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

   • Hartmut P. H. Neumann
   • Giuseppe Opocher
   • Charis Eng

   OriginalPaper Pages: 1 - 1

2. Molecular pathogenesis of MEN2-associated tumors

   • Christian A. Koch

   Review Pages: 3 - 7

3. SDHC mutations in hereditary paraganglioma/pheochromocytoma

   • Ulrich Müller
   • Christian Troidl
   • Stephan Niemann

   OriginalPaper Pages: 9 - 12

4. Pheochromocytoma in von Hippel–Lindau disease and neurofibromatosis type 1

   • Giuseppe Opocher
   • Pierantonio Conton
   • Franco Mantero

   OriginalPaper Pages: 13 - 16

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

   • O. Gimm

   OriginalPaper Pages: 17 - 23

6. Multiple endocrine neoplasia type 2

   • Mariola Peczkowska
   • Andrzej Januszewicz

   OriginalPaper Pages: 25 - 36

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

   • Sven Gläsker

   Review Pages: 37 - 42

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

   • Klaus-Martin Kreusel

   Review Pages: 43 - 47

9. Mutations of the SDHB and SDHD genes

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

   Review Pages: 49 - 54

10. Paragangliomas of the head and neck: diagnosis and treatment

    • C. C. Boedeker
    • G. J. Ridder
    • J. Schipper

    Review Pages: 55 - 59

11. Imaging of pheochromocytoma and paraganglioma

    • I. Brink
    • S. Hoegerle
    • T. A. Bley

    OriginalPaper Pages: 61 - 68

12. Instructions for Authors

    OriginalPaper Pages: 69 - 71