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 *

63 related articles for article (PubMed ID: 13716312)

  • 21. [Bilateral pheochromocytoma. Genetics and treatment].
    Mirallié E; Cariou B; Kraeber-Bodéré F
    Ann Chir; 2005 Apr; 130(4):273-6. PubMed ID: 15847867
    [No Abstract]   [Full Text] [Related]  

  • 22. cDNA microarray analysis assists in diagnosis of malignant intrarenal pheochromocytoma originally masquerading as a renal cell carcinoma.
    Takahashi M; Yang XJ; McWhinney S; Sano N; Eng C; Kagawa S; Teh BT; Kanayama HO
    J Med Genet; 2005 Aug; 42(8):e48. PubMed ID: 16061554
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular pathways linking the pheochromocytoma susceptibility genes.
    Leow MK
    Pediatr Blood Cancer; 2007 Dec; 49(7):1050-1; author reply 1052-3. PubMed ID: 17243134
    [No Abstract]   [Full Text] [Related]  

  • 24. Pheochromocytoma in father and son: report of the eighth known affected kindred.
    GREENBERG RE; GARDNER LI
    J Clin Endocrinol Metab; 1959 Mar; 19(3):351-62. PubMed ID: 13631052
    [No Abstract]   [Full Text] [Related]  

  • 25. Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation.
    Peczkowska M; Cascon A; Prejbisz A; Kubaszek A; Cwikła BJ; Furmanek M; Erlic Z; Eng C; Januszewicz A; Neumann HP
    Nat Clin Pract Endocrinol Metab; 2008 Feb; 4(2):111-5. PubMed ID: 18212813
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A common pathway for genetic events leading to pheochromocytoma.
    Maxwell PH
    Cancer Cell; 2005 Aug; 8(2):91-3. PubMed ID: 16098460
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.
    Astuti D; Hart-Holden N; Latif F; Lalloo F; Black GC; Lim C; Moran A; Grossman AB; Hodgson SV; Freemont A; Ramsden R; Eng C; Evans DG; Maher ER
    Clin Endocrinol (Oxf); 2003 Dec; 59(6):728-33. PubMed ID: 14974914
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. RET expression and neuron-like differentiation of pheochromocytoma and normal chromaffin cells.
    Powers JF; Picard KL; Tischler AS
    Horm Metab Res; 2009 Sep; 41(9):710-4. PubMed ID: 19551609
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation.
    Milos IN; Frank-Raue K; Wohllk N; Maia AL; Pusiol E; Patocs A; Robledo M; Biarnes J; Barontini M; Links TP; de Groot JW; Dvorakova S; Peczkowska M; Rybicki LA; Sullivan M; Raue F; Zosin I; Eng C; Neumann HP
    Endocr Relat Cancer; 2008 Dec; 15(4):1035-41. PubMed ID: 18794325
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Asymptomatic bilateral adrenal pheochromocytoma in a patient with a germline V804M mutation in the RET proto-oncogene.
    Recasens M; Oriola J; Fernández-Real JM; Roig J; Rodríguez-Hermosa JI; Font JA; Galofre P; López-Bermejo A; Ricart W
    Clin Endocrinol (Oxf); 2007 Jul; 67(1):29-33. PubMed ID: 17466010
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Expression of mRNAs for succinate dehydrogenase subunits and related genes in pheochromocytoma.
    Isobe K; Nissato S; Tatsuno I; Yashiro T; Takekoshi K; Kawakami Y
    Ann N Y Acad Sci; 2006 Aug; 1073():253-62. PubMed ID: 17102093
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Genetic testing in pheochromocytoma: increasing importance for clinical decision making.
    Bornstein SR; Gimenez-Roqueplo AP
    Ann N Y Acad Sci; 2006 Aug; 1073():94-103. PubMed ID: 17102076
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Pheochromocytoma-quo vadis?
    Benn DE; Robinson BG
    Nat Clin Pract Endocrinol Metab; 2007 May; 3(5):377. PubMed ID: 17452964
    [No Abstract]   [Full Text] [Related]  

  • 35. Genetics of phaeochromocytoma.
    Maher ER
    Br Med Bull; 2006; 79-80():141-51. PubMed ID: 17339275
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Pheochromocytoma: recent advances and speed bumps in the road to further progress.
    Eisenhofer G
    J Hypertens; 2006 Dec; 24(12):2341-3. PubMed ID: 17082710
    [No Abstract]   [Full Text] [Related]  

  • 37. Genetic basis of phaeochromocytoma and paraganglioma.
    Benn DE; Robinson BG
    Best Pract Res Clin Endocrinol Metab; 2006 Sep; 20(3):435-50. PubMed ID: 16980204
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The effects of urotensin-II on proliferation of pheochromocytoma cells and mRNA expression of urotensin-II and its receptor in pheochromocytoma tissues.
    Zeng ZP; Liu GQ; Li HZ; Fan XR; Liu DM; Tong AL; Zheng X; Liu C
    Ann N Y Acad Sci; 2006 Aug; 1073():284-9. PubMed ID: 17102097
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [The pheochromocytoma of familial character].
    HRADEC E; MARATKA Z; PALECKOVA M
    J Chir (Paris); 1961 Apr; 81():479-86. PubMed ID: 13716312
    [No Abstract]   [Full Text] [Related]  

  • 40. [Familial pheochromocytoma. Discussion of its malignancy and hereditary character: apropos of a case in a child with peculiar secretion].
    Donath A; Käser H; Roos B; Ziegler W; Oetliker O; Colombo JP; Bettex M
    Helv Paediatr Acta; 1965 Apr; 20(1):1-18. PubMed ID: 5828972
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.