Results 81 to 90 of about 4,444,377 (217)
Von Hippel–Lindau Syndrome: A Case Report
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 2009 BACKGROUND AND OBJECTIVE: Von Hippel–lindau syndrome is a rare syndrome. Von Hippel–Lindau is an autosomal dominant condition manifested by cerebellar and spinal hemangioblastomas, retinal angiomas, clear cell RCC, cysts of the pancreas, kidney, and ...
H Shafi, +5 more
doaj
Spontaneous Rupture of a Small Chromophobe Renal Cell Carcinoma Presenting as Wunderlich Syndrome
IJU Case Reports, Volume 9, Issue 6, November 2026.ABSTRACT Introduction Chromophobe renal cell carcinoma rarely causes spontaneous renal hemorrhage and enhances weakly on computed tomography. We report a case in which the tumor was masked by a perirenal hematoma for 11 months. Case Presentation A 46‐year‐old woman presented with spontaneous renal hemorrhage and no visible renal mass.
Naoki Kamimura +7 more
wiley +1 more source
Von Hippel Lindau Disease (Retinal Hemangioblastoma)
, 1992 Von Hippel Lindau Disease with large retinal hemangioblastoma. Continued view of the arteriole and venous channels leading to the tumor. Group with R1_C3a, R1_C3c, R1_C3d. Anatomy: Retina. Pathology: Hemangioblastoma. Disease/Diagnosis: Von Hippel Lindau
William F. Hoyt, MD
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Genetic testing considerations for hereditary duodenopancreatic neuroendocrine tumors
Journal of Neuroendocrinology, Volume 38, Issue 11, November 2026.Abstract The incidence of duodenal and pancreatic neuroendocrine tumors (dpNETs) has increased substantially in recent years. These tumors may be due to syndromic hereditary predisposition syndromes: multiple endocrine neoplasia type 1 (MEN1) or 4 (MEN4), Von Hippel–Lindau disease (VHL), neurofibromatosis type 1 (NF1), or tuberous sclerosis complex ...
Théo Charnay +13 more
wiley +1 more source
Von Hippel Lindau Disease with Photocoagulation Effect
, 1976 Von Hippel Lindau Disease with appearance of Xenon photocoagulation on a mini hemangioblastoma. Anatomy: Retina. Pathology: Hemangioblastoma. Disease/Diagnosis: Von Hippel Lindau disease.
William F. Hoyt, MD
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Journal of Medical Case ReportsBackground While papillary cystadenomas of the epididymis are relatively common, the occurrence of papillary cystadenomas in female individuals, particularly in the ovaries, remains exceedingly rare.
Haifa Bergaoui +10 more
doaj +1 more source
ChemMedChem, Volume 21, Issue 19, 14 October 2026.Can simple linker descriptors guide PROTAC design? Analysis of matched CRBN‐ and VHL‐recruiting degraders shows that basic 2D linker properties may capture trends linked to degradation efficiency, in vitro ADME and physicochemical properties. A practical approach to reduce trial‐and‐error in early targeted protein degradation programs. Targeted protein
Giulia Apprato +3 more
wiley +1 more source
Management of a Case of von Hippel-Lindau for Coronary Artery Bypass Grafting
, 2015 von Hippel-Lindau (VHL) disease is a rare autosomal dominant genetic disorder with retinal and nervous system haemangioblastomas, phaeochromocytoma, renal, pancreatic and endolymphatic tumours.
Geetanjali S. Verma
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