These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

103 related articles for article (PubMed ID: 9201016)

  • 1. Familial pheochromocytoma due to mutant von Hippel-Lindau disease gene.
    Mulvihill JJ; Ferrell RE; Carty SE; Tisherman SE; Zbar B
    Arch Intern Med; 1997 Jun; 157(12):1390-1. PubMed ID: 9201016
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. [Familial pheochromocytoma associated with non Hippel-Lindau disease. A family study].
    Unsgård G; Kufaas T; Blika S
    Tidsskr Nor Laegeforen; 1984 Apr; 104(12):786-8. PubMed ID: 6740575
    [No Abstract]   [Full Text] [Related]  

  • 4. [A family with 4 cases of pheochromocytoma and 2 cases of Hippel-Lindau disease].
    Matsubara T; Koyama M; Yoshida S; Itoh T; Horiuchi N; Tateishi R; Wada A; Bito S
    Nihon Rinsho; 1978 Sep; 36(9):3248-53. PubMed ID: 722921
    [No Abstract]   [Full Text] [Related]  

  • 5. Molecular characterization of a pediatric pheochromocytoma with suspected bilateral disease.
    Mircescu H; Wilkin F; Paquette J; Oligny LL; Decaluwe H; Gaboury L; Nolet S; Van Vliet G; Deal C
    J Pediatr; 2001 Feb; 138(2):269-73. PubMed ID: 11174629
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Familial pheochromocytoma associated with a novel mutation in the von Hippel-Lindau gene.
    Gross DJ; Avishai N; Meiner V; Filon D; Zbar B; Abeliovich D
    J Clin Endocrinol Metab; 1996 Jan; 81(1):147-9. PubMed ID: 8550742
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.
    Dannenberg H; van Nederveen FH; Abbou M; Verhofstad AA; Komminoth P; de Krijger RR; Dinjens WN
    J Clin Oncol; 2005 Mar; 23(9):1894-901. PubMed ID: 15774781
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. [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]  

  • 11. Differences in allelic distribution of two polymorphisms in the VHL-associated gene CUL2 in pheochromocytoma patients without somatic CUL2 mutations.
    Duerr EM; Gimm O; Neuberg DS; Kum JB; Clifford SC; Toledo SP; Maher ER; Dahia PL; Eng C
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3207-11. PubMed ID: 10487688
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Paediatric bilateral adrenal phaeochromocytomas in association with a novel mutation in the von Hippel Lindau gene.
    Kim L; Holland AJ; Srinivasan S; Cowell CT; Benn DE; Robinson BG
    J Paediatr Child Health; 2008 Sep; 44(9):514-6. PubMed ID: 18928468
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Inherited pheochromocytoma.
    Neumann HP; Bender BU; Januszewicz A; Janetschek G; Eng C
    Adv Nephrol Necker Hosp; 1997; 27():361-76. PubMed ID: 9408456
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. [How to differentiate sporadic and hereditary pheochromocytoma?].
    Modigliani E
    Ann Pathol; 1999 Dec; 19(6):477-9. PubMed ID: 10617803
    [No Abstract]   [Full Text] [Related]  

  • 16. [Familial pheochromocytoma].
    Tamura N; Nakao K
    Nihon Rinsho; 2006 May; Suppl 1():730-4. PubMed ID: 16776261
    [No Abstract]   [Full Text] [Related]  

  • 17. [Hereditary pheochromocytoma--a family affected by von Hippel-Lindau disease].
    Mertl J; Rovný A; Krepelová A; Prásek J
    Vnitr Lek; 2003 Jul; 49(7):572-5. PubMed ID: 12931443
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Malignant pheochromocytoma combined with multiple renal cell carcinomas and a renal cyst. Indication for von Hippel-Lindau syndrome?].
    Hofmockel G; Manseck A
    Dtsch Med Wochenschr; 2000 Jun; 125(24):767-8. PubMed ID: 10902516
    [No Abstract]   [Full Text] [Related]  

  • 19. von Hippel-Lindau syndrome: a rare syndrome as the clue for the molecular basis of common renal disorders.
    Neumann HP
    Nephrol Dial Transplant; 1995; 10(9):1498-9. PubMed ID: 8559448
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.