An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis

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...

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Pubblicato in:Lancet Oncol
Autori principali: 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 M
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2009
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4718191/
https://ncbi.nlm.nih.gov/pubmed/19576851
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/S1470-2045(09)70164-0
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