2009The Lancet OncologyOpen access

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

Francien H. van Nederveen, José Gaal, Judith Favier, Esther Korpershoek, Rogier A. Oldenburg, Elly MCA de Bruyn, Hein F.B.M. Sleddens, Pieter Derkx, Julie Rivière, Hilde Dannenberg, Bart‐Jeroen Petri, Paul Komminoth, Karel Pacák, Wim C.J. Hop, Patrick J. Pollard, Massimo Mannelli, Jean‐Pierre Bayley, Aurel Perren, Stephan Niemann, A.A.J. Verhofstad, Adriaan P. de Bruı̈ne, Eamonn R. Maher, Frédérique Tissier, Tchao Méatchi, Cécile Badoual, Jérôme Bertherat, Laurence Amar, Despoina Alataki, Eric Van Marck, Francesco Ferraù, Jerney François, Wouter W. de Herder, Mark-Paul FM Vrancken Peeters, Anne van Linge, Jacques W.M. Lenders, Anne‐Paule Gimenez‐Roqueplo, Ronald R. de Krijger, Winand N.M. Dinjens

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Key concepts: SDHB, SDHD, Paraganglioma, Pheochromocytoma, SDHA, Medicine, Germline mutation, Pathology

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