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675 related items for PubMed ID: 25715769
1. 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 [Abstract] [Full Text] [Related]
2. von Hippel Lindau disease with colon adenocarcinoma, renal cell carcinoma and adrenal pheochromocytoma. Zinnamosca L, Laudisi A, Petramala L, Marinelli C, Roselli M, Vitolo D, Montesani C, Letizia C. Intern Med; 2013 Jan; 52(14):1599-603. PubMed ID: 23857093 [Abstract] [Full Text] [Related]
3. A case of von Hippel-Lindau disease with bilateral pheochromocytoma, renal cell carcinoma, pelvic tumor, spinal hemangioblastoma and primary hyperparathyroidism. Arao T, Okada Y, Tanikawa T, Inatomi H, Shuin T, Fujihira T, Yamashita H, Tanaka Y. Endocr J; 2002 Apr; 49(2):181-8. PubMed ID: 12081237 [Abstract] [Full Text] [Related]
4. [Analysis of spinal cord hemangioblastoma in von Hippel-Lindau disease]. Nakashima H, Tokunaga K, Tamiya T, Matsumoto K, Ohmoto T, Furuta T. No Shinkei Geka; 1999 Jun; 27(6):533-40. PubMed ID: 10396736 [Abstract] [Full Text] [Related]
5. [Von Hippel-Lindau disease: recent genetic progress and patient management. Francophone Study Group of von Hippel-Lindau Disease (GEFVH)]. Richard S, Giraud S, Beroud C, Caron J, Penfornis F, Baudin E, Niccoli-Sire P, Murat A, Schlumberger M, Plouin PF, Conte-Devolx B. Ann Endocrinol (Paris); 1998 Jun; 59(6):452-8. PubMed ID: 10189987 [Abstract] [Full Text] [Related]
6. [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 Jun; 50(1):64-67. PubMed ID: 29179968 [Abstract] [Full Text] [Related]
7. Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau disease. Faiyaz-Ul-Haque M, Jamil M, Aslam M, Abalkhail H, Al-Dayel F, Basit S, Nawaz Z, Zaidi SHE. Cancer Genet; 2020 May; 243():1-6. PubMed ID: 32179488 [Abstract] [Full Text] [Related]
8. Genotype-phenotype correlations in VHL exon deletions. McNeill A, Rattenberry E, Barber R, Killick P, MacDonald F, Maher ER. Am J Med Genet A; 2009 Oct; 149A(10):2147-51. PubMed ID: 19764026 [Abstract] [Full Text] [Related]
9. Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing. Liu F, Calhoun B, Alam MS, Sun M, Wang X, Zhang C, Haldar K, Lu X. BMC Med Genet; 2020 Feb 27; 21(1):42. PubMed ID: 32106822 [Abstract] [Full Text] [Related]
10. 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 27; 39(3):E51-E54. PubMed ID: 28006088 [Abstract] [Full Text] [Related]
11. von Hippel-Lindau syndrome. Chou A, Toon C, Pickett J, Gill AJ. Front Horm Res; 2013 Mar 27; 41():30-49. PubMed ID: 23652669 [Abstract] [Full Text] [Related]
12. Genotype-phenotype analysis of von Hippel-Lindau syndrome in Korean families: HIF-α binding site missense mutations elevate age-specific risk for CNS hemangioblastoma. Lee JS, Lee JH, Lee KE, Kim JH, Hong JM, Ra EK, Seo SH, Lee SJ, Kim MJ, Park SS, Seong MW. BMC Med Genet; 2016 Jul 20; 17(1):48. PubMed ID: 27439424 [Abstract] [Full Text] [Related]
13. Extraneuraxial hemangioblastoma: A clinicopathologic study of 10 cases with molecular analysis of the VHL gene. Muscarella LA, Bisceglia M, Galliani CA, Zidar N, Ben-Dor DJ, Pasquinelli G, la Torre A, Sparaneo A, Fanburg-Smith JC, Lamovec J, Michal M, Bacchi CE. Pathol Res Pract; 2018 Aug 20; 214(8):1156-1165. PubMed ID: 29941223 [Abstract] [Full Text] [Related]
14. Von Hippel-Lindau syndrome. A pleomorphic condition. Friedrich CA. Cancer; 1999 Dec 01; 86(11 Suppl):2478-82. PubMed ID: 10630173 [Abstract] [Full Text] [Related]
15. von Hippel-Lindau gene deletion detected in the stromal cell component of a cerebellar hemangioblastoma associated with von Hippel-Lindau disease. Vortmeyer AO, Gnarra JR, Emmert-Buck MR, Katz D, Linehan WM, Oldfield EH, Zhuang Z. Hum Pathol; 1997 May 01; 28(5):540-3. PubMed ID: 9158701 [Abstract] [Full Text] [Related]
16. Clinical and molecular characterization of Brazilian families with von Hippel-Lindau disease: a need for delineating genotype-phenotype correlation. Gomy I, Molfetta GA, de Andrade Barreto E, Ferreira CA, Zanette DL, Casali-da-Rocha JC, Silva WA. Fam Cancer; 2010 Dec 01; 9(4):635-42. PubMed ID: 20567917 [Abstract] [Full Text] [Related]
17. [A case of renal cell carcinoma associated with von Hippel-Lindau disease and the necessity for family genetic diagnosis]. Nanri M, Uda M, Iguchi Y, Gouya N, Toma H, Kihara T. Hinyokika Kiyo; 1999 Nov 01; 45(11):755-8. PubMed ID: 10637737 [Abstract] [Full Text] [Related]
18. Pheochromocytoma and clear-cell renal carcinoma in a child with von Hippel-Lindau disease: a patient report. Ferragut J, Caimari M, Rituerto B, Gómez-Rivas B, Herrera M, Alonso F. J Pediatr Endocrinol Metab; 1999 Nov 01; 12(4):579-82. PubMed ID: 10417977 [Abstract] [Full Text] [Related]
19. [A family of von Hippel-Lindau disease with renal cell carcinoma--case report and review of the literature]. Ito F, Uda M, Toma H. Hinyokika Kiyo; 1991 Feb 01; 37(2):157-62. PubMed ID: 2048495 [Abstract] [Full Text] [Related]
20. Hemangioblastoma of the Peripheral Nervous System: A Critical Analysis of Its Rarity in Von Hippel-Lindau Disease. Murthy NK, Lonser RR, Spinner RJ. World Neurosurg; 2021 Oct 01; 154():e707-e709. PubMed ID: 34343683 [Abstract] [Full Text] [Related] Page: [Next] [New Search]