-
1
-
-
0027395614
-
Familial risk for neuroendocrine tumors
-
Anderson RJ, Lynch HT. 1993. Familial risk for neuroendocrine tumors. Curr Opin Oncol 5:75-84.
-
(1993)
Curr Opin Oncol
, vol.5
, pp. 75-84
-
-
Anderson, R.J.1
Lynch, H.T.2
-
2
-
-
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
-
3
-
-
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 CW 3rd, 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
-
4
-
-
4444356015
-
An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma
-
Baysal BE, Willett-Brozick JE, Filho PA, Lawrence EC, Myers EN, Ferrell RE. 2004. An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma. J Med Genet 41:703-709.
-
(2004)
J Med Genet
, vol.41
, pp. 703-709
-
-
Baysal, B.E.1
Willett-Brozick, J.E.2
Filho, P.A.3
Lawrence, E.C.4
Myers, E.N.5
Ferrell, R.E.6
-
5
-
-
6044230918
-
Molecular profiling of inflammatory breast cancer: Identification of a poor-prognosis gene expression signature
-
Bieche I, Lerebours F, Tozlu S, Espie M, Marty M, Lidereau R. 2004. Molecular profiling of inflammatory breast cancer: identification of a poor-prognosis gene expression signature. Clin Cancer Res 10:6789-6795.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 6789-6795
-
-
Bieche, I.1
Lerebours, F.2
Tozlu, S.3
Espie, M.4
Marty, M.5
Lidereau, R.6
-
6
-
-
15744369194
-
Clinical characteristics of pheochromocytoma patients with germ-line mutations in SDHD
-
Dannenberg H, van Nederveen FH, Abbou M, Verhofstad AA, Komminoth P, de Krijger RR, Dinjens WN. 2005. Clinical characteristics of pheochromocytoma patients with germ-line mutations in SDHD. J Clin Oncol 23:1894-1901.
-
(2005)
J Clin Oncol
, vol.23
, pp. 1894-1901
-
-
Dannenberg, H.1
Van Nederveen, F.H.2
Abbou, M.3
Verhofstad, A.A.4
Komminoth, P.5
De Krijger, R.R.6
Dinjens, W.N.7
-
7
-
-
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. 2003. Mutations in the SDHB gene are associated with extra-adrenal and/or malignant phaeochromocytomas. Cancer Res 63:5615-5621.
-
(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
-
8
-
-
0036778597
-
The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors
-
Kolomietz E, Meyn MS, Pandita A, Squire JA. 2002. The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors. Genes Chromosomes Cancer 35:97-112.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 97-112
-
-
Kolomietz, E.1
Meyn, M.S.2
Pandita, A.3
Squire, J.A.4
-
10
-
-
0029940856
-
Phenotypic expression in von Hippel-Lindau disease: Correlations with germ-line VHL gene mutations
-
Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT. 1996. Phenotypic expression in von Hippel-Lindau disease: correlations with germ-line VHL gene mutations. J Med Genet 33:328-332.
-
(1996)
J Med Genet
, vol.33
, pp. 328-332
-
-
Maher, E.R.1
Webster, A.R.2
Richards, F.M.3
Green, J.S.4
Crossey, P.A.5
Payne, S.J.6
Moore, A.T.7
-
11
-
-
8744288709
-
Large germ-line deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma
-
McWhinney SR, Pilarski RT, Forrester SR, Schneider MC, Sarquis MM, Dias EP, Eng C. 2004. Large germ-line deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma. J Clin Endocrinol Metab 89:5694-5699.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 5694-5699
-
-
McWhinney, S.R.1
Pilarski, R.T.2
Forrester, S.R.3
Schneider, M.C.4
Sarquis, M.M.5
Dias, E.P.6
Eng, C.7
-
12
-
-
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. 2002. Germ-line mutations in nonsyndromic pheochromocytoma. N Engl J Med 346:1459-1466.
-
(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..
-
13
-
-
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
-
14
-
-
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
-
16
-
-
0025081167
-
Multiple endocrine neoplasia: How many syndromes?
-
Schimke RN. 1990. Multiple endocrine neoplasia: how many syndromes? Am J Med Genet 37:375-383.
-
(1990)
Am J Med Genet
, vol.37
, pp. 375-383
-
-
Schimke, R.N.1
-
17
-
-
3543023204
-
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification
-
Schonten JP, McElgunn CJ, Waaijer R, Zwijnenburg D, Diepvens F, Pals G. 2002. Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification. Nucleic Acids Res 30:e57.
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Schonten, J.P.1
McElgunn, C.J.2
Waaijer, R.3
Zwijnenburg, D.4
Diepvens, F.5
Pals, G.6
-
18
-
-
9144249602
-
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma
-
Vanharanta S, Buchta M, McWhinney SR, Virta SK, Peczkowska M, Morrison CD, Lehtonen R, Januszewicz A, Jarvinen H, Juhola M, Mecklin JP, Pukkala E, Herva R, Kiuru M, Nupponen NN, Aaltonen LA, Neumann HP, Eng C. 2004. Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. Am J Hum Genet 74:153-159.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 153-159
-
-
Vanharanta, S.1
Buchta, M.2
McWhinney, S.R.3
Virta, S.K.4
Peczkowska, M.5
Morrison, C.D.6
Lehtonen, R.7
Januszewicz, A.8
Jarvinen, H.9
Juhola, M.10
Mecklin, J.P.11
Pukkala, E.12
Herva, R.13
Kiuru, M.14
Nupponen, N.N.15
Aaltonen, L.A.16
Neumann, H.P.17
Eng, C.18
|