An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with ge...
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC , or SDHD gene mutations: a retrospective and prospective analysis
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Author / Creator
van Nederveen, Francien H, MD , Gaal, José, MD , Favier, Judith, PhD , Korpershoek, Esther, BSc , Oldenburg, Rogier A, MD , de Bruyn, Elly MCA, BSc , Sleddens, Hein FBM, BSc , Derkx, Pieter, BSc , Rivière, Julie, BSc , Dannenberg, Hilde, MD , Petri, Bart-Jeroen, MD , Komminoth, Paul, Prof , Pacak, Karel, Prof , Hop, Wim CJ, PhD , Pollard, Patrick J, MD , Mannelli, Massimo, Prof , Bayley, Jean-Pierre, PhD , Perren, Aurel, MD , Niemann, Stephan, PhD , Verhofstad, Albert A, MD , de Bruïne, Adriaan P, Prof , Maher, Eamonn R, Prof , Tissier, Frédérique, MD , Méatchi, Tchao, MD , Badoual, Cécile, MD , Bertherat, Jérôme, Prof , Amar, Laurence, MD , Alataki, Despoina, MD , Van Marck, Eric, Prof , Ferrau, Francesco, MD , François, Jerney, BSc , de Herder, Wouter W, MD , Peeters, Mark-Paul FM Vrancken, MD , van Linge, Anne, MD , Lenders, Jacques WM, Prof , Gimenez-Roqueplo, Anne-Paule, Prof , de Krijger, Ronald R, MD and Dinjens, Winand NM, Dr
Publisher
England: Elsevier Ltd
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Language
English
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Publisher
England: Elsevier Ltd
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Contents
Summary Background Phaeochromocytomas and paragangliomas are neuro-endocrine tumours that occur sporadically and in several hereditary tumour syndromes, including the phaeochromocytoma–paraganglioma syndrome. This syndrome is caused by germline mutations in succinate dehydrogenase B ( SDHB ), C ( SDHC ), or D ( SDHD ) genes. Clinically, the phaeoch...
Alternative Titles
Full title
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC , or SDHD gene mutations: a retrospective and prospective analysis
Authors, Artists and Contributors
Author / Creator
Gaal, José, MD
Favier, Judith, PhD
Korpershoek, Esther, BSc
Oldenburg, Rogier A, MD
de Bruyn, Elly MCA, BSc
Sleddens, Hein FBM, BSc
Derkx, Pieter, BSc
Rivière, Julie, BSc
Dannenberg, Hilde, MD
Petri, Bart-Jeroen, MD
Komminoth, Paul, Prof
Pacak, Karel, Prof
Hop, Wim CJ, PhD
Pollard, Patrick J, MD
Mannelli, Massimo, Prof
Bayley, Jean-Pierre, PhD
Perren, Aurel, MD
Niemann, Stephan, PhD
Verhofstad, Albert A, MD
de Bruïne, Adriaan P, Prof
Maher, Eamonn R, Prof
Tissier, Frédérique, MD
Méatchi, Tchao, MD
Badoual, Cécile, MD
Bertherat, Jérôme, Prof
Amar, Laurence, MD
Alataki, Despoina, MD
Van Marck, Eric, Prof
Ferrau, Francesco, MD
François, Jerney, BSc
de Herder, Wouter W, MD
Peeters, Mark-Paul FM Vrancken, MD
van Linge, Anne, MD
Lenders, Jacques WM, Prof
Gimenez-Roqueplo, Anne-Paule, Prof
de Krijger, Ronald R, MD
Dinjens, Winand NM, Dr
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4718191
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4718191
Other Identifiers
ISSN
1470-2045
E-ISSN
1474-5488,1470-2045
DOI
10.1016/S1470-2045(09)70164-0
