1215 related articles for article (PubMed ID: 8105382)
1. 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]
2. 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]
3. Pheochromocytoma as the first manifestation of von Hippel-Lindau disease.
Richard S; Beigelman C; Duclos JM; Fendler JP; Plauchu H; Plouin PF; Resche F; Schlumberger M; Vermesse B; Proye C
Surgery; 1994 Dec; 116(6):1076-81. PubMed ID: 7985090
[TBL] [Abstract][Full Text] [Related]
4. [Pheochromocytoma, first manifestation of Von Hippel-Lindau disease: a possibility to be considered].
Richard S; Resche F; Vermesse B; Fendler JP; Francillard M; Laroche F; Luton JP; Méry JP; Proye C; Redondo A
Arch Mal Coeur Vaiss; 1992 Aug; 85(8):1153-6. PubMed ID: 1482250
[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. 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]
7. Islet cell tumors in von Hippel-Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias.
Binkovitz LA; Johnson CD; Stephens DH
AJR Am J Roentgenol; 1990 Sep; 155(3):501-5. PubMed ID: 1974734
[TBL] [Abstract][Full Text] [Related]
8. Bilateral pheochromocytoma as first manifestation of von Hippel-Lindau disease: a case report.
Catli G; Abaci A; Neumann HC; Altincik A; Demir K; Böber E
Turk J Pediatr; 2012; 54(5):532-5. PubMed ID: 23427520
[TBL] [Abstract][Full Text] [Related]
9. Surgical management of hereditary pheochromocytoma.
Yip L; Lee JE; Shapiro SE; Waguespack SG; Sherman SI; Hoff AO; Gagel RF; Arens JF; Evans DB
J Am Coll Surg; 2004 Apr; 198(4):525-34; discussion 534-5. PubMed ID: 15051000
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [The von Hippel-Lindau syndrome with pheochromocytoma].
Palmar I; Vircburger M; Manojlović D; Radević B; Andjelković Z; Burić B; Savicević M; Nesković G
Srp Arh Celok Lek; 2002 Jul; 130 Suppl 2():43-6. PubMed ID: 12584997
[TBL] [Abstract][Full Text] [Related]
12. Multiple endocrine neoplasia (MEN)--an overview and case report--patient with sporadic bilateral pheochromocytoma, hyperparathyroidism and marfanoid habitus.
Fassbender WJ; Krohn-Grimberghe B; Görtz B; Litzlbauer D; Stracke H; Raue F; Kaiser HE
Anticancer Res; 2000; 20(6C):4877-87. PubMed ID: 11205236
[TBL] [Abstract][Full Text] [Related]
13. [Pheochromocytoma--pathohistologic and immunohistochemical aspects].
Tatić S; Havelka M; Paunović I; Bozić V; Diklic A; Brasanac D; Janković R; Jancić-Zguricas M
Srp Arh Celok Lek; 2002 Jul; 130 Suppl 2():7-13. PubMed ID: 12584991
[TBL] [Abstract][Full Text] [Related]
14. [Does hemangioblastoma exist outside von Hippel-Lindau disease?].
Richard S; Beigelman C; Gerber S; Van Effenterre R; Gaudric A; Sahel M; Binaghi M; De Kersaint-Gilly A; Houtteville JP; Brunon JP
Neurochirurgie; 1994; 40(3):145-54. PubMed ID: 7723921
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Von Hippel-Lindau disease and pheochromocytoma.
Walther MM; Linehan WM
JAMA; 1996 Mar; 275(11):839-40. PubMed ID: 8596219
[No Abstract] [Full Text] [Related]
19. Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A.
Lips CJ; Landsvater RM; Höppener JW; Geerdink RA; Blijham G; van Veen JM; van Gils AP; de Wit MJ; Zewald RA; Berends MJ
N Engl J Med; 1994 Sep; 331(13):828-35. PubMed ID: 7915822
[TBL] [Abstract][Full Text] [Related]
20. Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.
Ritter MM; Frilling A; Crossey PA; Höppner W; Maher ER; Mulligan L; Ponder BA; Engelhardt D
J Clin Endocrinol Metab; 1996 Mar; 81(3):1035-7. PubMed ID: 8772572
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
