| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
Author Index
|
|
|
2005
|
4 |
1 |
p. 141-147
|
article
|
| 2 |
Central nervous system manifestations in VHL: genetics, pathology and clinical phenotypic features
|
Gläsker, Sven
|
|
2005
|
4 |
1 |
p. 37-42
|
article
|
| 3 |
History of the International Collaborative Group on Hereditary NonPolyposis Colorectal Cancer
|
Lynch, Henry T.
|
|
2005
|
4 |
1 |
p. 3-5
|
article
|
| 4 |
Imaging of pheochromocytoma and paraganglioma
|
Brink, I.
|
|
2005
|
4 |
1 |
p. 61-68
|
article
|
| 5 |
Instructions for Authors
|
|
|
2005
|
4 |
1 |
p. 69-71
|
article
|
| 6 |
Molecular pathogenesis of MEN2-associated tumors
|
Koch, Christian A.
|
|
2005
|
4 |
1 |
p. 3-7
|
article
|
| 7 |
Multiple endocrine neoplasia type 2
|
Peczkowska, Mariola
|
|
2005
|
4 |
1 |
p. 25-36
|
article
|
| 8 |
Mutations of the SDHB and SDHD genes
|
Pawlu, Christian
|
|
2005
|
4 |
1 |
p. 49-54
|
article
|
| 9 |
Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications
|
Kreusel, Klaus-Martin
|
|
2005
|
4 |
1 |
p. 43-47
|
article
|
| 10 |
Origins of the Leeds Castle Polyposis Group
|
Neale, Kay
|
|
2005
|
4 |
1 |
p. 1-2
|
article
|
| 11 |
Paragangliomas of the head and neck: diagnosis and treatment
|
Boedeker, C. C.
|
|
2005
|
4 |
1 |
p. 55-59
|
article
|
| 12 |
Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx
|
Gimm, O.
|
|
2005
|
4 |
1 |
p. 17-23
|
article
|
| 13 |
Pheochromocytoma in von Hippel–Lindau disease and neurofibromatosis type 1
|
Opocher, Giuseppe
|
|
2005
|
4 |
1 |
p. 13-16
|
article
|
| 14 |
Pheochromocytoma – where are we? Where should we go? A medical and scientific odyssey
|
Neumann, Hartmut P. H.
|
|
2005
|
4 |
1 |
p. 1
|
article
|
| 15 |
Programme
|
|
|
2005
|
4 |
1 |
p. 7-140
|
article
|
| 16 |
SDHC mutations in hereditary paraganglioma/pheochromocytoma
|
Müller, Ulrich
|
|
2005
|
4 |
1 |
p. 9-12
|
article
|
Journal description