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  1. 181
    “…CASE PRESENTATION: A 21-year-old woman suffered from decreased vision in the right eye and was diagnosed with retinal capillary hemangioblastomas associated with Von Hippel–Lindau syndrome. The patient underwent two 23-G pars plana vitrectomies (PPVs), soon after which typical signs of SO manifested. …”
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    Case report: Sympathetic ophthalmia after vitrectomies in a patient with Von Hippel–Lindau syndrome
  2. 182
    “…They account for 2 % of all intracranial neoplasms, 7 %–12 % of posterior fossa tumours. 60–75 % cases of hemangioblastomas occur sporadically and rest 25 % to 40 % occur in genetically inherited in the autosomal dominant neoplasia syndrome known as Von Hippel-Lindau (VHL) disease with mutation occurring on chromosome 3p. …”
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    Von-Hippel Lindau (VHL) syndrome with bilateral cerebellar hemangioblastomas and retinal angiomas: A rare presentation
  3. 183
    “…Von Hippel–Lindau (VHL) disease is an autosomal-dominant syndrome caused by mutations in the VHL gene, located on the short arm of chromosome 3. …”
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    Von Hippel Lindau Disease with central nervous system and multiple visceral manifestations: A case report
  4. 184
    “…Genomic DNA analysis showed no mutation in the von Hippel-Lindau (VHL) genes. A surgical specimen obtained from a lesion in the cauda equina showed pathological findings identical to those of the cerebellar HB that had been resected 10 yr earlier. …”
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    Disseminated Hemangioblastomatosis of the Central Nervous System without von Hippel-Lindau Disease: A Case Report
  5. 185
    “…Retinal hemangioblastomas are the most common manifestation of Von Hippel-Lindau (VHL) disease [1-3]. While peripheral retinal hemangioblastomas may be treated by thermal laser treatment or cryotherapy, optic nerve and macular lesions are more difficult to treat [4, 5]. …”
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    Long-Term Use of Intravitreal Bevacizumab (Avastin) for the Treatment of Von Hippel-Lindau Associated Retinal Hemangioblastomas
  6. 186
    “…Von Hippel–Lindau disease (VHL) comprises a series of complicated clinical manifestations. …”
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    A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature
  7. 187
    “…Von Hippel-Lindau (VHL) disease results from the inactivation of the VHL gene and is characterized by highly vascular tumors. …”
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    EAF2 loss enhances angiogenic effects of Von Hippel-Lindau heterozygosity on the murine liver and prostate
  8. 188
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    Regulation of tyrosine-hydroxylase (TH) gene expression by hypoxia and von Hippel-Lindau tumor suppressor complex
  9. 189
    “…Herein, we describe the clinical characteristics and the management strategy of a patient with von Hippel-Lindau (VHL) disease who had multiple, bilateral pheochromocytomas as well as bilateral renal masses, pancreatic masses, and a paracaval mass. …”
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    Adrenal Cortex-Sparing Surgery for Bilateral Multiple Pheochromocytomas in a Patient with Von Hippel-Lindau Disease
  10. 190
    “…Von Hippel-Lindau disease (VHL disease) is a hereditary cancer predisposition syndrome caused by mutations of the von Hippel-Lindau tumor suppressor gene. …”
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    Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease
  11. 191
    por Kaloostian, PE, Taylor, CL
    Publicado 2012
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    Supratentorial dural-based haemangioblastoma in a Native American patient without Von Hippel Lindau Syndrome
  12. 192
    “…Von Hippel-Lindau (VHL) syndrome is a rare neoplastic disorder characterized by central nervous system (CNS) and visceral tumors. …”
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    Von Hippel-Lindau Syndrome: Demonstration of Entire Disease Spectrum with (68)Ga-DOTANOC PET-CT
  13. 193
    “…von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited neoplastic syndrome that may lead to pancreatic masses and obstructive jaundice. …”
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    Obstructive jaundice due to von Hippel-Lindau disease-associated pancreatic lesions: A case report
  14. 194
    “…INTRODUCTION: Retinal hemangioblastoma is one of the most common tumors in von Hippel-Lindau disease. In addition to the classical pathological characteristics of von Hippel-Lindau disease, we report, for what we believe to be the first time, a severe and rare ocular complication characterized by neovascularization in the cornea and iris. …”
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    Pathology characteristics of ocular von Hippel-Lindau disease with neovascularization of the iris and cornea: a case report
  15. 195
    “…OBJECTIVE: Von Hippel-Lindau (VHL) disease is a rare autosomal dominant cancer syndrome. …”
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    AB181. Telomere shortening is associated with genetic anticipation in Chinese Von Hippel-Lindau disease families
  16. 196
    “…Very scarce literature is available regarding supratentorial HBL without von Hippel–Lindau (VHL) syndrome in an adult. We reviewed the literature and PubMed advanced search showed only a few results of supratentorial HBL without VHL syndrome. …”
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    Supratentorial haemangioblastoma without von Hippel–Lindau syndrome in an adult: A rare tumor with review of literature
  17. 197
    “…BACKGROUND: Von Hippel-Lindau (VHL) disease is a hereditary tumor disorder caused by mutations or deletions of the VHL gene. …”
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    Clinical and Genetic Investigation of a Multi-generational Chinese Family Afflicted with Von Hippel-Lindau Disease
  18. 198
    “…Patients affected with von Hippel–Lindau disease are at risk of developing multiple independent clear cell renal carcinomas. …”
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    Patient-specific factors influence somatic variation patterns in von Hippel–Lindau disease renal tumours
  19. 199
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    The von Hippel-Lindau Chuvash mutation in mice alters cardiac substrate and high-energy phosphate metabolism
  20. 200
    “…Hypoxia-inducible factor (HIF)-1α and HIF-2α play an important role in liver fibrosis. von Hippel–Lindau protein (VHL), a key mediator of HIF-α, regulates fibrosis in an organ- and cell-specific way. …”
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    Reduction of hepatic fibrosis by overexpression of von Hippel–Lindau protein in experimental models of chronic liver disease
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