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1970 5
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7,461 results

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Page 1
von Hippel-Lindau disease.
Lonser RR, Glenn GM, Walther M, Chew EY, Libutti SK, Linehan WM, Oldfield EH. Lonser RR, et al. Lancet. 2003 Jun 14;361(9374):2059-67. doi: 10.1016/S0140-6736(03)13643-4. Lancet. 2003. PMID: 12814730 Review.
von Hippel-Lindau disease is a heritable multisystem cancer syndrome that is associated with a germline mutation of the VHL tumour suppressor gene on the short arm of chromosome 3. ...We present an overview of the clinical aspects, management, and treatment o …
von Hippel-Lindau disease is a heritable multisystem cancer syndrome that is associated with a germline mutation of the …
Von Hippel-Lindau Syndrome.
Ben-Skowronek I, Kozaczuk S. Ben-Skowronek I, et al. Horm Res Paediatr. 2015;84(3):145-52. doi: 10.1159/000431323. Epub 2015 Aug 5. Horm Res Paediatr. 2015. PMID: 26279462 Free article. Review.
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome characterized by the development of multiple vascular tumours. ...
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome characterized by the development of multiple vascular t …
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. Aronow ME, et al. Retina. 2019 Dec;39(12):2243-2253. doi: 10.1097/IAE.0000000000002555. Retina. 2019. PMID: 31095066 Review.
METHODS: A PubMed search of the English language literature was reviewed using the following search terms: von Hippel-Lindau, von Hippel-Lindau disease, and VHL. Of 6,696 publications, the most current and pertinent information related to …
METHODS: A PubMed search of the English language literature was reviewed using the following search terms: von Hippel-Linda …
von Hippel-Lindau syndrome.
Chou A, Toon C, Pickett J, Gill AJ. Chou A, et al. Front Horm Res. 2013;41:30-49. doi: 10.1159/000345668. Epub 2013 Mar 19. Front Horm Res. 2013. PMID: 23652669 Review.
von Hippel-Lindau (VHL) disease is an autosomal-dominant familial cancer syndrome associated with mutations of the VHL tumor suppressor gene (3p25-26). ...
von Hippel-Lindau (VHL) disease is an autosomal-dominant familial cancer syndrome associated with mutations of the VHL …
Von Hippel-Lindau disease-associated renal cell carcinoma: a call to action.
Larcher A, Rowe I, Belladelli F, Fallara G, Raggi D, Necchi A, Montorsi F, Capitanio U, Salonia A; OSR VHL Program. Larcher A, et al. Curr Opin Urol. 2022 Jan 1;32(1):31-39. doi: 10.1097/MOU.0000000000000950. Curr Opin Urol. 2022. PMID: 34783716 Review.
PURPOSE OF REVIEW: While the molecular and genetic bases of Von Hippel-Lindau (VHL) disease have been extensively investigated, limited evidence is available to guide diagnosis, local or systemic therapy, and follow-up. ...
PURPOSE OF REVIEW: While the molecular and genetic bases of Von Hippel-Lindau (VHL) disease have been extensively inves …
Von Hippel-Lindau disease.
Kaelin WG. Kaelin WG. Annu Rev Pathol. 2007;2:145-73. doi: 10.1146/annurev.pathol.2.010506.092049. Annu Rev Pathol. 2007. PMID: 18039096 Review.
von Hippel-Lindau disease, which is characterized by an increased risk of hemangioblastomas, clear cell renal carcinomas, and pheochromocytomas, is caused by inactivating mutations of the VHL tumor suppressor gene. ...
von Hippel-Lindau disease, which is characterized by an increased risk of hemangioblastomas, clear cell renal carcinoma …
Von Hippel-Lindau syndrome.
Neumann HP, Lips CJ, Hsia YE, Zbar B. Neumann HP, et al. Brain Pathol. 1995 Apr;5(2):181-93. doi: 10.1111/j.1750-3639.1995.tb00592.x. Brain Pathol. 1995. PMID: 7670659 Review.
After a decade of intensive clinical and molecular genetic efforts the von Hippel-Lindau (VHL) gene was cloned in 1993. The open reading frame encodes the putative protein of 284 amino acids. ...
After a decade of intensive clinical and molecular genetic efforts the von Hippel-Lindau (VHL) gene was cloned in 1993. …
von Hippel-Lindau disease.
Connor JM. Connor JM. Q J Med. 1990 Nov;77(283):1099-100. doi: 10.1093/qjmed/77.2.1099. Q J Med. 1990. PMID: 2274655 No abstract available.
[Von Hippel-Lindau syndrome].
Reith W, Körner H. Reith W, et al. Radiologe. 2013 Dec;53(12):1104-6. doi: 10.1007/s00117-013-2606-2. Radiologe. 2013. PMID: 24292403 Review. German.
Von Hippel-Lindau syndrome is an autosomal dominant inherited phacomatosis with a predisposition for the central nervous system and retina. ...Magnetic resonance imaging (MRI) of the neuroaxis is indicated in all patients with a suspicion of von Hip …
Von Hippel-Lindau syndrome is an autosomal dominant inherited phacomatosis with a predisposition for the central nervou …
von Hippel-Lindau disease-related neoplasia with an emphasis on renal manifestations.
Tekin B, Erickson LA, Gupta S. Tekin B, et al. Semin Diagn Pathol. 2024 Jan;41(1):20-27. doi: 10.1053/j.semdp.2023.11.003. Epub 2023 Nov 8. Semin Diagn Pathol. 2024. PMID: 37980175 Review.
von Hippel-Lindau (VHL) disease is characterized by biallelic inactivation of the VHL gene leading to abnormal or absent VHL protein function, and constitutive activation of hypoxia-inducible factors (HIF) that leads to pro-tumorigenic signaling. ...
von Hippel-Lindau (VHL) disease is characterized by biallelic inactivation of the VHL gene leading to abnormal or absen …
7,461 results