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Items: 1 to 20 of 96

1.

Pheochromocytoma: implications in tumorigenesis and the actual management.

Shah U, Giubellino A, Pacak K.

Minerva Endocrinol. 2012 Jun;37(2):141-56. Review.

2.

[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. Review. French.

3.

[Malignant pheochromocytoma].

Tanabe A, Tsuiki M, Takano K, Naruse M.

Nihon Rinsho. 2006 May 28;Suppl 1:739-43. Review. Japanese. No abstract available.

PMID:
16776263
4.

[Pheochromocytoma].

Arai H, Nakao K.

Nihon Rinsho. 2006 May 28;Suppl 1:724-9. Review. Japanese. No abstract available.

PMID:
16776260
5.

Pheochromocytomas and secreting paragangliomas.

Plouin PF, Gimenez-Roqueplo AP.

Orphanet J Rare Dis. 2006 Dec 8;1:49. Review.

6.

Pheochromocytoma.

Eigelberger MS, Duh QY.

Curr Treat Options Oncol. 2001 Aug;2(4):321-9. Review.

PMID:
12057112
7.

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.

J Clin Oncol. 2005 Dec 1;23(34):8812-8.

PMID:
16314641
8.

Risk-oriented approach to hereditary adrenal pheochromocytoma.

Machens A, Brauckhoff M, Gimm O, Dralle H.

Ann N Y Acad Sci. 2006 Aug;1073:417-28.

PMID:
17102110
9.

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
10.

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.

PMID:
12928344
11.

[Familial pheochromocytoma].

Tamura N, Nakao K.

Nihon Rinsho. 2006 May 28;Suppl 1:730-4. Review. Japanese. No abstract available.

PMID:
16776261
12.

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
13.

Phaeochromocytoma in children.

Armstrong R, Sridhar M, Greenhalgh KL, Howell L, Jones C, Landes C, McPartland JL, Moores C, Losty PD, Didi M.

Arch Dis Child. 2008 Oct;93(10):899-904. doi: 10.1136/adc.2008.139121. Review.

PMID:
18499773
14.

Diagnosis and management of pheochromocytoma.

Kenady DE, McGrath PC, Sloan DA, Schwartz RW.

Curr Opin Oncol. 1997 Jan;9(1):61-7. Review.

PMID:
9090495
15.

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
16.

Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing.

Fishbein L, Merrill S, Fraker DL, Cohen DL, Nathanson KL.

Ann Surg Oncol. 2013 May;20(5):1444-50. doi: 10.1245/s10434-013-2942-5.

17.

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.

J Clin Endocrinol Metab. 2013 Jul;98(7):E1248-56. doi: 10.1210/jc.2013-1319.

PMID:
23666964
18.

Hereditary pheochromocytoma and paraganglioma.

Mazzaglia PJ.

J Surg Oncol. 2012 Oct 1;106(5):580-5. doi: 10.1002/jso.23157. Review.

PMID:
22648936
19.

Endocrine manifestations of von Hippel-Lindau disease.

Cassol C, Mete O.

Arch Pathol Lab Med. 2015 Feb;139(2):263-8. doi: 10.5858/arpa.2013-0520-RS. Review.

PMID:
25611110
20.

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.

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