Results 11 to 20 of about 4,444,377 (217)
Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2011 Review on Von Hippel-Lindau, with data on clinics, and the genes ...
Richard, S
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Von Hippel-Lindau Disease [PDF]
Hereditary Cancer in Clinical Practice, 2005 A germline mutation in the Von-Hippel Lindau (VHL) gene predisposes carriers to development of abundantly vascularised tumours in the retina, cerebellum, spine, kidney, adrenal gland and pancreas. Most VHL patients die from the consequences of cerebellar
Hes Frederik J +3 more
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Ожирение и метаболизм, 2011 Von Hippel-Lindau syndrome - a systemic disease manifesting with multiple tumor growth, inherited by autosomal-dominant type with high penetrance. Understanding the pathogenesis of the disease is important for determining the start time of screening for ...
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Indian Journal of Ophthalmology, 1988 Von Hippel Lindan disease is a rare congenital vascular malformation afflicting the retinal and central nervous system blood vessels. A boy aged 12 years suffering from this angiomatosis with bilateral involvement was examined.
Khare M, Varma Rajan
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CNS Lesions in Von Hippel-Lindau Syndrome
Pediatric Neurology Briefs, 1992 Ninety-seven gene carriers of von Hippel-Lindau syndrome (HLS) were studied at the University of Freiburg, Germany, to evaluate the prevalence and location of CNS lesions.
J Gordon Millichap
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Von Hippel-Lindau Disease: Familial Symptom Clusters
Pediatric Neurology Briefs, 1991 The clinical manifestations and prevalence of von Hippel-Lindau syndrome (HLS) were reported from the Department of Medicine, Albert-Ludwigs-Universitat, Freiburg im Breisgau, Germany, and Department of Pathology, University of Zurich, Switzerland.
J Gordon Millichap
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Von Hippel-Lindau Disease and Pheochromocytoma
Pediatric Neurology Briefs, 1993 Nineteen percent of 82 unselected patients with pheochromocytoma studied at the University of Freiburg, Germany, and the University of California, San Diego, were found to be gene carriers of von Hippel-Lindau disease.
J Gordon Millichap
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Suprasellar hemanjioblastomun eşlik ettiği Von Hippel Lindau hastalığı [PDF]
Genel Tıp Dergisi, 2014 von Hippel-Lindau hastalığı; retinal, spinal ve serebellar hemanjioblastom, renal hücreli karsinom, feokromositoma, pankreatik kist ve tümörler, endolenfatik kese tümörleri gibi benign ve malign tümörlerin gelişimi ile karakterize kalıtsal bir ...
Hasan Erdoğan +4 more
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The history of von Hippel-Lindau disease
Journal of Nephrology, 2006 Abstract: von Hippel-Lindau (vHL) disease is a heritable multisystem cancer syndrome that is associated with a germ line mutation of the vHL tumor suppressor gene on the short arm of chromosome 3. Affected individuals are at risk of developing various benign and malignant tumors of the central nervous system, kidneys, adrenal glands ...
MOLINO D. +3 more
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Von Hippel-Lindau Syndrome [PDF]
Hormone Research in Paediatrics, 2015 Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome characterized by the development of multiple vascular tumours. The syndrome is caused by inactivation of the VHL protein (pVHL) and increased production of VEGF, PDGF, and TGF-α. The course of VHL syndrome is associated with the development of multiple vascular tumours.
Iwona Ben-Skowronek, Sylwia Kozaczuk
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