-
3
-
-
0029159804
-
Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency
-
T Bourgeron P Rustin D. Chretien 1995 Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency Nat Genet 11 144
-
(1995)
Nat Genet
, vol.11
, pp. 144
-
-
Bourgeron, T.1
Rustin, P.2
Chretien, D.3
-
4
-
-
0035213138
-
The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway
-
AP Gimenez-Roqueplo J Favier P. Rustin 2001 The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia pathway Am J Hum Genet 69 1186
-
(2001)
Am J Hum Genet
, vol.69
, pp. 1186
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
5
-
-
0036774422
-
Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma
-
AP Gimenez-Roqueplo J Favier P. Rustin 2002 Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma J Clin Endocrinol Metab 87 4771
-
(2002)
J Clin Endocrinol Metab
, vol.87
, pp. 4771
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
6
-
-
0033587146
-
The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis
-
PH. Maxwell MS Wiesener GW. Chang 1999 The tumour suppressor protein VHL targets hypoxia-inducible factors for oxygen-dependent proteolysis Nature 399 271
-
(1999)
Nature
, vol.399
, pp. 271
-
-
Maxwell, P.H.1
Wiesener, M.S.2
Chang, G.W.3
-
7
-
-
0026849378
-
A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter
-
P Heutink AG van der Mey LA. Sandkuijl 1992 A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter Hum Mol Genet 1 7
-
(1992)
Hum Mol Genet
, vol.1
, pp. 7
-
-
Heutink, P.1
Van Der Mey, A.G.2
Sandkuijl, L.A.3
-
8
-
-
0036712593
-
Hereditary paraganglioma targets diverse paraganglia
-
BE. Baysal 2002 Hereditary paraganglioma targets diverse paraganglia J Med Genet 39 617
-
(2002)
J Med Genet
, vol.39
, pp. 617
-
-
Baysal, B.E.1
-
9
-
-
0141704510
-
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas
-
AP Gimenez-Roqueplo J Favier P. Rustin 2003 Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas Cancer Res 63 5615
-
(2003)
Cancer Res
, vol.63
, pp. 5615
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
-
10
-
-
0037139449
-
Biochemical diagnosis of pheochromocytoma: Which test is best?
-
JW Lenders K Pacak MM. Walther 2002 Biochemical diagnosis of pheochromocytoma: which test is best? JAMA 287 1427
-
(2002)
JAMA
, vol.287
, pp. 1427
-
-
Lenders, J.W.1
Pacak, K.2
Walther, M.M.3
-
11
-
-
0027508442
-
Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease
-
HP Neumann DP Berger G. Sigmund 1993 Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease N Engl J Med 329 1531
-
(1993)
N Engl J Med
, vol.329
, pp. 1531
-
-
Neumann, H.P.1
Berger, D.P.2
Sigmund, G.3
-
12
-
-
0036007324
-
Pheochromocytomas: Detection with 18F DOPA whole body PET-initial results
-
S Hoegerle E Nitzsche C. Altehoefer 2002 Pheochromocytomas: detection with 18F DOPA whole body PET-initial results Radiology 222 507
-
(2002)
Radiology
, vol.222
, pp. 507
-
-
Hoegerle, S.1
Nitzsche, E.2
Altehoefer, C.3
-
13
-
-
0038245162
-
18F-DOPA positron emission tomography for the detection of glomus tumours
-
S Hoegerle N Ghanem C. Altehoefer 2003 18F-DOPA positron emission tomography for the detection of glomus tumours Eur J Nucl Med Mol Imag 30 689
-
(2003)
Eur J Nucl Med Mol Imag
, vol.30
, pp. 689
-
-
Hoegerle, S.1
Ghanem, N.2
Altehoefer, C.3
-
14
-
-
0035528831
-
6-[18F]fluorodopamine positron emission tomographic (PET) scanning for diagnostic localization of pheochromocytoma
-
K Pacak G Eisenhofer JA. Carrasquillo 2001 6-[18F]fluorodopamine positron emission tomographic (PET) scanning for diagnostic localization of pheochromocytoma Hypertension 38 6
-
(2001)
Hypertension
, vol.38
, pp. 6
-
-
Pacak, K.1
Eisenhofer, G.2
Carrasquillo, J.A.3
-
15
-
-
0141733282
-
Superiority of 6-[18F]-fluorodopamine positron emission tomography versus [131I]-metaiodobenzylguanidine scintigraphy in the localization of metastatic pheochromocytoma
-
I Ilias J Yu JA. Carrasquillo 2003 Superiority of 6-[18F]-fluorodopamine positron emission tomography versus [131I]-metaiodobenzylguanidine scintigraphy in the localization of metastatic pheochromocytoma J Clin Endocrinol Metab 88 4083
-
(2003)
J Clin Endocrinol Metab
, vol.88
, pp. 4083
-
-
Ilias, I.1
Yu, J.2
Carrasquillo, J.A.3
-
16
-
-
0037422207
-
Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
-
E Benn D S Croxson M K. Tucker 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
-
(2003)
Oncogene
, vol.22
, pp. 1358
-
-
Benn, D.E.1
Croxson, M.S.2
Tucker, K.3
-
17
-
-
18344381765
-
). Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
-
BE Baysal JE Willett-Brozick EC. Lawrence 2002 ). Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas J Med Genet 39 178
-
(2002)
J Med Genet
, vol.39
, pp. 178
-
-
Baysal, B.E.1
Willett-Brozick, J.E.2
Lawrence, E.C.3
-
18
-
-
0034964421
-
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
-
D Astuti F Latif A. Dallol 2001 Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma Am J Hum Genet 69 49
-
(2001)
Am J Hum Genet
, vol.69
, pp. 49
-
-
Astuti, D.1
Latif, F.2
Dallol, A.3
-
19
-
-
0034999087
-
Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss
-
RF Badenhop S Cherian RS. Lord 2001 Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss Genes Chromosomes Cancer 31 255
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 255
-
-
Badenhop, R.F.1
Cherian, S.2
Lord, R.S.3
-
20
-
-
0034671551
-
Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
-
O Gimm M Armanios H. Dziema 2000 Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma Cancer Res 60 6822
-
(2000)
Cancer Res
, vol.60
, pp. 6822
-
-
Gimm, O.1
Armanios, M.2
Dziema, H.3
-
21
-
-
0034998621
-
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
-
PE Taschner JC Jansen BE. Baysal 2001 Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene Genes Chromosomes Cancer 31 274
-
(2001)
Genes Chromosomes Cancer
, vol.31
, pp. 274
-
-
Taschner, P.E.1
Jansen, J.C.2
Baysal, B.E.3
-
22
-
-
0035857957
-
Germline SDHD mutation in familial phaeochromocytoma
-
D Astuti F Douglas TW. Lennard 2001 Germline SDHD mutation in familial phaeochromocytoma Lancet 357 1181
-
(2001)
Lancet
, vol.357
, pp. 1181
-
-
Astuti, D.1
Douglas, F.2
Lennard, T.W.3
-
23
-
-
0035874016
-
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma
-
JM Milunsky TA Maher VV. Michels 2001 Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma Am J Med Genet 100 311
-
(2001)
Am J Med Genet
, vol.100
, pp. 311
-
-
Milunsky, J.M.1
Maher, T.A.2
Michels, V.V.3
-
24
-
-
0034602950
-
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
-
BE Baysal RE Ferrell JE. Willett-Brozick 2000 Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma Science 287 848
-
(2000)
Science
, vol.287
, pp. 848
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
-
25
-
-
0035991632
-
Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma
-
A Cascon S Ruiz-Llorente A. Cebrian 2002 Identification of novel SDHD mutations in patients with phaeochromocytoma and/or paraganglioma Eur J Hum Genet 10 457
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 457
-
-
Cascon, A.1
Ruiz-Llorente, S.2
Cebrian, A.3
-
26
-
-
0035992265
-
Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma
-
H Dannenberg WN Dinjens M. Abbou 2002 Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma Clin Cancer Res 8 2061
-
(2002)
Clin Cancer Res
, vol.8
, pp. 2061
-
-
Dannenberg, H.1
Dinjens, W.N.2
Abbou, M.3
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