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Items: 1 to 20 of 71

1.

Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience.

Korpershoek E, Van Nederveen FH, Dannenberg H, Petri BJ, Komminoth P, Perren A, Lenders JW, Verhofstad AA, De Herder WW, De Krijger RR, Dinjens WN.

Ann N Y Acad Sci. 2006 Aug;1073:138-48.

PMID:
17102080
2.

Pheochromocytoma in von Hippel-Lindau disease and neurofibromatosis type 1.

Opocher G, Conton P, Schiavi F, Macino B, Mantero F.

Fam Cancer. 2005;4(1):13-6. Review.

PMID:
15883705
3.

Pheochromocytoma: the expanding genetic differential diagnosis.

Bryant J, Farmer J, Kessler LJ, Townsend RR, Nathanson KL.

J Natl Cancer Inst. 2003 Aug 20;95(16):1196-204. Review.

4.

Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.

Fishbein L, Nathanson KL.

Cancer Genet. 2012 Jan-Feb;205(1-2):1-11. doi: 10.1016/j.cancergen.2012.01.009. Review.

5.

[Genetics of paragangliomas and pheochromocytomas].

Favier J, Gimenez-Roqueplo AP.

Med Sci (Paris). 2012 Jun-Jul;28(6-7):625-32. doi: 10.1051/medsci/2012286016. Epub 2012 Jul 16. Review. French.

6.

New insights into the genetics of familial chromaffin cell tumors.

Koch CA, Vortmeyer AO, Zhuang Z, Brouwers FM, Pacak K.

Ann N Y Acad Sci. 2002 Sep;970:11-28. Review.

PMID:
12381538
7.

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

Welander J, Söderkvist P, Gimm O.

Endocr Relat Cancer. 2011 Dec 1;18(6):R253-76. doi: 10.1530/ERC-11-0170. Print 2011 Dec. Review.

8.
9.

Genetics and molecular pathogenesis of pheochromocytoma and paraganglioma.

Galan SR, Kann PH.

Clin Endocrinol (Oxf). 2013 Feb;78(2):165-75. doi: 10.1111/cen.12071. Review.

PMID:
23061808
10.

Review: Should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes?

Jiménez C, Cote G, Arnold A, Gagel RF.

J Clin Endocrinol Metab. 2006 Aug;91(8):2851-8. Epub 2006 May 30. Review.

PMID:
16735498
11.

Transcription association of VHL and SDH mutations link hypoxia and oxidoreductase signals in pheochromocytomas.

Dahia PL; Familial Pheochromocytoma Consortium.

Ann N Y Acad Sci. 2006 Aug;1073:208-20. Review.

PMID:
17102089
12.

[Hereditary paragangliomas and pheochromocytomas].

Gimenez-Roqueplo AP.

Nephrol Ther. 2006 Jan;2 Suppl 2:S137-42. Review. French.

PMID:
17373214
13.

Pheochromocytoma and functional paraganglioma syndrome: no longer the 10% tumor.

Elder EE, Elder G, Larsson C.

J Surg Oncol. 2005 Mar 1;89(3):193-201. Review.

PMID:
15719371
14.

Pheochromocytoma: an update on genetics and management.

Karagiannis A, Mikhailidis DP, Athyros VG, Harsoulis F.

Endocr Relat Cancer. 2007 Dec;14(4):935-56. Review.

15.

The pressure rises: update on the genetics of phaeochromocytoma.

Maher ER, Eng C.

Hum Mol Genet. 2002 Oct 1;11(20):2347-54. Review.

16.

Genetic testing in pheochromocytoma- and paraganglioma-associated syndromes.

Benn DE, Richardson AL, Marsh DJ, Robinson BG.

Ann N Y Acad Sci. 2006 Aug;1073:104-11. Review.

PMID:
17102077
17.

An update on the genetics of paraganglioma, pheochromocytoma, and associated hereditary syndromes.

Gimenez-Roqueplo AP, Dahia PL, Robledo M.

Horm Metab Res. 2012 May;44(5):328-33. doi: 10.1055/s-0031-1301302. Epub 2012 Feb 10. Review.

PMID:
22328163
18.

New insights in the genetics of adrenocortical tumors, pheochromocytomas and paragangliomas.

Bertherat J, Gimenez-Roqueplo AP.

Horm Metab Res. 2005 Jun;37(6):384-90. Review.

PMID:
16001332
19.

Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.

Boedeker CC, Erlic Z, Richard S, Kontny U, Gimenez-Roqueplo AP, Cascon A, Robledo M, de Campos JM, van Nederveen FH, de Krijger RR, Burnichon N, Gaal J, Walter MA, Reschke K, Wiech T, Weber J, Rückauer K, Plouin PF, Darrouzet V, Giraud S, Eng C, Neumann HP.

J Clin Endocrinol Metab. 2009 Jun;94(6):1938-44. doi: 10.1210/jc.2009-0354. Epub 2009 Mar 31. Review.

20.

Molecular genetic alterations in adrenal and extra-adrenal pheochromocytomas and paragangliomas.

Dannenberg H, Komminoth P, Dinjens WN, Speel EJ, de Krijger RR.

Endocr Pathol. 2003 Winter;14(4):329-50. Review.

PMID:
14739490
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