-
3
-
-
40849088026
-
Paragangliomas of the head and neck
-
DOI 10.1007/s11912-008-0024-9
-
Kupferman ME, Hanna EY,. Paragangliomas of the head and neck. Curr Oncol Rep 2008; 10: 156-161. (Pubitemid 351395476)
-
(2008)
Current Oncology Reports
, vol.10
, Issue.2
, pp. 156-161
-
-
Kupferman, M.E.1
Hanna, E.Y.2
-
4
-
-
68549092484
-
The approach to the patient with paraganglioma
-
Neumann HP, Eng C,. The approach to the patient with paraganglioma. J Clin Endocrinol Metab 2009; 94: 2677-2683.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 2677-2683
-
-
Neumann, H.P.1
Eng, C.2
-
5
-
-
39149143037
-
Pheochromocytoma: An update on genetics and management
-
DOI 10.1677/ERC-07-0142
-
Karagiannis A, Mikhailidis DP, Athyros VG, Harsoulis F,. Pheochromocytoma: an update on genetics and management. Endocr Relat Cancer 2007; 14: 935-956. (Pubitemid 351252428)
-
(2007)
Endocrine-Related Cancer
, vol.14
, Issue.4
, pp. 935-956
-
-
Karagiannis, A.1
Mikhailidis, D.P.2
Athyros, V.G.3
Harsoulis, F.4
-
6
-
-
67650501167
-
Clinical aspects of SDHx-related pheochromocytoma and paraganglioma
-
Timmers HJ, Gimenez-Roqueplo AP, Mannelli M, Pacak K,. Clinical aspects of SDHx-related pheochromocytoma and paraganglioma. Endocr Relat Cancer 2009; 16: 391-400.
-
(2009)
Endocr Relat Cancer
, vol.16
, pp. 391-400
-
-
Timmers, H.J.1
Gimenez-Roqueplo, A.P.2
Mannelli, M.3
Pacak, K.4
-
7
-
-
85036709112
-
-
Pagon R.A. Bird T.D. Dolan C.R. Stephens K. editors. Seattle: University of Washington, Seattle
-
Klein RD, Lloyd RV, Young WF,. Hereditary paraganglioma-pheochromocytoma syndromes. GeneReviews [Internet]. In:, Pagon RA, Bird TD, Dolan CR, Stephens K, editors. Seattle: University of Washington, Seattle; 2009.
-
(2009)
Hereditary Paraganglioma-pheochromocytoma Syndromes. GeneReviews [Internet]
-
-
Klein, R.D.1
Lloyd, R.V.2
Young, W.F.3
-
8
-
-
74049144943
-
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD
-
Ricketts CJ, Forman JR, Rattenberry E, et al. Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD. Hum Mutat 2010; 31: 41-51.
-
(2010)
Hum Mutat
, vol.31
, pp. 41-51
-
-
Ricketts, C.J.1
Forman, J.R.2
Rattenberry, E.3
-
9
-
-
68549092478
-
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas
-
Burnichon N, Rohmer V, Amar L, et al. The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas. J Clin Endocrinol Metab 2009; 94: 2817-2827.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 2817-2827
-
-
Burnichon, N.1
Rohmer, V.2
Amar, L.3
-
10
-
-
77958164441
-
SDHA is a tumor suppressor gene causing paraganglioma
-
Burnichon N, Brière JJ, Libé R, et al. SDHA is a tumor suppressor gene causing paraganglioma. Hum Mol Genet 2010; 19: 3011-3020.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 3011-3020
-
-
Burnichon, N.1
Brière, J.J.2
Libé, R.3
-
11
-
-
33644822473
-
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes
-
DOI 10.1210/jc.2005-1862
-
Benn DE, Gimenez-Roqueplo AP, Reilly JR, et al. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. J Clin Endocrinol Metab 2006; 91: 827-836. (Pubitemid 43357746)
-
(2006)
Journal of Clinical Endocrinology and Metabolism
, vol.91
, Issue.3
, 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.M.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..
-
12
-
-
4143105824
-
Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD and gene mutations
-
DOI 10.1001/jama.292.8.943
-
Neumann HP, Pawlu C, Peczkowska M, et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 2004; 292: 943-951. (Pubitemid 39097204)
-
(2004)
Journal of the American Medical Association
, vol.292
, Issue.8
, pp. 943-951
-
-
Neumann, H.P.H.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
-
13
-
-
0023885121
-
Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference
-
[No authors listed]
-
[No authors listed] Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference. Arch Neurol 1988; 45: 575-578.
-
(1988)
Arch Neurol
, vol.45
, pp. 575-578
-
-
-
14
-
-
34447114512
-
Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1
-
DOI 10.1210/jc.2006-2833
-
Bausch B, Borozdin W, Mautner VF, et al. Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1. J Clin Endocrinol Metab 2007; 92: 2784-2792. (Pubitemid 47037390)
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, Issue.7
, pp. 2784-2792
-
-
Bausch, B.1
Borozdin, W.2
Mautner, V.F.3
Hoffmann, M.M.4
Boehm, D.5
Robledo, M.6
Cascon, A.7
Harenberg, T.8
Schiavi, F.9
Pawlu, C.10
Peczkowska, M.11
Letizia, C.12
Calvieri, S.13
Arnaldi, G.14
Klingenberg-Noftz, R.D.15
Reisch, N.16
Fassina, A.17
Brunaud, L.18
Walter, M.A.19
Mannelli, M.20
MacGregor, G.21
Palazzo, F.F.22
Barontini, M.23
Walz, M.K.24
Kremens, B.25
Brabant, G.26
Pfaffle, R.27
Koschker, A.-C.28
Lohoefner, F.29
Mohaupt, M.30
Gimm, O.31
Jarzab, B.32
McWhinney, S.R.33
Opocher, G.34
Januszewicz, A.35
Kohlhase, J.36
Eng, C.37
Neumann, H.P.H.38
more..
-
15
-
-
0034964421
-
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
-
DOI 10.1086/321282
-
Astuti D, Latif F, Dallol A, et al. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 2001; 69: 49-54. (Pubitemid 32614017)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.1
, pp. 49-54
-
-
Astuti, D.1
Latif, F.2
Dallol, A.3
Dahia, P.L.M.4
Douglas, F.5
George, E.6
Skoldberg, F.7
Husebye, E.S.8
Eng, C.9
Maher, E.R.10
-
16
-
-
33644834491
-
Genetic testing in pheochromocytoma or functional paraganglioma
-
DOI 10.1200/JCO.2005.03.1484
-
Amar L, Bertherat J, Baudin E, et al. Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 2005; 23: 8812-8818. (Pubitemid 46211527)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.34
, 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..
-
17
-
-
0035992265
-
Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma
-
Dannenberg H, Dinjens WN, Abbou M, et al. Frequent germ-line succinate dehydrogenase subunit D gene mutations in patients with apparently sporadic parasympathetic paraganglioma. Clin Cancer Res 2002; 8: 2061-2066. (Pubitemid 34753574)
-
(2002)
Clinical Cancer Research
, vol.8
, Issue.7
, pp. 2061-2066
-
-
Dannenberg, H.1
Dinjens, W.N.M.2
Abbou, M.3
Van Urk, H.4
Pauw, B.K.H.5
Mouwen, D.6
Mooi, W.J.7
De Krijger, R.R.8
-
18
-
-
33845506053
-
Paragangliomas: Clinical overview
-
DOI 10.1196/annals.1353.002, Pheochromocytoma: First International Symposium
-
Young WF Jr,. Paragangliomas: clinical overview. Ann N Y Acad Sci 2006; 1073: 21-29. (Pubitemid 44911994)
-
(2006)
Annals of the New York Academy of Sciences
, vol.1073
, pp. 21-29
-
-
Young Jr., W.F.1
-
19
-
-
43349108023
-
Cervical paragangliomas: Is SDH genetic analysis systematically required?
-
Fakhry N, Niccoli-Sire P, Barlier-Seti A, Giorgi R, Giovanni A, Zanaret M,. Cervical paragangliomas: is SDH genetic analysis systematically required? Eur Arch Otorhinolaryngol 2008; 265: 557-563.
-
(2008)
Eur Arch Otorhinolaryngol
, vol.265
, pp. 557-563
-
-
Fakhry, N.1
Niccoli-Sire, P.2
Barlier-Seti, A.3
Giorgi, R.4
Giovanni, A.5
Zanaret, M.6
-
20
-
-
0344305801
-
On the association of succinate dehydrogenase mutations with hereditary paraganglioma
-
DOI 10.1016/j.tem.2003.08.004
-
Baysal BE,. On the association of succinate dehydrogenase mutations with hereditary paraganglioma. Trends Endocrinol Metab 2003; 14: 453-459. (Pubitemid 37517346)
-
(2003)
Trends in Endocrinology and Metabolism
, vol.14
, Issue.10
, pp. 453-459
-
-
Baysal, B.E.1
-
22
-
-
0034998621
-
Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene
-
DOI 10.1002/gcc.1144
-
Taschner PE, Jansen JC, Baysal BE, et al. Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene. Genes Chromosomes Cancer 2001; 31: 274-281. (Pubitemid 32521758)
-
(2001)
Genes Chromosomes and Cancer
, vol.31
, Issue.3
, pp. 274-281
-
-
Taschner, P.E.M.1
Jansen, J.C.2
Baysal, B.E.3
Bosch, A.4
Rosenberg, E.H.5
Brocker-Vriends, A.H.J.T.6
Van Der Mey, A.G.L.7
Van Ommen, G.-J.B.8
Cornelisse, C.J.9
Devilee, P.10
-
23
-
-
4444356015
-
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma
-
DOI 10.1136/jmg.2004.019224
-
Baysal BE, Willett-Brozick JE, Filho PA, Lawrence EC, Myers EN, Ferrell RE,. An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. J Med Genet 2004; 41: 703-709. (Pubitemid 39208612)
-
(2004)
Journal of Medical Genetics
, vol.41
, Issue.9
, pp. 703-709
-
-
Baysal, B.E.1
Willett-Brozick, J.E.2
Filho, P.A.A.3
Lawrence, E.C.4
Myers, E.N.5
Ferrell, R.E.6
-
24
-
-
66749179952
-
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2
-
Boedeker CC, Erlic Z, Richard S, et al. Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. J Clin Endocrinol Metab 2009; 94: 1938-1944.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 1938-1944
-
-
Boedeker, C.C.1
Erlic, Z.2
Richard, S.3
-
25
-
-
70449100913
-
Parasympathetic paragangliomas are part of the von Hippel-Lindau syndrome
-
Gaal J, van Nederveen FH, Erlic Z, et al. Parasympathetic paragangliomas are part of the Von Hippel-Lindau syndrome. J Clin Endocrinol Metab 2009; 94: 4367-4371.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 4367-4371
-
-
Gaal, J.1
Van Nederveen, F.H.2
Erlic, Z.3
-
26
-
-
77950342008
-
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma
-
Bayley JP, Kunst HP, Cascon A, et al. SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. Lancet Oncol 2010; 11: 366-372.
-
(2010)
Lancet Oncol
, vol.11
, pp. 366-372
-
-
Bayley, J.P.1
Kunst, H.P.2
Cascon, A.3
-
27
-
-
48749127110
-
In-octreotide is superior to 123I-metaiodobenzylguanidine for scintigraphic detection of head and neck paragangliomas
-
Koopmans KP, Jager PL, Kema IP, Kerstens MN, Albers F, Dullaart RP,. In-octreotide is superior to 123I-metaiodobenzylguanidine for scintigraphic detection of head and neck paragangliomas. J Nucl Med 2008; 49: 1232-1237.
-
(2008)
J Nucl Med
, vol.49
, pp. 1232-1237
-
-
Koopmans, K.P.1
Jager, P.L.2
Kema, I.P.3
Kerstens, M.N.4
Albers, F.5
Dullaart, R.P.6
|