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Documents Synchronous and multiple renal cell carcinoma, clear cell and papillary: An approach to clinically.....

IBJU_Ed2_20.indbINTRODUCTION Renal Cell Cancer (RCC) is a heterogeneous disease that is characterized by distinct patholo- gical phenotypes due to the differences in genetic

Documents Angiomatosis retinae

Angiomatosis retinae North Middlesex Hospital, London Von Hippel-Lindau disease or angiomatosis retinae is a rare condition that can present at any age but most commonly

Documents Von Hippel-Lindau Disease

Oxford Regional Genetic Department for patients and families page 2 What is Von Hippel-Lindau disease? Von Hippel-Lindau (VHL) disease is a rare inherited disorder caused

Documents von Hippel-Lindau Disease

von Hippel-Lindau Diseasevon Hippel-Lindau Disease VICKI COUCH, MS; NORALANE M. LINDOR, MD; PAMELA S. KARNES, MD; AND VIRGINIA V. MICHELS, MD An autosomal dominant tumor

Documents Von Hippel-Lindau Syndrome

HRP431323.inddVon Hippel-Lindau Syndrome Introduction Von Hippel-Lindau (VHL) syndrome is a rare autoso- mal dominantly inherited genetic disorder [1] . The dis- ease was

Documents WELIREG is the first and only oral medicine approved to treat adult patients with certain von...

WELIREG is a prescription medicine used to treat adults with von Hippel-Lindau (VHL) disease who need treatment for a type of kidney cancer called renal cell carcinoma (RCC),

Documents Management of von Hippel-Lindau Disease: An Interdisciplinary Review

Review Article Management of von Hippel-Lindau Disease: An Interdisciplinary Review Sabine Schmid a Silke Gillessen b Isabelle Binet c Michael Brändle d Daniel Engeler

Documents Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with...

CASE REPORT von Hippel-Lindau (VHL) disease is an autosomal dominantly inherited disorder, characterized by hemangioblastomas of the retina and central nervous system (CNS);

Documents Von Hippel-Lindau syndrome

Von Hippel-Lindau syndromeVon Hippel-Lindau syndrome Description Von Hippel-Lindau syndrome is an inherited disorder characterized by the formation of tumors and fluid-filled

Documents Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient

TX_1:ABS~AT/TX_2:ABS~ATBoletín Médico del Hospital Infantil de México CLINICAL CASE Abstract Background: Patients with familial erythrocytosis type 2