-
1
-
-
23844520735
-
Phaeochromocytoma
-
LENDERS, J.W. et al. 2005. Phaeochromocytoma. Lancet 366: 665-675.
-
(2005)
Lancet
, vol.366
, pp. 665-675
-
-
Lenders, J.W.1
-
2
-
-
0042913365
-
Pheochromocytoma: The expanding genetic differential diagnosis
-
BRYANT, J. et al. 2003. Pheochromocytoma: the expanding genetic differential diagnosis. J. Natl. Cancer. Inst. 95: 1196-1204.
-
(2003)
J. Natl. Cancer. Inst.
, vol.95
, pp. 1196-1204
-
-
Bryant, J.1
-
3
-
-
0036798174
-
The pressure rises: Update on the genetics of phaeochromocytoma
-
MAHER, E.R. & C. ENG. 2002. The pressure rises: update on the genetics of phaeochromocytoma. Hum. Mol. Genet. 11: 2347-2354.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2347-2354
-
-
Maher, E.R.1
Eng, C.2
-
4
-
-
0029836333
-
The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease
-
Seminars in medicine of the Beth Israel Hospital, Boston
-
ENG, C. 1996. Seminars in medicine of the Beth Israel Hospital, Boston. The RET proto-oncogene in multiple endocrine neoplasia type 2 and Hirschsprung's disease. N. Engl. J. Med. 335: 943-951.
-
(1996)
N. Engl. J. Med.
, vol.335
, pp. 943-951
-
-
Eng, C.1
-
5
-
-
0036118172
-
How many pathways to pheochromocytoma?
-
NEUMANN, H.P. et al. 2002. How many pathways to pheochromocytoma? Semin. Nephrol. 22: 89-99.
-
(2002)
Semin. Nephrol.
, vol.22
, pp. 89-99
-
-
Neumann, H.P.1
-
6
-
-
19944424474
-
Multiple endocrine neoplasia type 2
-
PECZKOWSKA, M. & A. JANUSZEWICZ. 2005. Multiple endocrine neoplasia type 2. Fam. Cancer 4: 25-36.
-
(2005)
Fam. Cancer
, vol.4
, pp. 25-36
-
-
Peczkowska, M.1
Januszewicz, A.2
-
7
-
-
0035688775
-
Multiple endocrine neoplasia
-
THAKKER, R.V. 2001. Multiple endocrine neoplasia. Horm Res. 56(Suppl 1): 67-72.
-
(2001)
Horm Res.
, vol.56
, Issue.SUPPL. 1
, pp. 67-72
-
-
Thakker, R.V.1
-
8
-
-
19944425515
-
Pheochromocytoma-associated syndromes: Genes, proteins and functions of RET, VHL and SDHx
-
GIMM, O. 2005. Pheochromocytoma-associated syndromes: genes, proteins and functions of RET, VHL and SDHx. Fam. Cancer 4: 17-23.
-
(2005)
Fam. Cancer
, vol.4
, pp. 17-23
-
-
Gimm, O.1
-
9
-
-
16644373473
-
Role of VHL gene mutation in human cancer
-
KIM, W.Y. & W.G. KAELIN. 2004. Role of VHL gene mutation in human cancer. J. Clin. Oncol. 22: 4991-5004.
-
(2004)
J. Clin. Oncol.
, vol.22
, pp. 4991-5004
-
-
Kim, W.Y.1
Kaelin, W.G.2
-
10
-
-
0344305801
-
On the association of succinate dehydrogenase mutations with hereditary paraganglioma
-
BAYSAL, B.E. 2003. On the association of succinate dehydrogenase mutations with hereditary paraganglioma. Trends Endocrinol. Metab. 14: 453-459.
-
(2003)
Trends Endocrinol. Metab.
, vol.14
, pp. 453-459
-
-
Baysal, B.E.1
-
11
-
-
4143105824
-
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
-
NEUMANN, H.P. et al. 2004. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 292: 943-951.
-
(2004)
JAMA
, vol.292
, pp. 943-951
-
-
Neumann, H.P.1
-
12
-
-
19944367296
-
SDHC mutations in hereditary paraganglioma/pheochromocytoma
-
MULLER, U., C. TROIDL & S. NIEMANN. 2005. SDHC mutations in hereditary paraganglioma/pheochromocytoma. Fam. Cancer 4: 9-12.
-
(2005)
Fam. Cancer
, vol.4
, pp. 9-12
-
-
Muller, U.1
Troidl, C.2
Niemann, S.3
-
13
-
-
4444356015
-
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma
-
BAYSAL, B.E. et al. 2004. An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. J. Med. Genet. 41: 703-709.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 703-709
-
-
Baysal, B.E.1
-
14
-
-
0029159804
-
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
-
BOURGERON, T. et al. 1995. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. Nat. Genet. 11: 144-149.
-
(1995)
Nat. Genet.
, vol.11
, pp. 144-149
-
-
Bourgeron, T.1
-
15
-
-
0141704510
-
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas
-
GIMENEZ-ROQUEPLO, A.P. et al. 2003. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res. 63: 5615-5621.
-
(2003)
Cancer Res.
, vol.63
, pp. 5615-5621
-
-
Gimenez-Roqueplo, A.P.1
-
16
-
-
33845499926
-
The occurrence of SDHB gene mutations in pheochromocytomas
-
VAN NEDERVEEN, F.H. et al. 2006. The occurrence of SDHB gene mutations in pheochromocytomas. Ann. N. Y. Acad. Sci. This Volume.
-
(2006)
Ann. N. Y. Acad. Sci.
, vol.THIS VOLUME
-
-
Van Nederveen, F.H.1
-
17
-
-
51249162117
-
Molecular diagnosis of multiple endocrine neoplasia (MEN) in paraffin-embedded specimens
-
KOMMINOTH, P. et al. 1995. Molecular diagnosis of multiple endocrine neoplasia (MEN) in paraffin-embedded specimens. Endocr. Pathol. 6: 267-278.
-
(1995)
Endocr. Pathol.
, vol.6
, pp. 267-278
-
-
Komminoth, P.1
-
18
-
-
3543053366
-
Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas
-
VAN DER HARST, E. et al. 1998. Prognostic value of RET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas. Int. J. Cancer 79: 537-540.
-
(1998)
Int. J. Cancer
, vol.79
, pp. 537-540
-
-
Van Der Harst, E.1
-
19
-
-
0037431550
-
Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas
-
DANNENBERG, H. et al. 2003. Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas. Int. J. Cancer 105: 190-195.
-
(2003)
Int. J. Cancer
, vol.105
, pp. 190-195
-
-
Dannenberg, H.1
-
20
-
-
2642668463
-
Germline mutations in the VHL gene in patients presenting with phaeochromocytomas
-
VAN DER HARST, E. et al. 1998. Germline mutations in the VHL gene in patients presenting with phaeochromocytomas. Int. J. Cancer 77: 337-340.
-
(1998)
Int. J. Cancer
, vol.77
, pp. 337-340
-
-
Van Der Harst, E.1
-
21
-
-
15744369194
-
Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD
-
DANNENBERG, H. et al. 2005. Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD. J. Clin. Oncol. 23: 1894-1901.
-
(2005)
J. Clin. Oncol.
, vol.23
, pp. 1894-1901
-
-
Dannenberg, H.1
-
22
-
-
0028000277
-
Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing
-
KOMMINOTH, P. et al. 1994. Detection of RET proto-oncogene point mutations in paraffin-embedded pheochromocytoma specimens by nonradioactive single-strand conformation polymorphism analysis and direct sequencing. Am. J. Pathol. 145: 922-929.
-
(1994)
Am. J. Pathol.
, vol.145
, pp. 922-929
-
-
Komminoth, P.1
-
23
-
-
0030781576
-
Sporadic pheochromocytomas are rarely associated with germline mutations in the VHL tumor suppressor gene or the ret protooncogene
-
BRAUCH, H. et al. 1991. Sporadic pheochromocytomas are rarely associated with germline mutations in the VHL tumor suppressor gene or the ret protooncogene. J. Clin. Endocrinol. Metab. 82: 4101-4104.
-
(1991)
J. Clin. Endocrinol. Metab.
, vol.82
, pp. 4101-4104
-
-
Brauch, H.1
-
24
-
-
2942576715
-
Genetic and epigenetic profile of sporadic pheochromocytomas
-
CASCON, A. et al. 2004. Genetic and epigenetic profile of sporadic pheochromocytomas. J. Med. Genet. 41: e30.
-
(2004)
J. Med. Genet.
, vol.41
-
-
Cascon, A.1
-
25
-
-
0037046659
-
Germline mutations in nonsyndromic pheochromocytoma
-
NEUMANN, H.P. et al. 2002. Germline mutations in nonsyndromic pheochromocytoma. N. Engl. J. Med. 346: 1459-1466.
-
(2002)
N. Engl. J. Med.
, vol.346
, pp. 1459-1466
-
-
Neumann, H.P.1
-
26
-
-
0034998621
-
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
-
TASCHNER, P.E. et al. 2001. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. Genes Chromosomes Cancer 31: 274-281.
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 274-281
-
-
Taschner, P.E.1
|