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Orvosi cikkek
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Intrafamilial Variability of Ocular Manifestations of von Hippel-Lindau Disease. Author links open overlay panelRandy ChristopherBowenMD, MS1H. CulverBoldtMD12Robert F.MullinsPhD12Matthew G.FieldMD, PhD1Louisa M.AffatigatoBS12Jeremy M.HoffmannBS12James C.FolkMD1Karen M.GehrsMD1Ian C.HanMD12Elliott H.SohnMD12Stephen R.RussellMD12Edwin M.StoneMD, PhD12Budd A.TuckerPhD12Elaine M.BinkleyMD12
Ophthalmology Retina Volume 6, Issue 1, January 2022, Pages 89-91
- FDA Approves Belzutifan for Cancers Associated With von Hippel-Lindau Disease
- Anne-Marie Vanbinst et al.: A focused 35-minute whole body MRI screening protocol for patients with von Hippel-Lindau disease
- Marie T. Krüger, Christine Steiert, Sven Gläsker and Jan-Helge Klingler MD 1
Minimally invasive resection of spinal hemangioblastoma: feasibility and clinical results in a series of 18 patients. Journal of Neurosurgery
- Surya P.Redman et al: Von Hippel-Lindau and Hereditary Pheochromocytoma/Paraganglioma Syndromes: Clinical Features, Genetics, and Surveillance Recommendatios in Childhood
- Miguel-Angel Díaz-Castellanos, Karina Villar Gómez de las Heras, Tamara Díaz-Redondo, Encarnación González-Flores, Virginia Albinana, Luisa-María Botella: Case Report: Propranolol increases the therapeutic response to temozolomide in a patient with metastatic paraganglioma [version 1; referees: awaiting peer review]
- EMA’s final opinion: Gadolinium-containing contrast agents
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Marie Louise Molgaard Binderup MD, PhD: von Hippel-Lindau szindróma (VHL): a kontroll vizsgálatok jelentősége (webinar 2018)
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Marie Louise Molgaard Binderup MD, PhD: von Hippel-Lindau disease (vHL): the importance of screening (webinar 2018)
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Beatriz González-Rodríguez*, Virginia Albinana, AM Cuesta, Karina Villar-Gómez de las Heras, Luisa María Botella, Rosa María Jiménez-Escribano:Repurposing propranolol for the treatment of von Hippel-Lindau syndrome
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Hartmut P. H. Neumann: Von Hippel-Lindau-szindróma.
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Russell R Lonser et al.: Von Hippel-Lindau disease.
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Gergics Péter et al.: A nagy géndeletiók kimutatásának
módszerei és alkalmazásuk egyes örökletes betegségekben.
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Gergics Péter et al.: Germline VHL gene mutations in Hungarian families with von
Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomas.
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Attila Patócs et al.: Ser80Ile mutation and a concurrent Pro25Leu variant of the VHL
gene in an extended Hungarian von Hippel-Lindau family.
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VHL-Europa alapító tagja
www.vhl-europa.org
