BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 34028413)

  • 21. Von Hippel-Lindau disease type 2 in a Chinese family with a VHL p.W88X truncation.
    Zhang M; Wang J; Jiang J; Zhan X; Ling Y; Lu Z; Guo J; Gao X
    Endocrine; 2015 Feb; 48(1):83-8. PubMed ID: 25069792
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Novel gene mutation in von Hippel-Lindau disease - a report of two cases.
    Wang J; Cao W; Wang Z; Zhu H
    BMC Med Genet; 2019 Dec; 20(1):194. PubMed ID: 31823746
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mosaicism in von Hippel-Lindau disease with severe renal manifestations.
    Wu P; Zhang N; Wang X; Li T; Ning X; Bu D; Gong K
    Clin Genet; 2013 Dec; 84(6):581-4. PubMed ID: 23384228
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Pediatric pheochromocytoma in association with Von Hippel-Lindau disease: Focus on screening strategies.
    Vérot PL; Rabattu PY; Chabre O; Gayot A; Sartelet H; Faguet R; Robert Y; Piolat C
    Arch Pediatr; 2020 Nov; 27(8):497-501. PubMed ID: 33067065
    [TBL] [Abstract][Full Text] [Related]  

  • 25. von Hippel-Lindau Disease: Review of Genetics and Imaging.
    Shanbhogue KP; Hoch M; Fatterpaker G; Chandarana H
    Radiol Clin North Am; 2016 May; 54(3):409-22. PubMed ID: 27153780
    [TBL] [Abstract][Full Text] [Related]  

  • 26. FDG PET/CT detects clinically occult pancreatic cancer in a case of Von Hippel-Lindau syndrome.
    Kulkarni M; Purandare N; Zade A; Agrawal A; Shah S; Rangarajan V
    Clin Nucl Med; 2013 Jul; 38(7):e302-3. PubMed ID: 23486326
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Molecular-genetic diagnostics of von Hippel-Lindau syndrome (VHL) in Bulgaria: first complex mutation event in the VHL gene.
    Glushkova M; Dimova P; Yordanova I; Todorov T; Tourtourikov I; Mitev V; Todorova A
    Int J Neurosci; 2018 Feb; 128(2):117-124. PubMed ID: 28849724
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A Von Hippel-Lindau Disease-Associated Microcystic Adenoma of the Ethmoid Sinus Mimicking Metastatic Clear Cell Renal Cell Carcinoma.
    Tsukamoto S; Koyasu S; Sugimoto A; Matsunaga M; Nakamoto Y
    Clin Nucl Med; 2023 Feb; 48(2):194-196. PubMed ID: 36179325
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Endolymphatic sac tumor with von Hippel-Lindau disease: report of two cases with testing of von Hippel-Lindau gene].
    Su Y; Shen WD; Wang CC; Han WJ; Liu J; Hou ZH; Song ZG; Huang DL; Han DY; Yang SM
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Nov; 48(11):913-8. PubMed ID: 24444636
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Case of parotid mucoepidermoid carcinoma: Expanding the spectrum of von Hippel-Lindau-related neoplasms.
    Berger MH; Kerr DA; Rangel Filho AE; Sargi ZB
    Head Neck; 2017 Mar; 39(3):E51-E54. PubMed ID: 28006088
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Genetic analysis of a family with Von Hippel-Lindau syndrome].
    Lafuente-Sanchis A; Cuevas JM; Alemany P; Cremades A; Zúñiga Á
    Rev Esp Patol; 2017; 50(1):64-67. PubMed ID: 29179968
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Tumors in von Hippel-Lindau Syndrome: From Head to Toe-Comprehensive State-of-the-Art Review.
    Ganeshan D; Menias CO; Pickhardt PJ; Sandrasegaran K; Lubner MG; Ramalingam P; Bhalla S
    Radiographics; 2018; 38(3):849-866. PubMed ID: 29601266
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Prenatal exclusion of von Hippel-Lindau syndrome in a Mexican family carrying a novel VHL gene mutation].
    Chacón-Camacho OF; Benitez-Granados J; Zenteno JC
    Ginecol Obstet Mex; 2013 Apr; 81(4):206-10. PubMed ID: 23720934
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Endolymphatic sac tumors. A source of morbid hearing loss in von Hippel-Lindau disease.
    Manski TJ; Heffner DK; Glenn GM; Patronas NJ; Pikus AT; Katz D; Lebovics R; Sledjeski K; Choyke PL; Zbar B; Linehan WM; Oldfield EH
    JAMA; 1997 May; 277(18):1461-6. PubMed ID: 9145719
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease.
    Hasani-Ranjbar S; Amoli MM; Ebrahim-Habibi A; Haghpanah V; Hejazi M; Soltani A; Larijani B
    Fam Cancer; 2009; 8(4):465-71. PubMed ID: 19649731
    [TBL] [Abstract][Full Text] [Related]  

  • 37. VON HIPPEL-LINDAU DISEASE: Update on Pathogenesis and Systemic Aspects.
    Aronow ME; Wiley HE; Gaudric A; Krivosic V; Gorin MB; Shields CL; Shields JA; Jonasch EW; Singh AD; Chew EY
    Retina; 2019 Dec; 39(12):2243-2253. PubMed ID: 31095066
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A Case of von Hippel-Lindau Disease with Colorectal Adenocarcinoma, Renal Cell Carcinoma and Hemangioblastomas.
    Heo SJ; Lee CK; Hahn KY; Kim G; Hur H; Choi SH; Han KS; Cho A; Jung M
    Cancer Res Treat; 2016 Jan; 48(1):409-14. PubMed ID: 25715769
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Sinonasal renal cell-like adenocarcinoma arising in von Hippel Lindau (VHL) syndrome.
    Maharaj S; Seegobin K; Wakeman K; Chang S; Potts K; Williams B; Redman R
    Oral Oncol; 2022 Feb; 125():105705. PubMed ID: 34998175
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characterization of VHL promoter variants in patients suspected of Von Hippel-Lindau disease.
    Albanyan S; Giles RH; Gimeno EM; Silver J; Murphy J; Faghfoury H; Morel CF; Machado J; Kim RH
    Eur J Med Genet; 2019 Mar; 62(3):177-181. PubMed ID: 30006056
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.