-
1
-
-
0034602950
-
Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma
-
Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard III CW, Cornelisse CJ, Devilee P, Devlin B 2000 Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 287:848-851
-
(2000)
Science
, vol.287
, pp. 848-851
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
Lawrence, E.C.4
Myssiorek, D.5
Bosch, A.6
van der Mey, A.7
Taschner, P.E.8
Rubinstein, W.S.9
Myers, E.N.10
Richard III, C.W.11
Cornelisse, C.J.12
Devilee, P.13
Devlin, B.14
-
2
-
-
0033767445
-
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
-
Niemann S, Muller U 2000 Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet 26:268-270
-
(2000)
Nat Genet
, vol.26
, pp. 268-270
-
-
Niemann, S.1
Muller, U.2
-
3
-
-
0034964421
-
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
-
Astuti D, Latif F, Dallol A, Dahia PL, Douglas F, George E, Skoldberg F, Husebye ES, Eng C, Maher ER 2001 Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69:49-54
-
(2001)
Am J Hum Genet
, vol.69
, pp. 49-54
-
-
Astuti, D.1
Latif, F.2
Dallol, A.3
Dahia, P.L.4
Douglas, F.5
George, E.6
Skoldberg, F.7
Husebye, E.S.8
Eng, C.9
Maher, E.R.10
-
4
-
-
0037024507
-
New insights into the genetics of familial chromaffin cell tumors
-
Koch CA, Vortmeyer AO, Zhuang Z, Brouwers FM, Pacak K 2002 New insights into the genetics of familial chromaffin cell tumors. Ann NY Acad Sci 970:11-28
-
(2002)
Ann NY Acad Sci
, vol.970
, pp. 11-28
-
-
Koch, C.A.1
Vortmeyer, A.O.2
Zhuang, Z.3
Brouwers, F.M.4
Pacak, K.5
-
5
-
-
33644822473
-
Clinical presentation and penetrance of pheochromocytoma/ paraganglioma syndromes
-
Benn DE, Gimenez-Roqueplo AP, Reilly JR, Bertherat J, Burgess J, Byth K, Croxson M, Dahia PL, Elston M, Gimm O, Henley D, Herman P, Murday V, Niccoli-Sire P, Pasieka JL, Rohmer V, Tucker K, Jeunemaitre X, Marsh DJ, Plouin PF, Robinson BG 2006 Clinical presentation and penetrance of pheochromocytoma/ paraganglioma syndromes. J Clin Endocrinol Metab 91:827-836
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 827-836
-
-
Benn, D.E.1
Gimenez-Roqueplo, A.P.2
Reilly, J.R.3
Bertherat, J.4
Burgess, J.5
Byth, K.6
Croxson, M.7
Dahia, P.L.8
Elston, M.9
Gimm, O.10
Henley, D.11
Herman, P.12
Murday, V.13
Niccoli-Sire, P.14
Pasieka, J.L.15
Rohmer, V.16
Tucker, K.17
Jeunemaitre, X.18
Marsh, D.J.19
Plouin, P.F.20
Robinson, B.G.21
more..
-
6
-
-
4143105824
-
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations
-
Neumann HP, Pawlu C, Peczkowska M, Bausch B, McWhinney SR, Muresan M, Buchta M, Franke G, Klisch J, Bley TA, Hoegerle S, Boedeker CC, Opocher G, Schipper J, Januszewicz A, Eng C 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
Pawlu, C.2
Peczkowska, M.3
Bausch, B.4
McWhinney, S.R.5
Muresan, M.6
Buchta, M.7
Franke, G.8
Klisch, J.9
Bley, T.A.10
Hoegerle, S.11
Boedeker, C.C.12
Opocher, G.13
Schipper, J.14
Januszewicz, A.15
Eng, C.16
-
7
-
-
33644834491
-
Genetic testing in pheochromocytoma or functional paraganglioma
-
Amar L, Bertherat J, Baudin E, Ajzenberg C, Bressac-de Paillerets B, Chabre O, Chamontin B, Delemer B, Giraud S, Murat A, Niccoli-Sire P, Richard S, Rohmer V, Sadoul JL, Strompf L, Schlumberger M, Bertagna X, Plouin PF, Jeunemaitre X, Gimenez-Roqueplo AP 2005 Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 23:8812-8818
-
(2005)
J Clin Oncol
, vol.23
, pp. 8812-8818
-
-
Amar, L.1
Bertherat, J.2
Baudin, E.3
Ajzenberg, C.4
Bressac-de Paillerets, B.5
Chabre, O.6
Chamontin, B.7
Delemer, B.8
Giraud, S.9
Murat, A.10
Niccoli-Sire, P.11
Richard, S.12
Rohmer, V.13
Sadoul, J.L.14
Strompf, L.15
Schlumberger, M.16
Bertagna, X.17
Plouin, P.F.18
Jeunemaitre, X.19
Gimenez-Roqueplo, A.P.20
more..
-
8
-
-
0036731623
-
Familial malignant catecholamine-secreting paraganglioma with prolonged survival associated with mutation in the succinate dehydrogenase B gene
-
Young AL, Baysal BE, Deb A, Young Jr WF 2002 Familial malignant catecholamine-secreting paraganglioma 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
Baysal, B.E.2
Deb, A.3
Young Jr, W.F.4
-
9
-
-
33751528825
-
High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: Implications for genetic testing
-
Brouwers FM, Eisenhofer G, Tao JJ, Kant JA, Adams KT, Linehan WM, Pacak K 2006 High frequency of SDHB germline mutations in patients with malignant catecholamine-producing paragangliomas: implications for genetic testing. J Clin Endocrinol Metab 91:4505-4509
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 4505-4509
-
-
Brouwers, F.M.1
Eisenhofer, G.2
Tao, J.J.3
Kant, J.A.4
Adams, K.T.5
Linehan, W.M.6
Pacak, K.7
-
10
-
-
0034671551
-
Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
-
Gimm O, Armanios M, Dziema H, Neumann HP, Eng C 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
Armanios, M.2
Dziema, H.3
Neumann, H.P.4
Eng, C.5
-
11
-
-
0035874016
-
Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma
-
Milunsky JM, Maher TA, Michels VV, Milunsky A 2001 Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma. Am J Med Genet 100:311-314
-
(2001)
Am J Med Genet
, vol.100
, pp. 311-314
-
-
Milunsky, J.M.1
Maher, T.A.2
Michels, V.V.3
Milunsky, A.4
-
12
-
-
0042566135
-
Altitude is a phenotypic modifier in hereditary paraganglioma type 1: Evidence for an oxygen-sensing defect
-
Astrom K, Cohen JE, Willett-Brozick JE, Aston CE, Baysal BE 2003 Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect. Hum Genet 113:228-237
-
(2003)
Hum Genet
, vol.113
, pp. 228-237
-
-
Astrom, K.1
Cohen, J.E.2
Willett-Brozick, J.E.3
Aston, C.E.4
Baysal, B.E.5
-
13
-
-
19944431652
-
Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHDlinked head and neck paragangliomas
-
van Houtum WH, Corssmit EP, Douwes Dekker PB, Jansen JC, van der Mey AG, Brocker-Vriends AH, Taschner PE, Losekoot M, Frolich M, Stokkel MP, Cornelisse CJ, Romijn JA 2005 Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHDlinked head and neck paragangliomas. Eur J Endocrinol 152:87-94
-
(2005)
Eur J Endocrinol
, vol.152
, pp. 87-94
-
-
van Houtum, W.H.1
Corssmit, E.P.2
Douwes Dekker, P.B.3
Jansen, J.C.4
van der Mey, A.G.5
Brocker-Vriends, A.H.6
Taschner, P.E.7
Losekoot, M.8
Frolich, M.9
Stokkel, M.P.10
Cornelisse, C.J.11
Romijn, J.A.12
-
14
-
-
0034998621
-
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
-
Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Brocker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P 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
Jansen, J.C.2
Baysal, B.E.3
Bosch, A.4
Rosenberg, E.H.5
Brocker-Vriends, A.H.6
van Der Mey, A.G.7
van Ommen, G.J.8
Cornelisse, C.J.9
Devilee, P.10
-
15
-
-
27244446452
-
Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene
-
Schiavi F, Boedeker CC, Bausch B, Peczkowska M, Gomez CF, Strassburg T, Pawlu C, Buchta M, Salzmann M, Hoffmann MM, Berlis A, Brink I, Cybulla M, Muresan M, Walter MA, Forrer F, Valimaki M, Kawecki A, Szutkowski Z, Schipper J, Walz MK, Pigny P, Bauters C, Willet-Brozick JE, Baysal BE, Januszewicz A, Eng C, Opocher G, Neumann HP 2005 Predictors and prevalence of paraganglioma syndrome associated with mutations of the SDHC gene. JAMA 294:2057-2063
-
(2005)
JAMA
, vol.294
, pp. 2057-2063
-
-
Schiavi, F.1
Boedeker, C.C.2
Bausch, B.3
Peczkowska, M.4
Gomez, C.F.5
Strassburg, T.6
Pawlu, C.7
Buchta, M.8
Salzmann, M.9
Hoffmann, M.M.10
Berlis, A.11
Brink, I.12
Cybulla, M.13
Muresan, M.14
Walter, M.A.15
Forrer, F.16
Valimaki, M.17
Kawecki, A.18
Szutkowski, Z.19
Schipper, J.20
Walz, M.K.21
Pigny, P.22
Bauters, C.23
Willet-Brozick, J.E.24
Baysal, B.E.25
Januszewicz, A.26
Eng, C.27
Opocher, G.28
Neumann, H.P.29
more..
-
16
-
-
34147182966
-
Effects of therapy with [177Lu-DOTA0, Tyr3]octreotate in patients with paraganglioma, meningioma, small cell lung carcinoma, and melanoma
-
van Essen M, Krenning EP, Kooij PP, Bakker WH, Feelders RA, de Herder WW, Wolbers JG, Kwekkeboom DJ 2006 Effects of therapy with [177Lu-DOTA0, Tyr3]octreotate in patients with paraganglioma, meningioma, small cell lung carcinoma, and melanoma. J Nucl Med 47:1599-1606
-
(2006)
J Nucl Med
, vol.47
, pp. 1599-1606
-
-
van Essen, M.1
Krenning, E.P.2
Kooij, P.P.3
Bakker, W.H.4
Feelders, R.A.5
de Herder, W.W.6
Wolbers, J.G.7
Kwekkeboom, D.J.8
-
17
-
-
0035005519
-
Pheochromocytoma
-
Klingler HC, Klingler PJ, Martin Jr JK, Smallridge RC, Smith SL, Hinder RA 2001 Pheochromocytoma. Urology 57:1025-1032
-
(2001)
Urology
, vol.57
, pp. 1025-1032
-
-
Klingler, H.C.1
Klingler, P.J.2
Martin Jr, J.K.3
Smallridge, R.C.4
Smith, S.L.5
Hinder, R.A.6
-
18
-
-
0027134895
-
Comparison of adrenal and extraadrenal pheochromocytomas
-
Pommier RF, Vetto JT, Billingsly K, Woltering EA, Brennan MF 1993 Comparison of adrenal and extraadrenal pheochromocytomas. Surgery 114:1160-1165
-
(1993)
Surgery
, vol.114
, pp. 1160-1165
-
-
Pommier, R.F.1
Vetto, J.T.2
Billingsly, K.3
Woltering, E.A.4
Brennan, M.F.5
-
19
-
-
2142853586
-
Hypotension in a woman with a metastatic dopamine-secreting carotid body tumor
-
Koch CA, Rodbard JS, Brouwers FM, Eisenhofer G, Pacak K 2003 Hypotension in a woman with a metastatic dopamine-secreting carotid body tumor. Endocr Pract 9:310-314
-
(2003)
Endocr Pract
, vol.9
, pp. 310-314
-
-
Koch, C.A.1
Rodbard, J.S.2
Brouwers, F.M.3
Eisenhofer, G.4
Pacak, K.5
|