijger Ronald R, Dinjens Winand N
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
The Journal of clinical endocrinology and metabolism 2009 Jun 94 (6): 1938-44.
Boedeker Carsten C, Erlic Zoran, Richard Stéphane, Kontny Udo, Gimenez-Roqueplo Anne-Paule, Cascon Alberto, Robledo Mercedes, de Campos José M, van Nederveen Francien H, de Krijger Ronald R, Burnichon Nelly, Gaal José, Walter Martin A, Reschke Kirsten, Wiech Thorsten, Weber Johannes, Rückauer Klaus, Plouin Pierre Francois, Darrouzet Vincent, Giraud Sophie, Eng Charis, Neumann Hartmut P
Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.
The Journal of surgical research 2009 Nov 157 (1): 55-62.
Meyer-Rochow Goswin Y, Smith Janine M, Richardson Anne-Louise, Marsh Deborah J, Sidhu Stan B, Robinson Bruce G, Benn Diana
Isocitrate dehydrogenase mutations are rare in pheochromocytomas and paragangliomas.
The Journal of clinical endocrinology and metabolism 2010 Mar 95 (3): 1274-8.
Gaal José, Burnichon Nelly, Korpershoek Esther, Roncelin Isabelle, Bertherat Jérôme, Plouin Pierre-François, de Krijger Ronald R, Gimenez-Roqueplo Anne-Paule, Dinjens Winand N
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