Results 21 to 30 of about 4,444,377 (217)
Von Hippel-Lindau's Disease [PDF]
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 1976 SUMMARY:A patient with Von Hippel-Lindau's disease was followed from the time of diagnosis to the time of his death 13 years later. He was asymptomatic when the diagnosis was made, although a hemangioblastoma of the medulla was found on angiography. The patient's course and autopsy are described and the features of this disease are reviewed.
R G, Miller +3 more
openaire +2 more sources
Laparoscopic partial adrenalectomy for bilateral pheochromocytomas in a boy with von Hippel-Lindau disease [PDF]
, 2000 Objectives: In adults, increasing numbers of adrenalectomies for pheochromocytomas are performed laparoscopically. We report for the first time laparoscopic bilateral subtotal adrenalectomy for pheochromocytomas in an 8-year-old boy with von Hippel ...
Elsner, Romy +5 more
core +1 more source
Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease. [PDF]
, 1996 Inherited pheochromocytomas are often part of familial syndromes, especially multiple endocrine neoplasia type 2 (MEN 2), retinal cerebellar hemangioblastomatosis [von Hippel-Lindau (vHL) disease] or neurofibromatosis type 1.
Crossey, P.A. +7 more
core +1 more source
Structure-guided design and optimization of small molecules targeting the protein-protein interaction between the von hippel-lindau (VHL) E3 ubiquitin ligase and the hypoxia inducible factor (HIF) alpha subunit with in vitro nanomolar affinities [PDF]
, 2014 E3 ubiquitin ligases are attractive targets in the ubiquitin-proteasome system, however, the development of small-molecule ligands has been rewarded with limited success.
Dias, David M +20 more
core +1 more source
Von Hippel–Lindau disease [PDF]
, 2015 von Hippel-Lindau (VHL) disease is an inheritable condition with an incidence of 1 in 36000 live births. Individuals with VHL develop benign and malignant tumors including retinal and central nervous system hemangioblastomas, clear cell renal cell carcinomas (RCC), pheochromocytomas, pancreatic neuroendocrine tumors and endolymphatic sac tumors (ELSTs).
Prashant, Chittiboina, Russell R, Lonser
openaire +2 more sources
[Von Hippel-Lindau disease]. [PDF]
Nederlands tijdschrift voor geneeskunde, 2000 Von Hippel-Lindau disease (VHL) is an autosomal dominant inherited cancer syndrome. The disease was diagnosed in three patients: a 22-year-old woman who presented with decreased vision due to retinal angiomatosis and in whom a renal carcinoma was diagnosed five years later at a routine VHL analysis, a man aged 44 who died with bilateral renal cysts and
Los, M. +3 more
openaire +5 more sources
대한영상의학회지, 2015 Hemangioblastoma is a benign vascular neoplasm of the central nervous system that occurs frequently in the cerebellum and other areas of the central nervous system including spinal cord and brainstem.
Ok Hwa Kim
doaj +1 more source
Oncology Reviews, 2011 Von Hippel-Lindau disease is a rare autosomal dominant inherited disorder that predisposes the occurrence of cysts and various types of cancers such as hemangioblastoma, pheochromocytoma, renal cell carcinoma and more rarely pancreatic tumors.
Giuseppe Lombardi +5 more
doaj +1 more source
Submacular sclerosing capillary hemangioblastoma
American Journal of Ophthalmology Case Reports, 2018 Purpose: To report a case of submacular cystic lesion that turned out to be a sclerosing capillary hemangioblastoma. The retinal capillary hemangioblastoma may arise as a part of von Hippel-Lindau syndrome 1 however, they may occur as an isolated entity ...
Hany S. Hamza, Abdelrahman M. Elhusseiny
doaj +1 more source
Офтальмохирургия, 2018 Actuality. Von Hippel-Lindau disease is a rare autosomal dominant multi-systemic disease, characterized by the presence of vascular formations (angiomas) of different localization.
E. V. Boyko +3 more
doaj +1 more source