nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Author Index
|
|
|
2005 |
4 |
1 |
p. 141-147 |
artikel |
2 |
Central nervous system manifestations in VHL: genetics, pathology and clinical phenotypic features
|
Gläsker, Sven |
|
2005 |
4 |
1 |
p. 37-42 |
artikel |
3 |
History of the International Collaborative Group on Hereditary NonPolyposis Colorectal Cancer
|
Lynch, Henry T. |
|
2005 |
4 |
1 |
p. 3-5 |
artikel |
4 |
Imaging of pheochromocytoma and paraganglioma
|
Brink, I. |
|
2005 |
4 |
1 |
p. 61-68 |
artikel |
5 |
Instructions for Authors
|
|
|
2005 |
4 |
1 |
p. 69-71 |
artikel |
6 |
Molecular pathogenesis of MEN2-associated tumors
|
Koch, Christian A. |
|
2005 |
4 |
1 |
p. 3-7 |
artikel |
7 |
Multiple endocrine neoplasia type 2
|
Peczkowska, Mariola |
|
2005 |
4 |
1 |
p. 25-36 |
artikel |
8 |
Mutations of the SDHB and SDHD genes
|
Pawlu, Christian |
|
2005 |
4 |
1 |
p. 49-54 |
artikel |
9 |
Ophthalmological manifestations in VHL and NF 1: pathological and diagnostic implications
|
Kreusel, Klaus-Martin |
|
2005 |
4 |
1 |
p. 43-47 |
artikel |
10 |
Origins of the Leeds Castle Polyposis Group
|
Neale, Kay |
|
2005 |
4 |
1 |
p. 1-2 |
artikel |
11 |
Paragangliomas of the head and neck: diagnosis and treatment
|
Boedeker, C. C. |
|
2005 |
4 |
1 |
p. 55-59 |
artikel |
12 |
Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx
|
Gimm, O. |
|
2005 |
4 |
1 |
p. 17-23 |
artikel |
13 |
Pheochromocytoma in von Hippel–Lindau disease and neurofibromatosis type 1
|
Opocher, Giuseppe |
|
2005 |
4 |
1 |
p. 13-16 |
artikel |
14 |
Pheochromocytoma – where are we? Where should we go? A medical and scientific odyssey
|
Neumann, Hartmut P. H. |
|
2005 |
4 |
1 |
p. 1 |
artikel |
15 |
Programme
|
|
|
2005 |
4 |
1 |
p. 7-140 |
artikel |
16 |
SDHC mutations in hereditary paraganglioma/pheochromocytoma
|
Müller, Ulrich |
|
2005 |
4 |
1 |
p. 9-12 |
artikel |