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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Detaylı Bibliyografya
Yayımlandı:Lancet Oncol
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2009
Konular:
Article
Online Erişim: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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