Results 11 to 20 of about 5,631,965 (202)
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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Idiopathic interstitial pneumonia in a patient with von Hippel-Lindau syndrome: a first case. [PDF]
ERJ Open Res, 2023 Although the mechanisms are not known, this is a case of progressive interstitial lung involvement, with a NSIP radiological pattern, evolving in pulmonary fibrosis in a patient with von Hippel-Lindau syndrome, without extrapulmonary fibrosis.
Morlacchi LC +5 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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罕见病研究, 2023 Von Hippel-Lindau (VHL) syndrome, also known as cerebral retinal angiomatosis, is a kind of neuroendocrine tumor. The incidence rate is high, and the heredity is very high, which can involve the retina, central nervous system, various organs and various ...
PU Peng +3 more
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New Prospects on Neuroimaging in Von Hippel Lindau Disease—A Narrative Review
Diagnostics(1) Background: Hemangiomas in Von Hippel-Lindau (VHL) syndrome patients are typically benign but pose threats due to their vital locations involving the central nervous system and the retina.
Nikodem Pietrzak +3 more
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A Von Hippel-Lindau Syndrome Case Diagnosed While Hospitalized for Major Depression. [PDF]
Psychiatry Clin PsychopharmacolVon 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.
Alptekin FB.
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VON HIPPEL-LINDAU SYNDROME: ASPECTS OF TREATMENT AND MANAGEMENT. CASE REPORT AND LITERATURE REVIEW [PDF]
Архивъ внутренней медицины, 2019 The steadily growing interest in studying of endocrine genetics is driven not only by the search for new pathologies but also by the most pressing need to develop methods for early diagnosis, treatment and management of patients.
I. I. Larina +10 more
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Bilateral pheochromocytoma as first manifestation of von Hippel-Lindau disease: a case report [PDF]
The Turkish Journal of Pediatrics, 2012 Von Hippel-Lindau syndrome is an autosomal dominant disorder that includes susceptibility to hemangioblastomas of the eyes and central nervous system, renal clear cell carcinoma, multiple pancreatic cysts, serous cystadenomas and pancreatic ...
Gönül Catli +5 more
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A Family case of von Hippel-Lindau syndrome [PDF]
Problems of EndocrinologyVon Hippel-Lindau syndrome (FHL) is a rare autosomal dominant disease that leads to the formation of multiple organ tumor syndrome. The pathology is primarily caused by the inactivation of the VHL gene, which is located on chromosome 3 (3p25/26) and encodes ubiquitin ligase, which destroys hypoxia-induced factor-1α (HIF-1α). The genetic defect leads to
R. A. Atanesyan +5 more
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