Results 111 to 120 of about 9,097,505 (214)

Von Hippel Lindau Disease Pathology of Mini Hemangioblastoma

open access: yes, 1976
Von Hippel Lindau Disease. Pathologic appearance of flat preparation of retina from necropsy study. Trypsin digestion study of retinal vascular bed with a mini VHL lesion. Anatomy: Retina. Pathology: Hemangioblastoma. Disease/Diagnosis: Von Hippel Lindau
William F. Hoyt, MD
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A histopathological connection between a fatal endolymphatic sac tumour and von Hippel–Lindau disease from 1960

open access: yes, 2017
Objective:To highlight a case from 1960 connecting endolymphatic sac tumour and von Hippel–Lindau disease.Case report:In 1960, a 24-year-old woman presented with unilateral hearing loss, pulsatile tinnitus and a mass visible on otoscopy.
J A Bellairs, M B Gluth
core   +1 more source

Von Hippel Lindau Disease Associated with Increased ICP

open access: yes, 1973
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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Evaluation of the safety and effectiveness of oral propranolol in patients with von Hippel-Lindau disease and retinal hemangioblastomas: phase III clinical trial

open access: yes, 2019
6 p.-3 fig.-1 tab.Background von Hippel-Lindau disease (VHL) is a multisystem cancer syndrome caused by mutations in the VHL gene. Retinal hemangioblastoma is one of the most common tumours, and when it appears near the optic nerve, its treatment is ...
Villar Gómez de las Heras, Karina   +11 more
core   +1 more source

Von Hippel- Lindau syndrome (case report)

open access: yes, 1990
Von Hippel-Lindau (VHL) sendromu nadir görülen heredofamilyal bir hastalıktır. Klasik bulgulan retinatla anjiomlar ve serebellumda hemanjioblastomlardır.

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Masive enterorrhagia in patients suffering from hippel-lindau disease

open access: yesActa Médica del Centro, 2008
The Von Hippel Lindau disease is an autosomic-dominant neoplasia syndrome produced by a delection or mutation of tumor suppressor gene of chromosome 3p25. It was descripted by the German pathologist Arvid Lindau and the ophthalmologist Eugene Von Hippel,
Jorge Luis González Jara   +2 more
doaj  

Huge pancreas helps diagnosis in von Hippel-Lindau disease.

open access: yes, 2006
We describe five patients diagnosed with von Hippel-Lindau disease who complained of abdominal distension, pain and discomfort for a long time. All patients underwent ultrasonography, CT scan and MRI, which showed huge pancreas filled with multiple cysts.
KARATAĞ, OZAN   +4 more
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ENFERMEDAD DE VON HIPPEL-LINDAU Y EMBARAZO

open access: yesRevista Chilena de Obstetricia y Ginecología, 2005
La Enfermedad de Von Hippel-Lindau es un síndrome hereditario, autosómico dominante asociado a la mutación de un gen supresor tumoral localizado en cromosoma 3p25-26 que tiene riesgo genético esperado de desarrollar hemangioblastoma múltiple en cerebro ...
Jorge Hasbun H.   +2 more
doaj  

Compounds for treating Von Hippel-Lindau disease

open access: yes, 2018
[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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Tumor neuroendocrino del páncreas en paciente con enfermedad de Von Hippel Lindau Neuroendocrine pancreatic tumor in a patient with Von Hippel Lindau disease

open access: yesRevista Cubana de Medicina, 2008
Se presentó el caso de una paciente de 30 años de edad con antecedentes familiares de enfermedad de Von Hippel Lindau (VHL), intervenida quirúrgicamente 8 años antes por hemangioblastoma del cerebelo, que en pesquisa periódica con ecografía para ...
Luis Senra Armas   +5 more
doaj  

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