-
2
-
-
33744771678
-
What we call them: The nomenclature of head and neck paragangliomas
-
Martin TP. What we call them: the nomenclature of head and neck paragangliomas. Clin Otolaryngol 2006;31:185-6.
-
(2006)
Clin Otolaryngol
, vol.31
, pp. 185-186
-
-
Martin, T.P.1
-
3
-
-
0019522666
-
Familial nonchromaffinic paragangliomas (glomus tumors): Clinical aspects
-
van Baars F, Van Den BP, Cremers C, Veldman J. Familial nonchromaffinic paragangliomas (glomus tumors) : clinical aspects. Laryngoscope 1981;91:988-96.
-
(1981)
Laryngoscope
, vol.91
, pp. 988-996
-
-
Van Baars, F.1
Van Den, B.P.2
Cremers, C.3
Veldman, J.4
-
4
-
-
0001969148
-
Familial and bilateral tumours of the carotic body
-
Chase W. Familial and bilateral tumours of the carotic body. J Pathol Bacteriol 1933;36:1-12.
-
(1933)
J Pathol Bacteriol
, vol.36
, pp. 1-12
-
-
Chase, W.1
-
5
-
-
0034790472
-
Proportion of heritable paraganglioma cases and associated clinical characteristics
-
Drovdlic CM, Myers EN, Peters JA, Baysal BE, Trackman DE, Slattery WH 3rd, et al. Proportion of heritable paraganglioma cases and associated clinical characteristics. Laryngoscope 2001;111:1822-7.
-
(2001)
Laryngoscope
, vol.111
, pp. 1822-1827
-
-
Drovdlic, C.M.1
Myers, E.N.2
Peters, J.A.3
Baysal, B.E.4
Trackman, D.E.5
Slattery III, W.H.6
-
6
-
-
0024404822
-
Genomic imprinting in hereditary glomus tumours: Evidence for new genetic theory
-
Van Der Mey AG, Maaswinkel-Mooy PD, Cornelisse CJ, Schmidt PH, van de Kamp JJ. Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory. Lancet 1989;2:1291-4.
-
(1989)
Lancet
, vol.2
, pp. 1291-1294
-
-
Van Der Mey, A.G.1
Maaswinkel-Mooy, P.D.2
Cornelisse, C.J.3
Schmidt, P.H.4
Van De Kamp, J.J.5
-
7
-
-
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, 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.
-
(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
-
8
-
-
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, et al. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science 2000;287:848-51.
-
(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
-
9
-
-
0033767445
-
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
-
Niemann S, Muller U. Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet 2000;26:268-70.
-
(2000)
Nat Genet
, vol.26
, pp. 268-270
-
-
Niemann, S.1
Muller, U.2
-
10
-
-
69549088424
-
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma
-
Hao HX, Khalimonchuk O, Schraders M, Dephoure N, Bayley JP, Kunst H, et al. SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma. Science 2009;325:1139-42.
-
(2009)
Science
, vol.325
, pp. 1139-1142
-
-
Hao, H.X.1
Khalimonchuk, O.2
Schraders, M.3
Dephoure, N.4
Bayley, J.P.5
Kunst, H.6
-
11
-
-
77958164441
-
SDHA is a tumor suppressor gene causing paraganglioma
-
Burnichon N, Brière JJ, Libé R, Vescovo L, Rivière J, Tissier F, et al. SDHA is a tumor suppressor gene causing paraganglioma. Hum Mol Genet 2010;19:3011-20.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 3011-3020
-
-
Burnichon, N.1
Brière, J.J.2
Libé, R.3
Vescovo, L.4
Rivière, J.5
Tissier, F.6
-
12
-
-
0027190801
-
Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q
-
Mariman EC, Van Beersum SE, Cremers CW, van Baars FM, Ropers HH. Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q. Hum Genet 1993;91:357-61.
-
(1993)
Hum Genet
, vol.91
, pp. 357-361
-
-
Mariman, E.C.1
Van Beersum, S.E.2
Cremers, C.W.3
Van Baars, F.M.4
Ropers, H.H.5
-
13
-
-
2942561954
-
Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families
-
Hensen EF, Jordanova ES, van Minderhout IJ, Hogendoorn PC, Taschner PE, van der Mey AG, et al. Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families. Oncogene 2004;23:4076-83.
-
(2004)
Oncogene
, vol.23
, pp. 4076-4083
-
-
Hensen, E.F.1
Jordanova, E.S.2
Van Minderhout, I.J.3
Hogendoorn, P.C.4
Taschner, P.E.5
Van Der Mey, A.G.6
-
14
-
-
50449095151
-
The H19 locus acts in vivo as a tumor suppressor
-
Yoshimizu T, Miroglio A, Ripoche MA, Gabory A, Vernucci M, Riccio A, et al. The H19 locus acts in vivo as a tumor suppressor. Proc Natl Acad Sci U S A 2008;105:12417-22.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 12417-12422
-
-
Yoshimizu, T.1
Miroglio, A.2
Ripoche, M.A.3
Gabory, A.4
Vernucci, M.5
Riccio, A.6
-
15
-
-
0036468725
-
National cancer data base report on malignant paragangliomas of the head and neck
-
DOI 10.1002/cncr.10252
-
Lee JH, Barich F, Karnell LH, Robinson RA, Zhen WK, Gantz BJ, et al. National Cancer Data Base report on malignant paragangliomas of the head and neck. Cancer 2002;94:730-7. (Pubitemid 34132302)
-
(2002)
Cancer
, vol.94
, Issue.3
, pp. 730-737
-
-
Lee, J.H.1
Barich, F.2
Karnell, L.H.3
Robinson, R.A.4
Zhen, W.K.5
Gantz, B.J.6
Hoffman, H.T.7
-
16
-
-
34250787602
-
Malignant head and neck paragangliomas in SDHB mutation carriers
-
Boedeker CC, Neumann HP, Maier W, Bausch B, Schipper J, Ridder GJ. Malignant head and neck paragangliomas in SDHB mutation carriers. Otolaryngol Head Neck Surg 2007;137:126-9.
-
(2007)
Otolaryngol Head Neck Surg
, vol.137
, pp. 126-129
-
-
Boedeker, C.C.1
Neumann, H.P.2
Maier, W.3
Bausch, B.4
Schipper, J.5
Ridder, G.J.6
-
17
-
-
0031397846
-
Glomus tumours and genomic imprinting: Influence of inheritance along the paternal or maternal line
-
Struycken PM, Cremers CW, Mariman EC, Joosten FB, Bleker RJ. Glomus tumours and genomic imprinting: influence of inheritance along the paternal or maternal line. Clin Otolaryngol Allied Sci 1997;22:71-6.
-
(1997)
Clin Otolaryngol Allied Sci
, vol.22
, pp. 71-76
-
-
Struycken, P.M.1
Cremers, C.W.2
Mariman, E.C.3
Joosten, F.B.4
Bleker, R.J.5
-
18
-
-
0028809123
-
Fine mapping of a putatively imprinted gene for familial nonchromaffin paragangliomas to chromosome 11q13.1: Evidence for genetic heterogeneity
-
Mariman EC, Van Beersum SE, Cremers CW, Struycken PM, Ropers HH. Fine mapping of a putatively imprinted gene for familial nonchromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneity. Hum Genet 1995;95:56-62.
-
(1995)
Hum Genet
, vol.95
, pp. 56-62
-
-
Mariman, E.C.1
Van Beersum, S.E.2
Cremers, C.W.3
Struycken, P.M.4
Ropers, H.H.5
-
19
-
-
0019993995
-
Genetic aspects of nonchromaffin paraganglioma
-
van Baars F, Cremers C, Van Den BP, Geerts S, Veldman J. Genetic aspects of nonchromaffin paraganglioma. Hum Genet 1982; 60:305-9.
-
(1982)
Hum Genet
, vol.60
, pp. 305-309
-
-
Van Baars, F.1
Cremers, C.2
Van Den, B.P.3
Geerts, S.4
Veldman, J.5
-
20
-
-
33845506053
-
Paragangliomas: Clinical overview
-
Young WF Jr. Paragangliomas: clinical overview. Ann N Y Acad Sci 2006;1073:21-9.
-
(2006)
Ann N Y Acad Sci
, vol.1073
, pp. 21-29
-
-
Young Jr., W.F.1
-
21
-
-
0034659890
-
Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal
-
Jansen JC, Van Den BR, Kuiper A, Van Der Mey AG, Zwinderman AH, Cornelisse CJ. Estimation of growth rate in patients with head and neck paragangliomas influences the treatment proposal. Cancer 2000;88:2811-6.
-
(2000)
Cancer
, vol.88
, pp. 2811-2816
-
-
Jansen, J.C.1
Van Den, B.R.2
Kuiper, A.3
Van Der Mey, A.G.4
Zwinderman, A.H.5
Cornelisse, C.J.6
-
22
-
-
79251527706
-
Inherited diseases: Miscellaneous paraganglioma
-
Nijmegen, the Netherlands: Remedica
-
Kunst D, Kremer H, Cremers C. Inherited diseases: miscellaneous paraganglioma. In Genetics For ENT Specialists. Nijmegen, the Netherlands: Remedica;2005:p.165-71.
-
(2005)
Genetics for ENT Specialists
, pp. 165-171
-
-
Kunst, D.1
Kremer, H.2
Cremers, C.3
-
23
-
-
0031690675
-
Vagal paraganglioma: A review of 46 patients treated during a 20-year period
-
Netterville JL, Jackson CG, Miller FR, Wanamaker JR, Glasscock ME. Vagal paraganglioma: a review of 46 patients treated during a 20-year period. Arch Otolaryngol Head Neck Surg 1998;124:1133-40.
-
(1998)
Arch Otolaryngol Head Neck Surg
, vol.124
, pp. 1133-1140
-
-
Netterville, J.L.1
Jackson, C.G.2
Miller, F.R.3
Wanamaker, J.R.4
Glasscock, M.E.5
-
24
-
-
0037133568
-
Long-term effects of carotid sinus denervation on arterial blood pressure in humans
-
Smit AA, Timmers HJ, Wieling W, Wagenaar M, Marres HA, Lenders JW, et al. Long-term effects of carotid sinus denervation on arterial blood pressure in humans. Circulation 2002;105:1329-35.
-
(2002)
Circulation
, vol.105
, pp. 1329-1335
-
-
Smit, A.A.1
Timmers, H.J.2
Wieling, W.3
Wagenaar, M.4
Marres, H.A.5
Lenders, J.W.6
-
25
-
-
0023832438
-
Trends in neurovascular complications of surgical management for carotid body and cervical paragangliomas: A fifty-year experience with 153 tumors
-
Hallett JW Jr., Nora JD, Hollier LH, Cherry KJ Jr., Pairolero PC. Trends in neurovascular complications of surgical management for carotid body and cervical paragangliomas: a fifty-year experience with 153 tumors . J Vasc Surg 1988;7:284-91.
-
(1988)
J Vasc Surg
, vol.7
, pp. 284-291
-
-
Hallett Jr., J.W.1
Nora, J.D.2
Hollier, L.H.3
Cherry Jr., K.J.4
Pairolero, P.C.5
-
26
-
-
56049122457
-
Clinical and molecular progress in hereditary paraganglioma
-
Baysal BE. Clinical and molecular progress in hereditary paraganglioma. J Med Genet 2008 ;45:689-94.
-
(2008)
J Med Genet
, vol.45
, pp. 689-694
-
-
Baysal, B.E.1
-
27
-
-
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, et al. Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations. JAMA 2004;292:943-51.
-
(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
-
28
-
-
34147106160
-
Malignant paragangliomas associated with mutations in the succinate dehydrogenase D gene
-
Havekes B, Corssmit EP, Jansen JC, Van Der Mey AG, Vriends AH, Romijn JA. Malignant paragangliomas associated with mutations in the succinate dehydrogenase D gene. J Clin Endocrinol Metab 2007;92:1245-8.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 1245-1248
-
-
Havekes, B.1
Corssmit, E.P.2
Jansen, J.C.3
Van Der Mey, A.G.4
Vriends, A.H.5
Romijn, J.A.6
-
29
-
-
33644822473
-
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes
-
Benn DE, Gimenez-Roqueplo AP, Reilly JR, Bertherat J, Burgess J, Byth K, et al. Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes. J Clin Endocrinol Metab 2006;91:827-36.
-
(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
-
30
-
-
0037594892
-
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC
-
Niemann S, Muller U, Engelhardt D, Lohse P. Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. Hum Genet 2003;113:92-4. (Pubitemid 36869043)
-
(2003)
Human Genetics
, vol.113
, Issue.1
, pp. 92-94
-
-
Niemann, S.1
Muller, U.2
Engelhardt, D.3
Lohse, P.4
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