131 related articles for article (PubMed ID: 19153209)
1. Array-comparative genomic hybridization in sporadic benign pheochromocytomas.
van Nederveen FH; Korpershoek E; deLeeuw RJ; Verhofstad AA; Lenders JW; Dinjens WN; Lam WL; de Krijger RR
Endocr Relat Cancer; 2009 Jun; 16(2):505-13. PubMed ID: 19153209
[TBL] [Abstract][Full Text] [Related]
2. Microarray-based CGH of sporadic and syndrome-related pheochromocytomas using a 0.1-0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p.
Aarts M; Dannenberg H; deLeeuw RJ; van Nederveen FH; Verhofstad AA; Lenders JW; Dinjens WN; Speel EJ; Lam WL; de Krijger RR
Genes Chromosomes Cancer; 2006 Jan; 45(1):83-93. PubMed ID: 16215979
[TBL] [Abstract][Full Text] [Related]
3. Differential genetic alterations in von Hippel-Lindau syndrome-associated and sporadic pheochromocytomas.
Bender BU; Gutsche M; Gläsker S; Müller B; Kirste G; Eng C; Neumann HP
J Clin Endocrinol Metab; 2000 Dec; 85(12):4568-74. PubMed ID: 11134110
[TBL] [Abstract][Full Text] [Related]
4. Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.
Opocher G; Schiavi F; Vettori A; Pampinella F; Vitiello L; Calderan A; Vianello B; Murgia A; Martella M; Taccaliti A; Mantero F; Mostacciuolo ML
Clin Endocrinol (Oxf); 2003 Dec; 59(6):707-15. PubMed ID: 14974911
[TBL] [Abstract][Full Text] [Related]
5. Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p.
Benn DE; Dwight T; Richardson AL; Delbridge L; Bambach CP; Stowasser M; Gordon RD; Marsh DJ; Robinson BG
Cancer Res; 2000 Dec; 60(24):7048-51. PubMed ID: 11156410
[TBL] [Abstract][Full Text] [Related]
6. Molecular cytogenetic characterization in four pediatric pheochromocytomas and paragangliomas.
Vicha A; Holzerova M; Krepelova A; Musil Z; Prochazka P; Sumerauer D; Kodet R; Eckschlager T; Jarosova M
Pathol Oncol Res; 2011 Dec; 17(4):801-8. PubMed ID: 21461997
[TBL] [Abstract][Full Text] [Related]
7. Von Hippel-Lindau gene alterations in sporadic benign and malignant pheochromocytomas.
Dannenberg H; De Krijger RR; van der Harst E; Abbou M; IJzendoorn Y; Komminoth P; Dinjens WN
Int J Cancer; 2003 Jun; 105(2):190-5. PubMed ID: 12673678
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 17102080
[TBL] [Abstract][Full Text] [Related]
9. Intra-tumoral molecular heterogeneity in benign and malignant pheochromocytomas and extra-adrenal sympathetic paragangliomas.
Korpershoek E; Stobbe CK; van Nederveen FH; de Krijger RR; Dinjens WN
Endocr Relat Cancer; 2010 Sep; 17(3):653-62. PubMed ID: 20488782
[TBL] [Abstract][Full Text] [Related]
10. Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis.
Sandgren J; Diaz de Ståhl T; Andersson R; Menzel U; Piotrowski A; Nord H; Bäckdahl M; Kiss NB; Brauckhoff M; Komorowski J; Dralle H; Hessman O; Larsson C; Akerström G; Bruder C; Dumanski JP; Westin G
Endocr Relat Cancer; 2010 Sep; 17(3):561-79. PubMed ID: 20410162
[TBL] [Abstract][Full Text] [Related]
11. Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology.
Edström E; Mahlamäki E; Nord B; Kjellman M; Karhu R; Höög A; Goncharov N; Teh BT; Bäckdahl M; Larsson C
Am J Pathol; 2000 Feb; 156(2):651-9. PubMed ID: 10666394
[TBL] [Abstract][Full Text] [Related]
12. Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.
Khosla S; Patel VM; Hay ID; Schaid DJ; Grant CS; van Heerden JA; Thibodeau SN
J Clin Invest; 1991 May; 87(5):1691-9. PubMed ID: 2022740
[TBL] [Abstract][Full Text] [Related]
13. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
Moley JF; Brother MB; Fong CT; White PS; Baylin SB; Nelkin B; Wells SA; Brodeur GM
Cancer Res; 1992 Feb; 52(4):770-4. PubMed ID: 1346584
[TBL] [Abstract][Full Text] [Related]
14. Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.
Jarbo C; Buckley PG; Piotrowski A; Mantripragada KK; Benetkiewicz M; Diaz de Ståhl T; Langford CF; Gregory SG; Dralle H; Gimm O; Bäckdahl M; Geli J; Larsson C; Westin G; Akerström G; Dumanski JP
Int J Cancer; 2006 Mar; 118(5):1159-64. PubMed ID: 16161042
[TBL] [Abstract][Full Text] [Related]
15. Characteristic chromosomal aberrations in sporadic cerebellar hemangioblastomas revealed by comparative genomic hybridization.
Sprenger SH; Gijtenbeek JM; Wesseling P; Sciot R; van Calenbergh F; Lammens M; Jeuken JW
J Neurooncol; 2001 May; 52(3):241-7. PubMed ID: 11519854
[TBL] [Abstract][Full Text] [Related]
16. Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma.
Vargas MP; Zhuang Z; Wang C; Vortmeyer A; Linehan WM; Merino MJ
Hum Pathol; 1997 Apr; 28(4):411-5. PubMed ID: 9104939
[TBL] [Abstract][Full Text] [Related]
17. Analysis of von hippel-lindau mutations with comparative genomic hybridization in sporadic and hereditary hemangioblastomas: possible genetic heterogeneity.
Gijtenbeek JM; Jacobs B; Sprenger SH; Eleveld MJ; van Kessel AG; Kros JM; Sciot R; van Calenbergh F; Wesseling P; Jeuken JW
J Neurosurg; 2002 Oct; 97(4):977-82. PubMed ID: 12405390
[TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 17639058
[TBL] [Abstract][Full Text] [Related]
19. Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma.
Zeiger MA; Zbar B; Keiser H; Linehan WM; Gnarra JR
Genes Chromosomes Cancer; 1995 Jul; 13(3):151-6. PubMed ID: 7669733
[TBL] [Abstract][Full Text] [Related]
20. Adrenal medullary hyperplasia is a precursor lesion for pheochromocytoma in MEN2 syndrome.
Korpershoek E; Petri BJ; Post E; van Eijck CH; Oldenburg RA; Belt EJ; de Herder WW; de Krijger RR; Dinjens WN
Neoplasia; 2014 Oct; 16(10):868-73. PubMed ID: 25379023
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
