-
1
-
-
84902310939
-
Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline
-
Lenders JW, Duh QY, Eisenhofer G, Gimenez-Roqueplo AP, Grebe SK, Murad MH, Naruse M, Pacak K, Young WF Jr. Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 2014;99:1915-42.
-
(2014)
J Clin Endocrinol Metab
, vol.99
, pp. 1915-1942
-
-
Lenders, J.W.1
Duh, Q.Y.2
Eisenhofer, G.3
Gimenez-Roqueplo, A.P.4
Grebe, S.K.5
Murad, M.H.6
Naruse, M.7
Pacak, K.8
Young, W.F.9
-
2
-
-
84894556457
-
Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity
-
Dahia PL. Pheochromocytoma and paraganglioma pathogenesis: learning from genetic heterogeneity. Nat Rev Cancer 2014;14:108-19.
-
(2014)
Nat Rev Cancer
, vol.14
, pp. 108-119
-
-
Dahia, P.L.1
-
3
-
-
84923081697
-
Paraganglioma and phaeochromocytoma: from genetics to personalized medicine
-
Favier J, Amar L, Gimenez-Roqueplo AP. Paraganglioma and phaeochromocytoma: from genetics to personalized medicine. Nat Rev Endocrinol 2015;11:101-11.
-
(2015)
Nat Rev Endocrinol
, vol.11
, pp. 101-111
-
-
Favier, J.1
Amar, L.2
Gimenez-Roqueplo, A.P.3
-
4
-
-
0025326726
-
A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
-
Cawthon RM, Weiss R, Xu GF, Viskochil D, Culver M, Stevens J, Robertson M, Dunn D, Gesteland R, O'Connell P. A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. Cell 1990;62:193-201.
-
(1990)
Cell
, vol.62
, pp. 193-201
-
-
Cawthon, R.M.1
Weiss, R.2
Xu, G.F.3
Viskochil, D.4
Culver, M.5
Stevens, J.6
Robertson, M.7
Dunn, D.8
Gesteland, R.9
O'Connell, P.10
-
5
-
-
84896052975
-
Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment
-
Martucci VL, Pacak K. Pheochromocytoma and paraganglioma: diagnosis, genetics, management, and treatment. Curr Probl Cancer 2014;38:7-41.
-
(2014)
Curr Probl Cancer
, vol.38
, pp. 7-41
-
-
Martucci, V.L.1
Pacak, K.2
-
6
-
-
34447520170
-
Somatic SDHB mutation in an extraadrenal pheochromocytoma
-
van Nederveen FH, Korpershoek E, Lenders JW, de Krijger RR, Dinjens WN. Somatic SDHB mutation in an extraadrenal pheochromocytoma. N Engl J Med 2007;357:306-8.
-
(2007)
N Engl J Med
, vol.357
, pp. 306-308
-
-
van Nederveen, F.H.1
Korpershoek, E.2
Lenders, J.W.3
de Krijger, R.R.4
Dinjens, W.N.5
-
7
-
-
84855940667
-
Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas
-
Welander J, Soderkvist P, Gimm O. Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas. Endocr Relat Cancer 2011;18:R253-76.
-
(2011)
Endocr Relat Cancer
, vol.18
, pp. R253-R276
-
-
Welander, J.1
Soderkvist, P.2
Gimm, O.3
-
8
-
-
84926681391
-
Germ-line PHD1 and PHD2 mutations detected in patients with pheochromocytoma/ paraganglioma-polycythemia
-
Yang C, Zhuang Z, Fliedner SM, Shankavaram U, Sun MG, Bullova P, Zhu R, Elkahloun AG, Kourlas PJ, Merino M, Kebebew E, Pacak K. Germ-line PHD1 and PHD2 mutations detected in patients with pheochromocytoma/ paraganglioma-polycythemia. J Mol Med (Berl) 2015;93:93-104.
-
(2015)
J Mol Med (Berl)
, vol.93
, pp. 93-104
-
-
Yang, C.1
Zhuang, Z.2
Fliedner, S.M.3
Shankavaram, U.4
Sun, M.G.5
Bullova, P.6
Zhu, R.7
Elkahloun, A.G.8
Kourlas, P.J.9
Merino, M.10
Kebebew, E.11
Pacak, K.12
-
9
-
-
84928430437
-
Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene
-
djv053
-
Cascon A, Comino-Mendez I, Curras-Freixes M, de Cubas AA, Contreras L, Richter S, Peitzsch M, Mancikova V, Inglada-Perez L, Perez-Barrios A, Calatayud M, Azriel S, Villar-Vicente R, Aller J, Setien F, Moran S, Garcia JF, Rio-Machin A, Leton R, Gomez-Grana A, Apellaniz-Ruiz M, Roncador G, Esteller M, Rodriguez-Antona C, Satrustegui J, Eisenhofer G, Urioste M, Robledo M. Whole-exome sequencing identifies MDH2 as a new familial paraganglioma gene. J Natl Cancer Inst 2015;107. pii: djv053.
-
(2015)
J Natl Cancer Inst
, vol.107
-
-
Cascon, A.1
Comino-Mendez, I.2
Curras-Freixes, M.3
de Cubas, A.A.4
Contreras, L.5
Richter, S.6
Peitzsch, M.7
Mancikova, V.8
Inglada-Perez, L.9
Perez-Barrios, A.10
Calatayud, M.11
Azriel, S.12
Villar-Vicente, R.13
Aller, J.14
Setien, F.15
Moran, S.16
Garcia, J.F.17
Rio-Machin, A.18
Leton, R.19
Gomez-Grana, A.20
Apellaniz-Ruiz, M.21
Roncador, G.22
Esteller, M.23
Rodriguez-Antona, C.24
Satrustegui, J.25
Eisenhofer, G.26
Urioste, M.27
Robledo, M.28
more..
-
10
-
-
84928566914
-
Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas
-
Fishbein L, Khare S, Wubbenhorst B, DeSloover D, D'Andrea K, Merrill S, Cho NW, Greenberg RA, Else T, Montone K, LiVolsi V, Fraker D, Daber R, Cohen DL, Nathanson KL. Whole-exome sequencing identifies somatic ATRX mutations in pheochromocytomas and paragangliomas. Nat Commun 2015;6:6140.
-
(2015)
Nat Commun
, vol.6
, pp. 6140
-
-
Fishbein, L.1
Khare, S.2
Wubbenhorst, B.3
DeSloover, D.4
D'Andrea, K.5
Merrill, S.6
Cho, N.W.7
Greenberg, R.A.8
Else, T.9
Montone, K.10
LiVolsi, V.11
Fraker, D.12
Daber, R.13
Cohen, D.L.14
Nathanson, K.L.15
-
11
-
-
84926609624
-
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis
-
Luchetti A, Walsh D, Rodger F, Clark G, Martin T, Irving R, Sanna M, Yao M, Robledo M, Neumann HP, Woodward ER, Latif F, Abbs S, Martin H, Maher ER. Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis. Int J Endocrinol 2015;2015:138573.
-
(2015)
Int J Endocrinol
, vol.2015
-
-
Luchetti, A.1
Walsh, D.2
Rodger, F.3
Clark, G.4
Martin, T.5
Irving, R.6
Sanna, M.7
Yao, M.8
Robledo, M.9
Neumann, H.P.10
Woodward, E.R.11
Latif, F.12
Abbs, S.13
Martin, H.14
Maher, E.R.15
-
12
-
-
33748755275
-
Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma
-
Bausch B, Koschker AC, Fassnacht M, Stoevesandt J, Hoffmann MM, Eng C, Allolio B, Neumann HP. Comprehensive mutation scanning of NF1 in apparently sporadic cases of pheochromocytoma. J Clin Endocrinol Metab 2006;91:3478-81.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 3478-3481
-
-
Bausch, B.1
Koschker, A.C.2
Fassnacht, M.3
Stoevesandt, J.4
Hoffmann, M.M.5
Eng, C.6
Allolio, B.7
Neumann, H.P.8
-
13
-
-
70350217774
-
Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients
-
Erlic Z, Rybicki L, Peczkowska M, Golcher H, Kann PH, Brauckhoff M, Mussig K, Muresan M, Schaffler A, Reisch N, Schott M, Fassnacht M, Opocher G, Klose S, Fottner C, Forrer F, Plockinger U, Petersenn S, Zabolotny D, Kollukch O, Yaremchuk S, Januszewicz A, Walz MK, Eng C, Neumann HP. Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. Clin Cancer Res 2009;15:6378-85.
-
(2009)
Clin Cancer Res
, vol.15
, pp. 6378-6385
-
-
Erlic, Z.1
Rybicki, L.2
Peczkowska, M.3
Golcher, H.4
Kann, P.H.5
Brauckhoff, M.6
Mussig, K.7
Muresan, M.8
Schaffler, A.9
Reisch, N.10
Schott, M.11
Fassnacht, M.12
Opocher, G.13
Klose, S.14
Fottner, C.15
Forrer, F.16
Plockinger, U.17
Petersenn, S.18
Zabolotny, D.19
Kollukch, O.20
Yaremchuk, S.21
Januszewicz, A.22
Walz, M.K.23
Eng, C.24
Neumann, H.P.25
more..
-
14
-
-
66149098136
-
Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas
-
Mannelli M, Castellano M, Schiavi F, Filetti S, Giacche M, Mori L, Pignataro V, Bernini G, Giache V, Bacca A, Biondi B, Corona G, Di Trapani G, Grossrubatscher E, Reimondo G, Arnaldi G, Giacchetti G, Veglio F, Loli P, Colao A, Ambrosio MR, Terzolo M, Letizia C, Ercolino T, Opocher G. Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas. J Clin Endocrinol Metab 2009;94:1541-7.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 1541-1547
-
-
Mannelli, M.1
Castellano, M.2
Schiavi, F.3
Filetti, S.4
Giacche, M.5
Mori, L.6
Pignataro, V.7
Bernini, G.8
Giache, V.9
Bacca, A.10
Biondi, B.11
Corona, G.12
Di Trapani, G.13
Grossrubatscher, E.14
Reimondo, G.15
Arnaldi, G.16
Giacchetti, G.17
Veglio, F.18
Loli, P.19
Colao, A.20
Ambrosio, M.R.21
Terzolo, M.22
Letizia, C.23
Ercolino, T.24
Opocher, G.25
more..
-
15
-
-
70350211961
-
Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma
-
Cascon A, Lopez-Jimenez E, Landa I, Leskela S, Leandro-Garcia LJ, Maliszewska A, Leton R, de la Vega L, Garcia-Barcina MJ, Sanabria C, Alvarez-Escola C, Rodriguez-Antona C, Robledo M. Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma. Horm Metab Res 2009;41:672-5.
-
(2009)
Horm Metab Res
, vol.41
, pp. 672-675
-
-
Cascon, A.1
Lopez-Jimenez, E.2
Landa, I.3
Leskela, S.4
Leandro-Garcia, L.J.5
Maliszewska, A.6
Leton, R.7
de la Vega, L.8
Garcia-Barcina, M.J.9
Sanabria, C.10
Alvarez-Escola, C.11
Rodriguez-Antona, C.12
Robledo, M.13
-
16
-
-
84901754693
-
Paragangliomas/pheochromocytomas: clinically oriented genetic testing
-
Martins R, Bugalho MJ. Paragangliomas/pheochromocytomas: clinically oriented genetic testing. Int J Endocrinol 2014;2014:794187.
-
(2014)
Int J Endocrinol
, vol.2014
, pp. 794187
-
-
Martins, R.1
Bugalho, M.J.2
-
17
-
-
84923069909
-
Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review
-
Brito JP, Asi N, Bancos I, Gionfriddo MR, Zeballos-Palacios CL, Leppin AL, Undavalli C, Wang Z, Domecq JP, Prustsky G, Elraiyah TA, Prokop LJ, Montori VM, Murad MH. Testing for germline mutations in sporadic pheochromocytoma/paraganglioma: a systematic review. Clin Endocrinol (Oxf) 2015;82:338-45.
-
(2015)
Clin Endocrinol (Oxf)
, vol.82
, pp. 338-345
-
-
Brito, J.P.1
Asi, N.2
Bancos, I.3
Gionfriddo, M.R.4
Zeballos-Palacios, C.L.5
Leppin, A.L.6
Undavalli, C.7
Wang, Z.8
Domecq, J.P.9
Prustsky, G.10
Elraiyah, T.A.11
Prokop, L.J.12
Montori, V.M.13
Murad, M.H.14
-
18
-
-
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. Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 2005;23:8812-18.
-
(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..
-
19
-
-
0037046659
-
Germ-line mutations in nonsyndromic pheochromocytoma
-
Neumann HP, Bausch B, McWhinney SR, Bender BU, Gimm O, Franke G, Schipper J, Klisch J, Altehoefer C, Zerres K, Januszewicz A, Eng C, Smith WM, Munk R, Manz T, Glaesker S, Apel TW, Treier M, Reineke M, Walz MK, Hoang-Vu C, Brauckhoff M, Klein-Franke A, Klose P, Schmidt H, Maier-Woelfle M, Peczkowska M, Szmigielski C. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 2002;346:1459-66.
-
(2002)
N Engl J Med
, vol.346
, pp. 1459-1466
-
-
Neumann, H.P.1
Bausch, B.2
McWhinney, S.R.3
Bender, B.U.4
Gimm, O.5
Franke, G.6
Schipper, J.7
Klisch, J.8
Altehoefer, C.9
Zerres, K.10
Januszewicz, A.11
Eng, C.12
Smith, W.M.13
Munk, R.14
Manz, T.15
Glaesker, S.16
Apel, T.W.17
Treier, M.18
Reineke, M.19
Walz, M.K.20
Hoang-Vu, C.21
Brauckhoff, M.22
Klein-Franke, A.23
Klose, P.24
Schmidt, H.25
Maier-Woelfle, M.26
Peczkowska, M.27
Szmigielski, C.28
more..
-
20
-
-
66149142195
-
Genetics of pheochromocytoma and paraganglioma in Spanish patients
-
Cascon A, Pita G, Burnichon N, Landa I, Lopez-Jimenez E, Montero-Conde C, Leskela S, Leandro-Garcia LJ, Leton R, Rodriguez-Antona C, Diaz JA, Lopez-Vidriero E, Gonzalez-Neira A, Velasco A, Matias-Guiu X, Gimenez-Roqueplo AP, Robledo M. Genetics of pheochromocytoma and paraganglioma in Spanish patients. J Clin Endocrinol Metab 2009;94:1701-5.
-
(2009)
J Clin Endocrinol Metab
, vol.94
, pp. 1701-1705
-
-
Cascon, A.1
Pita, G.2
Burnichon, N.3
Landa, I.4
Lopez-Jimenez, E.5
Montero-Conde, C.6
Leskela, S.7
Leandro-Garcia, L.J.8
Leton, R.9
Rodriguez-Antona, C.10
Diaz, J.A.11
Lopez-Vidriero, E.12
Gonzalez-Neira, A.13
Velasco, A.14
Matias-Guiu, X.15
Gimenez-Roqueplo, A.P.16
Robledo, M.17
-
21
-
-
80053139912
-
Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma
-
Burnichon N, Vescovo L, Amar L, Libe R, de Reynies A, Venisse A, Jouanno E, Laurendeau I, Parfait B, Bertherat J, Plouin PF, Jeunemaitre X, Favier J, Gimenez-Roqueplo AP. Integrative genomic analysis reveals somatic mutations in pheochromocytoma and paraganglioma. Hum Mol Genet 2011;20:3974-85.
-
(2011)
Hum Mol Genet
, vol.20
, pp. 3974-3985
-
-
Burnichon, N.1
Vescovo, L.2
Amar, L.3
Libe, R.4
de Reynies, A.5
Venisse, A.6
Jouanno, E.7
Laurendeau, I.8
Parfait, B.9
Bertherat, J.10
Plouin, P.F.11
Jeunemaitre, X.12
Favier, J.13
Gimenez-Roqueplo, A.P.14
-
22
-
-
84870004468
-
Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma
-
Burnichon N, Buffet A, Parfait B, Letouze E, Laurendeau I, Loriot C, Pasmant E, Abermil N, Valeyrie-Allanore L, Bertherat J, Amar L, Vidaud D, Favier J, Gimenez-Roqueplo AP. Somatic NF1 inactivation is a frequent event in sporadic pheochromocytoma. Hum Mol Genet 2012;21:5397-405.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 5397-5405
-
-
Burnichon, N.1
Buffet, A.2
Parfait, B.3
Letouze, E.4
Laurendeau, I.5
Loriot, C.6
Pasmant, E.7
Abermil, N.8
Valeyrie-Allanore, L.9
Bertherat, J.10
Amar, L.11
Vidaud, D.12
Favier, J.13
Gimenez-Roqueplo, A.P.14
-
23
-
-
84870801743
-
Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas
-
Welander J, Larsson C, Backdahl M, Hareni N, Sivler T, Brauckhoff M, Soderkvist P, Gimm O. Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas. Hum Mol Genet 2012;21:5406-16.
-
(2012)
Hum Mol Genet
, vol.21
, pp. 5406-5416
-
-
Welander, J.1
Larsson, C.2
Backdahl, M.3
Hareni, N.4
Sivler, T.5
Brauckhoff, M.6
Soderkvist, P.7
Gimm, O.8
-
24
-
-
84879920967
-
Somatic mutations in H-RAS in sporadic pheochromocytoma and paraganglioma identified by exome sequencing
-
Crona J, Delgado Verdugo A, Maharjan R, Stalberg P, Granberg D, Hellman P, Bjorklund P. Somatic mutations in H-RAS in sporadic pheochromocytoma and paraganglioma identified by exome sequencing. J Clin Endocrinol Metab 2013;98: E1266-71.
-
(2013)
J Clin Endocrinol Metab
, vol.98
, pp. E1266-E1271
-
-
Crona, J.1
Delgado Verdugo, A.2
Maharjan, R.3
Stalberg, P.4
Granberg, D.5
Hellman, P.6
Bjorklund, P.7
-
25
-
-
84861140704
-
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
-
Burnichon N, Cascon A, Schiavi F, Morales NP, Comino-Mendez I, Abermil N, Inglada-Perez L, de Cubas AA, Amar L, Barontini M, de Quiros SB, Bertherat J, Bignon YJ, Blok MJ, Bobisse S, Borrego S, Castellano M, Chanson P, Chiara MD, Corssmit EP, Giacche M, de Krijger RR, Ercolino T, Girerd X, Gomez-Garcia EB, Gomez-Grana A, Guilhem I, Hes FJ, Honrado E, Korpershoek E, Lenders JW, Leton R, Mensenkamp AR, Merlo A, Mori L, Murat A, Pierre P, Plouin PF, Prodanov T, Quesada-Charneco M, Qin N, Rapizzi E, Raymond V, Reisch N, Roncador G, Ruiz-Ferrer M, Schillo F, Stegmann AP, Suarez C, Taschin E, Timmers HJ, Tops CM, Urioste M, Beuschlein F, Pacak K, Mannelli M, Dahia PL, Opocher G, Eisenhofer G, Gimenez-Roqueplo AP, Robledo M. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma. Clin Cancer Res 2012;18:2828-37.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 2828-2837
-
-
Burnichon, N.1
Cascon, A.2
Schiavi, F.3
Morales, N.P.4
Comino-Mendez, I.5
Abermil, N.6
Inglada-Perez, L.7
de Cubas, A.A.8
Amar, L.9
Barontini, M.10
de Quiros, S.B.11
Bertherat, J.12
Bignon, Y.J.13
Blok, M.J.14
Bobisse, S.15
Borrego, S.16
Castellano, M.17
Chanson, P.18
Chiara, M.D.19
Corssmit, E.P.20
Giacche, M.21
de Krijger, R.R.22
Ercolino, T.23
Girerd, X.24
Gomez-Garcia, E.B.25
Gomez-Grana, A.26
Guilhem, I.27
Hes, F.J.28
Honrado, E.29
Korpershoek, E.30
Lenders, J.W.31
Leton, R.32
Mensenkamp, A.R.33
Merlo, A.34
Mori, L.35
Murat, A.36
Pierre, P.37
Plouin, P.F.38
Prodanov, T.39
Quesada-Charneco, M.40
Qin, N.41
Rapizzi, E.42
Raymond, V.43
Reisch, N.44
Roncador, G.45
Ruiz-Ferrer, M.46
Schillo, F.47
Stegmann, A.P.48
Suarez, C.49
Taschin, E.50
Timmers, H.J.51
Tops, C.M.52
Urioste, M.53
Beuschlein, F.54
Pacak, K.55
Mannelli, M.56
Dahia, P.L.57
Opocher, G.58
Eisenhofer, G.59
Gimenez-Roqueplo, A.P.60
Robledo, M.61
more..
-
26
-
-
84904035130
-
H-RAS mutations are restricted to sporadic pheochromocytomas lacking specific clinical or pathological features: data from a multi-institutional series
-
Oudijk L, de Krijger RR, Rapa I, Beuschlein F, de Cubas AA, Dei Tos AP, Dinjens WN, Korpershoek E, Mancikova V, Mannelli M, Papotti M, Vatrano S, Robledo M, Volante M. H-RAS mutations are restricted to sporadic pheochromocytomas lacking specific clinical or pathological features: data from a multi-institutional series. J Clin Endocrinol Metab 2014;99:E1376-80.
-
(2014)
J Clin Endocrinol Metab
, vol.99
, pp. E1376-E1380
-
-
Oudijk, L.1
de Krijger, R.R.2
Rapa, I.3
Beuschlein, F.4
de Cubas, A.A.5
Dei Tos, A.P.6
Dinjens, W.N.7
Korpershoek, E.8
Mancikova, V.9
Mannelli, M.10
Papotti, M.11
Vatrano, S.12
Robledo, M.13
Volante, M.14
-
27
-
-
84904061756
-
Universal genetic screening uncovers a novel presentation of an SDHAF2 mutation
-
Casey R, Garrahy A, Tuthill A, O'Halloran D, Joyce C, Casey MB, O'Shea P, Bell M. Universal genetic screening uncovers a novel presentation of an SDHAF2 mutation. J Clin Endocrinol Metab 2014;99:E1392-6.
-
(2014)
J Clin Endocrinol Metab
, vol.99
, pp. E1392-E1396
-
-
Casey, R.1
Garrahy, A.2
Tuthill, A.3
O'Halloran, D.4
Joyce, C.5
Casey, M.B.6
O'Shea, P.7
Bell, M.8
-
28
-
-
84879922796
-
A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma
-
Rattenberry E, Vialard L, Yeung A, Bair H, McKay K, Jafri M, Canham N, Cole TR, Denes J, Hodgson SV, Irving R, Izatt L, Korbonits M, Kumar AV, Lalloo F, Morrison PJ, Woodward ER, Macdonald F, Wallis Y, Maher ER. A comprehensive next generation sequencing-based genetic testing strategy to improve diagnosis of inherited pheochromocytoma and paraganglioma. J Clin Endocrinol Metab 2013;98: E1248-56.
-
(2013)
J Clin Endocrinol Metab
, vol.98
, pp. E1248-E1256
-
-
Rattenberry, E.1
Vialard, L.2
Yeung, A.3
Bair, H.4
McKay, K.5
Jafri, M.6
Canham, N.7
Cole, T.R.8
Denes, J.9
Hodgson, S.V.10
Irving, R.11
Izatt, L.12
Korbonits, M.13
Kumar, A.V.14
Lalloo, F.15
Morrison, P.J.16
Woodward, E.R.17
Macdonald, F.18
Wallis, Y.19
Maher, E.R.20
more..
-
29
-
-
84903613822
-
Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma
-
Welander J, Andreasson A, Juhlin CC, Wiseman RW, Backdahl M, Hoog A, Larsson C, Gimm O, Soderkvist P. Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma. J Clin Endocrinol Metab 2014;99:E1352-60.
-
(2014)
J Clin Endocrinol Metab
, vol.99
, pp. E1352-E1360
-
-
Welander, J.1
Andreasson, A.2
Juhlin, C.C.3
Wiseman, R.W.4
Backdahl, M.5
Hoog, A.6
Larsson, C.7
Gimm, O.8
Soderkvist, P.9
-
30
-
-
84899523491
-
Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours
-
Crona J, Nordling M, Maharjan R, Granberg D, Stalberg P, Hellman P, Bjorklund P. Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours. PLoS One 2014;9:e86756.
-
(2014)
PLoS One
, vol.9
, pp. e86756
-
-
Crona, J.1
Nordling, M.2
Maharjan, R.3
Granberg, D.4
Stalberg, P.5
Hellman, P.6
Bjorklund, P.7
-
31
-
-
80052540617
-
SDHA immunohistochemistry detects germline SDHA gene mutations in apparently sporadic paragangliomas and pheochromocytomas
-
Korpershoek E, Favier J, Gaal J, Burnichon N, van Gessel B, Oudijk L, Badoual C, Gadessaud N, Venisse A, Bayley JP, van Dooren MF, de Herder WW, Tissier F, Plouin PF, van Nederveen FH, Dinjens WN, Gimenez-Roqueplo AP, de Krijger RR. SDHA immunohistochemistry detects germline SDHA gene mutations in apparently sporadic paragangliomas and pheochromocytomas. J Clin Endocrinol Metab 2011;96:E1472-6.
-
(2011)
J Clin Endocrinol Metab
, vol.96
, pp. E1472-E1476
-
-
Korpershoek, E.1
Favier, J.2
Gaal, J.3
Burnichon, N.4
van Gessel, B.5
Oudijk, L.6
Badoual, C.7
Gadessaud, N.8
Venisse, A.9
Bayley, J.P.10
van Dooren, M.F.11
de Herder, W.W.12
Tissier, F.13
Plouin, P.F.14
van Nederveen, F.H.15
Dinjens, W.N.16
Gimenez-Roqueplo, A.P.17
de Krijger, R.R.18
-
32
-
-
67651198212
-
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis
-
van Nederveen FH, Gaal J, Favier J, Korpershoek E, Oldenburg RA, de Bruyn EM, Sleddens HF, Derkx P, Riviere J, Dannenberg H, Petri BJ, Komminoth P, Pacak K, Hop WC, Pollard PJ, Mannelli M, Bayley JP, Perren A, Niemann S, Verhofstad AA, de Bruine AP, Maher ER, Tissier F, Meatchi T, Badoual C, Bertherat J, Amar L, Alataki D, Van Marck E, Ferrau F, Francois J, de Herder WW, Peeters MP, van Linge A, Lenders JW, Gimenez-Roqueplo AP, de Krijger RR, Dinjens WN. An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis. Lancet Oncol 2009;10:764-71.
-
(2009)
Lancet Oncol
, vol.10
, pp. 764-771
-
-
van Nederveen, F.H.1
Gaal, J.2
Favier, J.3
Korpershoek, E.4
Oldenburg, R.A.5
de Bruyn, E.M.6
Sleddens, H.F.7
Derkx, P.8
Riviere, J.9
Dannenberg, H.10
Petri, B.J.11
Komminoth, P.12
Pacak, K.13
Hop, W.C.14
Pollard, P.J.15
Mannelli, M.16
Bayley, J.P.17
Perren, A.18
Niemann, S.19
Verhofstad, A.A.20
de Bruine, A.P.21
Maher, E.R.22
Tissier, F.23
Meatchi, T.24
Badoual, C.25
Bertherat, J.26
Amar, L.27
Alataki, D.28
Van Marck, E.29
Ferrau, F.30
Francois, J.31
de Herder, W.W.32
Peeters, M.P.33
van Linge, A.34
Lenders, J.W.35
Gimenez-Roqueplo, A.P.36
de Krijger, R.R.37
Dinjens, W.N.38
more..
-
34
-
-
78650200503
-
Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas
-
Yao L, Schiavi F, Cascon A, Qin Y, Inglada-Perez L, King EE, Toledo RA, Ercolino T, Rapizzi E, Ricketts CJ, Mori L, Giacche M, Mendola A, Taschin E, Boaretto F, Loli P, Iacobone M, Rossi GP, Biondi B, Lima-Junior JV, Kater CE, Bex M, Vikkula M, Grossman AB, Gruber SB, Barontini M, Persu A, Castellano M, Toledo SP, Maher ER, Mannelli M, Opocher G, Robledo M, Dahia PL. Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas. JAMA 2010;304:2611-19.
-
(2010)
JAMA
, vol.304
, pp. 2611-2619
-
-
Yao, L.1
Schiavi, F.2
Cascon, A.3
Qin, Y.4
Inglada-Perez, L.5
King, E.E.6
Toledo, R.A.7
Ercolino, T.8
Rapizzi, E.9
Ricketts, C.J.10
Mori, L.11
Giacche, M.12
Mendola, A.13
Taschin, E.14
Boaretto, F.15
Loli, P.16
Iacobone, M.17
Rossi, G.P.18
Biondi, B.19
Lima-Junior, J.V.20
Kater, C.E.21
Bex, M.22
Vikkula, M.23
Grossman, A.B.24
Gruber, S.B.25
Barontini, M.26
Persu, A.27
Castellano, M.28
Toledo, S.P.29
Maher, E.R.30
Mannelli, M.31
Opocher, G.32
Robledo, M.33
Dahia, P.L.34
more..
-
35
-
-
79959752614
-
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
-
Comino-Mendez I, Gracia-Aznarez FJ, Schiavi F, Landa I, Leandro-Garcia LJ, Leton R, Honrado E, Ramos-Medina R, Caronia D, Pita G, Gomez-Grana A, de Cubas AA, Inglada-Perez L, Maliszewska A, Taschin E, Bobisse S, Pica G, Loli P, Hernandez-Lavado R, Diaz JA, Gomez-Morales M, Gonzalez-Neira A, Roncador G, Rodriguez-Antona C, Benitez J, Mannelli M, Opocher G, Robledo M, Cascon A. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma. Nat Genet 2011;43:663-7.
-
(2011)
Nat Genet
, vol.43
, pp. 663-667
-
-
Comino-Mendez, I.1
Gracia-Aznarez, F.J.2
Schiavi, F.3
Landa, I.4
Leandro-Garcia, L.J.5
Leton, R.6
Honrado, E.7
Ramos-Medina, R.8
Caronia, D.9
Pita, G.10
Gomez-Grana, A.11
de Cubas, A.A.12
Inglada-Perez, L.13
Maliszewska, A.14
Taschin, E.15
Bobisse, S.16
Pica, G.17
Loli, P.18
Hernandez-Lavado, R.19
Diaz, J.A.20
Gomez-Morales, M.21
Gonzalez-Neira, A.22
Roncador, G.23
Rodriguez-Antona, C.24
Benitez, J.25
Mannelli, M.26
Opocher, G.27
Robledo, M.28
Cascon, A.29
more..
-
36
-
-
32544439562
-
Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?
-
Cascon A, Montero-Conde C, Ruiz-Llorente S, Mercadillo F, Leton R, Rodriguez-Antona C, Martinez-Delgado B, Delgado M, Diez A, Rovira A, Diaz JA, Robledo M. Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?. Genes Chromosomes Cancer 2006;45:213-19.
-
(2006)
Genes Chromosomes Cancer
, vol.45
, pp. 213-219
-
-
Cascon, A.1
Montero-Conde, C.2
Ruiz-Llorente, S.3
Mercadillo, F.4
Leton, R.5
Rodriguez-Antona, C.6
Martinez-Delgado, B.7
Delgado, M.8
Diez, A.9
Rovira, A.10
Diaz, J.A.11
Robledo, M.12
-
37
-
-
81855183779
-
Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1
-
Pasmant E, Sabbagh A, Masliah-Planchon J, Ortonne N, Laurendeau I, Melin L, Ferkal S, Hernandez L, Leroy K, Valeyrie-Allanore L, Parfait B, Vidaud D, Bieche I, Lantieri L, Wolkenstein P, Vidaud M. Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1. J Natl Cancer Inst 2011;103:1713-22.
-
(2011)
J Natl Cancer Inst
, vol.103
, pp. 1713-1722
-
-
Pasmant, E.1
Sabbagh, A.2
Masliah-Planchon, J.3
Ortonne, N.4
Laurendeau, I.5
Melin, L.6
Ferkal, S.7
Hernandez, L.8
Leroy, K.9
Valeyrie-Allanore, L.10
Parfait, B.11
Vidaud, D.12
Bieche, I.13
Lantieri, L.14
Wolkenstein, P.15
Vidaud, M.16
-
39
-
-
84860740500
-
TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma
-
Abermil N, Guillaud-Bataille M, Burnichon N, Venisse A, Manivet P, Guignat L, Drui D, Chupin M, Josseaume C, Affres H, Plouin PF, Bertherat J, Jeunemaitre X, Gimenez-Roqueplo AP. TMEM127 screening in a large cohort of patients with pheochromocytoma and/or paraganglioma. J Clin Endocrinol Metab 2012;97:E805-9.
-
(2012)
J Clin Endocrinol Metab
, vol.97
, pp. E805-E809
-
-
Abermil, N.1
Guillaud-Bataille, M.2
Burnichon, N.3
Venisse, A.4
Manivet, P.5
Guignat, L.6
Drui, D.7
Chupin, M.8
Josseaume, C.9
Affres, H.10
Plouin, P.F.11
Bertherat, J.12
Jeunemaitre, X.13
Gimenez-Roqueplo, A.P.14
-
40
-
-
77950342008
-
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma
-
Bayley JP, Kunst HP, Cascon A, Sampietro ML, Gaal J, Korpershoek E, Hinojar-Gutierrez A, Timmers HJ, Hoefsloot LH, Hermsen MA, Suarez C, Hussain AK, Vriends AH, Hes FJ, Jansen JC, Tops CM, Corssmit EP, de Knijff P, Lenders JW, Cremers CW, Devilee P, Dinjens WN, de Krijger RR, Robledo M. SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma. Lancet Oncol 2010;11:366-72.
-
(2010)
Lancet Oncol
, vol.11
, pp. 366-372
-
-
Bayley, J.P.1
Kunst, H.P.2
Cascon, A.3
Sampietro, M.L.4
Gaal, J.5
Korpershoek, E.6
Hinojar-Gutierrez, A.7
Timmers, H.J.8
Hoefsloot, L.H.9
Hermsen, M.A.10
Suarez, C.11
Hussain, A.K.12
Vriends, A.H.13
Hes, F.J.14
Jansen, J.C.15
Tops, C.M.16
Corssmit, E.P.17
de Knijff, P.18
Lenders, J.W.19
Cremers, C.W.20
Devilee, P.21
Dinjens, W.N.22
de Krijger, R.R.23
Robledo, M.24
more..
-
41
-
-
84897524498
-
Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas
-
Castro-Vega LJ, Buffet A, De Cubas AA, Cascon A, Menara M, Khalifa E, Amar L, Azriel S, Bourdeau I, Chabre O, Curras-Freixes M, Franco-Vidal V, Guillaud-Bataille M, Simian C, Morin A, Leton R, Gomez-Grana A, Pollard PJ, Rustin P, Robledo M, Favier J, Gimenez-Roqueplo AP. Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas. Hum Mol Genet 2014;23:2440-6.
-
(2014)
Hum Mol Genet
, vol.23
, pp. 2440-2446
-
-
Castro-Vega, L.J.1
Buffet, A.2
De Cubas, A.A.3
Cascon, A.4
Menara, M.5
Khalifa, E.6
Amar, L.7
Azriel, S.8
Bourdeau, I.9
Chabre, O.10
Curras-Freixes, M.11
Franco-Vidal, V.12
Guillaud-Bataille, M.13
Simian, C.14
Morin, A.15
Leton, R.16
Gomez-Grana, A.17
Pollard, P.J.18
Rustin, P.19
Robledo, M.20
Favier, J.21
Gimenez-Roqueplo, A.P.22
more..
-
42
-
-
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. Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 2000;60:6822-5.
-
(2000)
Cancer Res
, vol.60
, pp. 6822-6825
-
-
Gimm, O.1
Armanios, M.2
Dziema, H.3
Neumann, H.P.4
Eng, C.5
-
43
-
-
33747638645
-
Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?
-
Jimenez C, Cote G, Arnold A, Gagel RF. Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? J Clin Endocrinol Metab 2006;91:2851-8.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 2851-2858
-
-
Jimenez, C.1
Cote, G.2
Arnold, A.3
Gagel, R.F.4
-
44
-
-
84877906693
-
Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis
-
Comino-Mendez I, de Cubas AA, Bernal C, Alvarez-Escola C, Sanchez-Malo C, Ramirez-Tortosa CL, Pedrinaci S, Rapizzi E, Ercolino T, Bernini G, Bacca A, Leton R, Pita G, Alonso MR, Leandro-Garcia LJ, Gomez-Grana A, Inglada-Perez L, Mancikova V, Rodriguez-Antona C, Mannelli M, Robledo M, Cascon A. Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis. Hum Mol Genet 2013;22:2169-76.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 2169-2176
-
-
Comino-Mendez, I.1
de Cubas, A.A.2
Bernal, C.3
Alvarez-Escola, C.4
Sanchez-Malo, C.5
Ramirez-Tortosa, C.L.6
Pedrinaci, S.7
Rapizzi, E.8
Ercolino, T.9
Bernini, G.10
Bacca, A.11
Leton, R.12
Pita, G.13
Alonso, M.R.14
Leandro-Garcia, L.J.15
Gomez-Grana, A.16
Inglada-Perez, L.17
Mancikova, V.18
Rodriguez-Antona, C.19
Mannelli, M.20
Robledo, M.21
Cascon, A.22
more..
-
45
-
-
84922567353
-
Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma
-
Sue M, Martucci V, Frey F, Lenders J, Timmers HJ, Peczkowska M, Prejbisz A, Swantje B, Bornstein SR, Arlt W, Fassnacht M, Beuschlein F, Robledo M, Pacak K, Eisenhofer G. Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma. Eur J Endocrinol 2015;172:89-95.
-
(2015)
Eur J Endocrinol
, vol.172
, pp. 89-95
-
-
Sue, M.1
Martucci, V.2
Frey, F.3
Lenders, J.4
Timmers, H.J.5
Peczkowska, M.6
Prejbisz, A.7
Swantje, B.8
Bornstein, S.R.9
Arlt, W.10
Fassnacht, M.11
Beuschlein, F.12
Robledo, M.13
Pacak, K.14
Eisenhofer, G.15
-
46
-
-
84879922746
-
The genetic landscape of pheochromocytomas and paragangliomas: somatic mutations take center stage
-
Dahia PL. The genetic landscape of pheochromocytomas and paragangliomas: somatic mutations take center stage. J Clin Endocrinol Metab 2013;98:2679-81.
-
(2013)
J Clin Endocrinol Metab
, vol.98
, pp. 2679-2681
-
-
Dahia, P.L.1
-
48
-
-
84893813840
-
Mosaicism in HIF2A-related polycythemia-paraganglioma syndrome
-
Buffet A, Smati S, Mansuy L, Menara M, Lebras M, Heymann MF, Simian C, Favier J, Murat A, Cariou B, Gimenez-Roqueplo AP. Mosaicism in HIF2A-related polycythemia-paraganglioma syndrome. J Clin Endocrinol Metab 2014;99:E369-73.
-
(2014)
J Clin Endocrinol Metab
, vol.99
, pp. E369-E373
-
-
Buffet, A.1
Smati, S.2
Mansuy, L.3
Menara, M.4
Lebras, M.5
Heymann, M.F.6
Simian, C.7
Favier, J.8
Murat, A.9
Cariou, B.10
Gimenez-Roqueplo, A.P.11
-
49
-
-
84879606718
-
A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma
-
Lorenzo FR, Yang C, Ng Tang Fui M, Vankayalapati H, Zhuang Z, Huynh T, Grossmann M, Pacak K, Prchal JT. A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma. J Mol Med (Berl) 2013;91:507-12.
-
(2013)
J Mol Med (Berl)
, vol.91
, pp. 507-512
-
-
Lorenzo, F.R.1
Yang, C.2
Ng Tang Fui, M.3
Vankayalapati, H.4
Zhuang, Z.5
Huynh, T.6
Grossmann, M.7
Pacak, K.8
Prchal, J.T.9
-
50
-
-
84893617173
-
Long-term prognosis of patients with pediatric pheochromocytoma
-
Bausch B, Wellner U, Bausch D, Schiavi F, Barontini M, Sanso G, Walz MK, Peczkowska M, Weryha G, Dall'igna P, Cecchetto G, Bisogno G, Moeller LC, Bockenhauer D, Patocs A, Racz K, Zabolotnyi D, Yaremchuk S, Dzivite-Krisane I, Castinetti F, Taieb D, Malinoc A, von Dobschuetz E, Roessler J, Schmid KW, Opocher G, Eng C, Neumann HP. Long-term prognosis of patients with pediatric pheochromocytoma. Endocr Relat Cancer 2014;21:17-25.
-
(2014)
Endocr Relat Cancer
, vol.21
, pp. 17-25
-
-
Bausch, B.1
Wellner, U.2
Bausch, D.3
Schiavi, F.4
Barontini, M.5
Sanso, G.6
Walz, M.K.7
Peczkowska, M.8
Weryha, G.9
Dall'igna, P.10
Cecchetto, G.11
Bisogno, G.12
Moeller, L.C.13
Bockenhauer, D.14
Patocs, A.15
Racz, K.16
Zabolotnyi, D.17
Yaremchuk, S.18
Dzivite-Krisane, I.19
Castinetti, F.20
Taieb, D.21
Malinoc, A.22
von Dobschuetz, E.23
Roessler, J.24
Schmid, K.W.25
Opocher, G.26
Eng, C.27
Neumann, H.P.28
more..
-
51
-
-
84879493954
-
Genetics of pheochromocytoma and paraganglioma in Spanish pediatric patients
-
Cascon A, Inglada-Perez L, Comino-Mendez I, de Cubas AA, Leton R, Mora J, Marazuela M, Galofre JC, Quesada-Charneco M, Robledo M. Genetics of pheochromocytoma and paraganglioma in Spanish pediatric patients. Endocr Relat Cancer 2013;20:L1-6.
-
(2013)
Endocr Relat Cancer
, vol.20
, pp. L1-6
-
-
Cascon, A.1
Inglada-Perez, L.2
Comino-Mendez, I.3
de Cubas, A.A.4
Leton, R.5
Mora, J.6
Marazuela, M.7
Galofre, J.C.8
Quesada-Charneco, M.9
Robledo, M.10
-
52
-
-
84865694593
-
Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia
-
Zhuang Z, Yang C, Lorenzo F, Merino M, Fojo T, Kebebew E, Popovic V, Stratakis CA, Prchal JT, Pacak K. Somatic HIF2A gain-of-function mutations in paraganglioma with polycythemia. N Engl J Med 2012;367:922-30.
-
(2012)
N Engl J Med
, vol.367
, pp. 922-930
-
-
Zhuang, Z.1
Yang, C.2
Lorenzo, F.3
Merino, M.4
Fojo, T.5
Kebebew, E.6
Popovic, V.7
Stratakis, C.A.8
Prchal, J.T.9
Pacak, K.10
-
53
-
-
84870022554
-
HIF2A mutations in paraganglioma with polycythemia
-
author reply-2
-
Favier J, Buffet A, Gimenez-Roqueplo AP. HIF2A mutations in paraganglioma with polycythemia. N Engl J Med 2012;367:2161; author reply-2.
-
(2012)
N Engl J Med
, vol.367
, pp. 2161
-
-
Favier, J.1
Buffet, A.2
Gimenez-Roqueplo, A.P.3
-
54
-
-
0141704510
-
Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas
-
Gimenez-Roqueplo AP, Favier J, Rustin P, Rieubland C, Crespin M, Nau V, Khau Van Kien P, Corvol P, Plouin PF, Jeunemaitre X. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res 2003;63:5615-21.
-
(2003)
Cancer Res
, vol.63
, pp. 5615-5621
-
-
Gimenez-Roqueplo, A.P.1
Favier, J.2
Rustin, P.3
Rieubland, C.4
Crespin, M.5
Nau, V.6
Khau Van Kien, P.7
Corvol, P.8
Plouin, P.F.9
Jeunemaitre, X.10
-
55
-
-
0029864134
-
Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility
-
Adopted on February 20 1996
-
[No authors listed]. Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996. J Clin Oncol 1996;14:1730-6; discussion 7-40.
-
(1996)
J., Clin Oncol
, vol.14
, pp. 1730-1736
-
-
-
56
-
-
84880077252
-
Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing
-
Fishbein L, Merrill S, Fraker DL, Cohen DL, Nathanson KL. Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. Ann Surg Oncol 2013;20:1444-50.
-
(2013)
Ann Surg Oncol
, vol.20
, pp. 1444-1450
-
-
Fishbein, L.1
Merrill, S.2
Fraker, D.L.3
Cohen, D.L.4
Nathanson, K.L.5
-
57
-
-
82755182455
-
Is genetic screening indicated in apparently sporadic pheochromocytomas and paragangliomas?
-
Iacobone M, Schiavi F, Bottussi M, Taschin E, Bobisse S, Fassina A, Opocher G, Favia G. Is genetic screening indicated in apparently sporadic pheochromocytomas and paragangliomas? Surgery 2011;150:1194-201.
-
(2011)
Surgery
, vol.150
, pp. 1194-1201
-
-
Iacobone, M.1
Schiavi, F.2
Bottussi, M.3
Taschin, E.4
Bobisse, S.5
Fassina, A.6
Opocher, G.7
Favia, G.8
|