-
1
-
-
0037046659
-
Germ-line mutations in nonsyndromic pheochromocytomas
-
NEUMANN, H.P.H. et al. 2002. Germ-line mutations in nonsyndromic pheochromocytomas. N. Engl. J. Med. 19: 1459-1466.
-
(2002)
N. Engl. J. Med.
, vol.19
, pp. 1459-1466
-
-
Neumann, H.P.H.1
-
2
-
-
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
-
3
-
-
10744221056
-
Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility
-
ASTUTI, D. et al. 2003. Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility. Clin. Endocrinol. 59: 728-733.
-
(2003)
Clin. Endocrinol.
, vol.59
, pp. 728-733
-
-
Astuti, D.1
-
4
-
-
18344381765
-
Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
-
BAYSAL, B.E. et al. 2002. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. J. Med. Genet. 39: 178-183.
-
(2002)
J. Med. Genet.
, vol.39
, pp. 178-183
-
-
Baysal, B.E.1
-
5
-
-
0035992265
-
Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paragan-glioma
-
DANNENBERG, H. et al. 2002. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paragan-glioma. Clin. Cancer Res. 8: 2061-2066.
-
(2002)
Clin. Cancer Res.
, vol.8
, pp. 2061-2066
-
-
Dannenberg, H.1
-
6
-
-
19944431652
-
Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas
-
VAN HOUTUM, W.H. et al. 2005. Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas. Eur. J. Endocrinol. 152: 87-94.
-
(2005)
Eur. J. Endocrinol.
, vol.152
, pp. 87-94
-
-
Van Houtum, W.H.1
-
7
-
-
0141704510
-
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant pheochromocytomas
-
GIMENEZ-ROQUEPLO, A. et al. 2003. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant pheochromocytomas. Cancer Res. 63: 5615-5621.
-
(2003)
Cancer Res.
, vol.63
, pp. 5615-5621
-
-
Gimenez-Roqueplo, A.1
-
8
-
-
10744224914
-
A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas
-
MAIER-WOELFLE, M. et al. 2004. A novel succinate dehydrogenase subunit B gene mutation, H132P, causes familial malignant sympathetic extraadrenal paragangliomas. J. Clin. Endocrinol. Metab. 89: 362-367.
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 362-367
-
-
Maier-Woelfle, M.1
-
9
-
-
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
-
10
-
-
77955594623
-
A HIF1 alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas
-
Epub July 25
-
DAHIA, P.L. et al. 2005. A HIF1 alpha regulatory loop links hypoxia and mitochondrial signals in pheochromocytomas. PLoS Genet. Epub July 25.
-
(2005)
PLoS Genet.
-
-
Dahia, P.L.1
-
11
-
-
0034671551
-
Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
-
GIMM, O. et al. 2000. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res. 60: 6822-6825.
-
(2000)
Cancer Res.
, vol.60
, pp. 6822-6825
-
-
Gimm, O.1
-
12
-
-
6344223707
-
K40E: A novel succinate dehydrogenase (SDH)B mutation causing familial pheochromocytoma and paraganglioma
-
MCDONNELL, C.M. et al. 2004. K40E: a novel succinate dehydrogenase (SDH)B mutation causing familial pheochromocytoma and paraganglioma. Clin. Endocrinol. 61: 510-514.
-
(2004)
Clin. Endocrinol.
, vol.61
, pp. 510-514
-
-
McDonnell, C.M.1
-
13
-
-
0037422207
-
Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
-
BENN, D.E. et al. 2003. Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Oncogene 22: 1358-1364.
-
(2003)
Oncogene
, vol.22
, pp. 1358-1364
-
-
Benn, D.E.1
-
14
-
-
0034964421
-
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibilty to familial pheochromocytoma and familial paraganglioma
-
ASTUTI, D. et al. 2001. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibilty to familial pheochromocytoma and familial paraganglioma. Am. J. Hum. Genet. 69: 49-54.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 49-54
-
-
Astuti, D.1
-
15
-
-
0036731623
-
Familial malignant cathecholamine-secreting paraganglioa with prolonged survival associated with mutation in the succinate dehydrogenase B gene
-
YOUNG, A.L. et al. 2002. Familial malignant cathecholamine-secreting paraganglioa with prolonged survival associated with mutation in the succinate dehydrogenase B gene. J. Clin. Endocrinol. Metab. 87: 4101-4105.
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 4101-4105
-
-
Young, A.L.1
-
16
-
-
8744288709
-
Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma
-
MCWHINNEY, S.R. et al. 2004. Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma. J. Clin. Endocrinol. Metab. 89: 5694-5699.
-
(2004)
J. Clin. Endocrinol. Metab.
, vol.89
, pp. 5694-5699
-
-
McWhinney, S.R.1
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