Familial Cancer

Pheochromocytoma – where are we? Where should we go? A medical and scientific odyssey

Hartmut P. H. Neumann, Giuseppe Opocher, Andrzej Januszewicz, Charis Eng

Molecular pathogenesis of MEN2-associated tumors

Christian A. Koch

SDHC mutations in hereditary paraganglioma/pheochromocytoma

Ulrich Müller, Christian Troidl, Stephan Niemann

Pheochromocytoma in von Hippel–Lindau disease and neurofibromatosis type 1

Giuseppe Opocher, Pierantonio Conton, Francesca Schiavi, Beatrice Macino, Franco Mantero

Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx

O. Gimm

Multiple endocrine neoplasia type 2

Mariola Peczkowska, Andrzej Januszewicz

Central nervous system manifestations in VHL: genetics, pathology and clinical phenotypic features

Sven Gläsker

Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications

Klaus-Martin Kreusel

Mutations of the SDHB and SDHD genes

Christian Pawlu, Birke Bausch, Hartmut P. H. Neumann

Paragangliomas of the head and neck: diagnosis and treatment

C. C. Boedeker, G. J. Ridder, J. Schipper

Imaging of pheochromocytoma and paraganglioma

I. Brink, S. Hoegerle, J. Klisch, T. A. Bley

Instructions for Authors