410 related articles for article (PubMed ID: 10458336)
1. Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma.
Walther MM; Reiter R; Keiser HR; Choyke PL; Venzon D; Hurley K; Gnarra JR; Reynolds JC; Glenn GM; Zbar B; Linehan WM
J Urol; 1999 Sep; 162(3 Pt 1):659-64. PubMed ID: 10458336
[TBL] [Abstract][Full Text] [Related]
2. Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease.
Neumann HP; Berger DP; Sigmund G; Blum U; Schmidt D; Parmer RJ; Volk B; Kirste G
N Engl J Med; 1993 Nov; 329(21):1531-8. PubMed ID: 8105382
[TBL] [Abstract][Full Text] [Related]
3. Management of hereditary pheochromocytoma in von Hippel-Lindau kindreds with partial adrenalectomy.
Walther MM; Keiser HR; Choyke PL; Rayford W; Lyne JC; Linehan WM
J Urol; 1999 Feb; 161(2):395-8. PubMed ID: 9915410
[TBL] [Abstract][Full Text] [Related]
4. Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
Gergics P; Patocs A; Toth M; Igaz P; Szucs N; Liko I; Fazakas F; Szabo I; Kovacs B; Glaz E; Racz K
Eur J Endocrinol; 2009 Sep; 161(3):495-502. PubMed ID: 19574279
[TBL] [Abstract][Full Text] [Related]
5. Three-decade investigation of familial pheochromocytoma. An allele of von Hippel-Lindau disease?
Tisherman SE; Tisherman BG; Tisherman SA; Dunmire S; Levey GS; Mulvihill JJ
Arch Intern Med; 1993 Nov; 153(22):2550-6. PubMed ID: 8239848
[TBL] [Abstract][Full Text] [Related]
6. Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
Eisenhofer G; Lenders JW; Linehan WM; Walther MM; Goldstein DS; Keiser HR
N Engl J Med; 1999 Jun; 340(24):1872-9. PubMed ID: 10369850
[TBL] [Abstract][Full Text] [Related]
7. [Pheochromocytoma in Von Hippel Lindau disease. 3 cases].
Tourniaire J; Pradat P; Chalendar D
Ann Endocrinol (Paris); 1995; 56(6):609-12. PubMed ID: 8787353
[TBL] [Abstract][Full Text] [Related]
8. Distinct gene expression profiles in norepinephrine- and epinephrine-producing hereditary and sporadic pheochromocytomas: activation of hypoxia-driven angiogenic pathways in von Hippel-Lindau syndrome.
Eisenhofer G; Huynh TT; Pacak K; Brouwers FM; Walther MM; Linehan WM; Munson PJ; Mannelli M; Goldstein DS; Elkahloun AG
Endocr Relat Cancer; 2004 Dec; 11(4):897-911. PubMed ID: 15613462
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Von Hippel-Lindau disease and rapidly progressing pheochromocytomas in siblings.
Fugaru I; Goudie C; Capolicchio JP
Fam Cancer; 2022 Apr; 21(2):229-233. PubMed ID: 33877494
[TBL] [Abstract][Full Text] [Related]
11. Intrathoracic and multiple abdominal pheochromocytomas in von Hippel-Lindau disease.
Hoffman RW; Gardner DW; Mitchell FL
Arch Intern Med; 1982 Oct; 142(10):1962-4. PubMed ID: 7125783
[TBL] [Abstract][Full Text] [Related]
12. Use of the tyrosine kinase inhibitor sunitinib in a patient with von Hippel-Lindau disease: targeting angiogenic factors in pheochromocytoma and other von Hippel-Lindau disease-related tumors.
Jimenez C; Cabanillas ME; Santarpia L; Jonasch E; Kyle KL; Lano EA; Matin SF; Nunez RF; Perrier ND; Phan A; Rich TA; Shah B; Williams MD; Waguespack SG
J Clin Endocrinol Metab; 2009 Feb; 94(2):386-91. PubMed ID: 19017755
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Biochemically normal adrenal pheochromocytoma following extensive central necrosis in a child with von Hippel-Lindau (VHL) gene mutation.
Ng BW; Wong JS; Toh TH
BMJ Case Rep; 2021 Dec; 14(12):. PubMed ID: 34937752
[TBL] [Abstract][Full Text] [Related]
15. A novel von Hippel-Lindau point mutation presents as apparently sporadic pheochromocytoma.
Rich TA; Jonasch E; Matin S; Waguespack SG; Gombos DS; Santarpia L; Stolle C; Jimenez C
Cancer Invest; 2008 Jul; 26(6):642-6. PubMed ID: 18584357
[TBL] [Abstract][Full Text] [Related]
16. Phaeochromocytoma associated with a de novo VHL mutation as form fruste of von Hippel-Lindau disease.
Frenzel S; Apel TW; Heidemann PH; Zerres K; Neumann HP; Dörr HG
Eur J Pediatr; 2001 Jul; 160(7):421-4. PubMed ID: 11475579
[TBL] [Abstract][Full Text] [Related]
17. Pheochromocytoma and Von Hippel-Lindau in pregnancy.
Kolomeyevskaya N; Blazo M; Van den Veyver I; Strehlow S; Aagaard-Tillery KM
Am J Perinatol; 2010 Mar; 27(3):257-63. PubMed ID: 19784914
[TBL] [Abstract][Full Text] [Related]
18. Early identification of patients with von Hippel-Lindau disease at risk for pheochromocytoma.
Maranchie JK; Walther MM
Curr Urol Rep; 2001 Feb; 2(1):24-30. PubMed ID: 12084291
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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. PubMed ID: 15883705
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
