Results 101 to 110 of about 9,097,505 (214)

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
core  

The Von Hippel-Lindau Protein Suppresses Androgen Receptor Activity

, 2014
The androgen receptor (AR) plays a pivotal role in prostate homeostasis and prostate cancer development. To understand the mechanism underlying the regulation of the AR holds a promise for developing novel therapeutic approaches for prostate cancer. Here,
Liu, Xing, Zhang, Wei, Ouyang, Gang, Xiao, WH (reprint author), Chinese Acad Sci, Inst Hydrobiol, Wuhan 430072, Peoples R China., Wang, Jing, Ji, Wei, Xiao, Wuhan   +6 more
core   +1 more source

Medicinal and Crop Protection Chemistry: Breaking Barriers, Building Synergies

ChemMedChem, Volume 21, Issue 16, 27 August 2026.
A unified view of medicinal and crop protection chemistry reveals shared scientific progress, common challenges, and new opportunities for cross‐disciplinary collaboration. Bridging expertise across both fields could accelerate innovation and actively encourage more sustainable solutions.
Giulia Cazzaniga, Giusy L. Fratello, Alexander T. Apostle, Roberto Orru, David M. Barber, Silvia Gazzola   +5 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
core  

Von Hippel Lindau Disease (Retinal Hemangioblastoma)

, 1984
Von Hippel Lindau Disease (Retinal Hemangioblastoma); Small hemangioblastoma on the disc margin at 10:00. Large peripheral hemangioblastoma out of view to the top right seen on R1_C2b. Anatomy: Optic disc. Pathology: Hemangioblastoma.
William F. Hoyt, MD
core  

An Update on the Ophthalmologic Features in the Phakomatoses

Journal of Ophthalmology, 2016
Neurofibromatosis type 1, tuberous sclerosis complex, and Von Hippel-Lindau disease, historically classified as the phakomatoses, are hereditary multisystem disorders characterized by the presence of hamartoma, which carry the risk of malignant ...
Solmaz Abdolrahimzadeh, Andrea Maria Plateroti, Santi Maria Recupero, Alessandro Lambiase   +3 more
doaj   +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
core  

Clinical characteristics and follow‐up of 77 patients with pathogenic fumarate hydratase variants

BJU International, Volume 138, Issue 3, Page 397-399, September 2026.
Matthijs Duijn, Aline M. Tijans, R. Jeroen A. van Moorselaar, Marjoleine F. Broekema, Marleen E. de Lange, Emiel D. Post Uiterweer, Marilyne M. Lange, Naomi Donner, Markus V. Starink, Antoinette Hollestelle, Liselotte P. van Hest, Femke Struik, Patricia J. Zondervan   +12 more
wiley   +1 more source

Von Hippel Lindau Disease (Hemangioblastoma of the Optic Disc)

, 1977
Von Hippel Lindau Disease with a retinal hemangioblastoma on her optic disc. Anatomy: Optic disc. Pathology: Hemangioblastoma. Disease/Diagnosis: Von Hippel Lindau disease. Clinical: No visual symptoms. Patient had cerebellar ataxia.
William F. Hoyt, MD
core  

A Von Hippel–Lindau Syndrome Case Diagnosed While Hospitalized for Major Depression

Von 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.
Furkan Bahadır Alptekin
core   +1 more source