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Items: 1 to 20 of 110

1.

Genetic aspects of pheochromocytoma.

Kolačkov K, Tupikowski K, Bednarek-Tupikowska G.

Adv Clin Exp Med. 2012 Nov-Dec;21(6):821-9. Review.

2.

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.

3.

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
4.

[Genetic tests in oncology practice with emphasis on the RET oncogene and VHL tumor suppressor gene].

Nesković G, Stanojević B, Palmar I, Dimitrijević B.

Srp Arh Celok Lek. 2002 Jul;130 Suppl 2:52-7. Serbian.

PMID:
12584999
5.

Denaturing high performance liquid chromatography detection of SDHB, SDHD, and VHL germline mutations in pheochromocytoma.

Meyer-Rochow GY, Smith JM, Richardson AL, Marsh DJ, Sidhu SB, Robinson BG, Benn DE.

J Surg Res. 2009 Nov;157(1):55-62. doi: 10.1016/j.jss.2008.07.043. Epub 2008 Sep 4.

PMID:
19215943
6.

[Genetics of pheochromocytoma].

Bausch B, Malinoc A, Maruschke L, Offergeld C, Gläsker S, Rischke HC, Brauckhoff M, Boedeker CC, Neumann HP.

Chirurg. 2012 Jun;83(6):511-8. doi: 10.1007/s00104-011-2191-8. Review. German.

PMID:
22481546
7.

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
8.

Genetics of pheochromocytomas and paragangliomas.

Opocher G, Schiavi F.

Best Pract Res Clin Endocrinol Metab. 2010 Dec;24(6):943-56. doi: 10.1016/j.beem.2010.05.001. Review.

PMID:
21115163
9.

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.

10.

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.

11.

Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas.

Krawczyk A, Hasse-Lazar K, Pawlaczek A, Szpak-Ulczok S, Krajewska J, Paliczka-Cieślak E, Jurecka-Lubieniecka B, Roskosz J, Chmielik E, Ziaja J, Cierpka L, Peczkowska M, Preibisz A, Januszewicz A, Otto M, Jarzab B.

Endokrynol Pol. 2010 Jan-Feb;61(1):43-8.

12.

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
13.

Candidate gene mutation analysis in bilateral adrenal pheochromocytoma and sympathetic paraganglioma.

Korpershoek E, Petri BJ, van Nederveen FH, Dinjens WN, Verhofstad AA, de Herder WW, Schmid S, Perren A, Komminoth P, de Krijger RR.

Endocr Relat Cancer. 2007 Jun;14(2):453-62.

14.

Genetic testing in pheochromocytoma: increasing importance for clinical decision making.

Bornstein SR, Gimenez-Roqueplo AP.

Ann N Y Acad Sci. 2006 Aug;1073:94-103.

PMID:
17102076
15.

Frequent genetic changes in childhood pheochromocytomas.

De Krijger RR, Petri BJ, Van Nederveen FH, Korpershoek E, De Herder WW, De Muinck Keizer-Schrama SM, Dinjens WN.

Ann N Y Acad Sci. 2006 Aug;1073:166-76. Erratum in: Ann N Y Acad Sci. 2006;1086:241. Petri, Bart-Jeroen [added].

PMID:
17102083
16.

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
17.
18.

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
19.

[Hereditary pheochromocytoma and paraganglioma].

Musil Z, Vícha A, Zelinka T, Turková H, Labudová T, Kohoutová M, Pacák K.

Klin Onkol. 2012;25 Suppl:S21-6. Czech.

PMID:
22920202
20.

Familial pheochromocytoma.

Erlic Z, Neumann HP.

Hormones (Athens). 2009 Jan-Mar;8(1):29-38.

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