Results 101 to 110 of about 4,444,377 (217)
Von Hippel Lindau Disease (Retinal Hemangioblastoma)
Von Hippel Lindau Disease (Retinal Hemangioblastoma); Small hemangioblastoma on the disc margin at 10:00. Large peripheral hemangioblastoma out of view to the top right seen on R1_C2b. Anatomy: Optic disc. Pathology: Hemangioblastoma.
William F. Hoyt, MD
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Von Hippel- Lindau syndrome (case report)
Von Hippel-Lindau (VHL) sendromu nadir görülen heredofamilyal bir hastalıktır. Klasik bulgulan retinatla anjiomlar ve serebellumda hemanjioblastomlardır.
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Partial deletion of 3p in Von Hippel-Lindau renal cell carcinoma
Genetik, deletion, kromosom 3, von Hippel-Lindau ...
Nørby, Søren +3 more
core +1 more source
Elias Chelala, Ali Dirani, Ali Fadlallah Saint-Joseph University, Faculty of Medicine, Beirut, Lebanon Abstract: We report a case of a patient known to have a von Hippel–Lindau disease with documented progressive juxtapapillary retinal capillary ...
Chelala E, Dirani A, Fadlallah A
doaj
MR Imaging Findings of Supratentorial Meningeal Hemangioblastoma: A Case Report
Hemangioblastomas account for 1.1–2.5% of intracranial neoplasms. These tumors most commonly occur in the cerebellum. A 77-year-old woman had a hemangioblastoma, which showed the supratentorial meningeal mass without any history of von Hippel-Lindau ...
Gi Hong Kim +3 more
doaj +1 more source
Von Hippel Lindau Disease Associated with Increased ICP
Von Hippel Lindau Disease; Optic disc lesion with hemorrhage from it in a patient with acute intracranial pressure elevation from a posterior fossa hemangioblastoma. Anatomy: Optic disc. Pathology: Hemangioblastoma.
William F. Hoyt, MD
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Il caprtolo descrive dli aspetti clinici della sindrome di Von Hippel-Lindau (VHL) è una malattia a carattere ereditario, a trasmissione autosomica dominante con elevata penetranza, caratterizzata dall’associazione di varie ...
BONDANELLI, Marta
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A Von Hippel–Lindau Syndrome Case Diagnosed While Hospitalized for Major Depression
Von Hippel–Lindau syndrome (VHL) is a rare genetic disorder inherited in an autosomal dominant manner. It progresses with the presence of cranial and visceral organ tumors.
Furkan Bahadır Alptekin
core +1 more source
Supplementary Data from Improved Identification of von Hippel-Lindau Gene Alterations in Clear Cell Renal ...
Hellena Kollarova (197814) +28 more
core +1 more source
Compounds for treating Von Hippel-Lindau disease
[EN] The invention relates to the use of a selective 2 adrenergic receptor antagonist for treating and preventing a tumor in a patient with von Hippel-Lindau syndrome.
Albiñana, Virginia +2 more
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