Results 91 to 100 of about 5,631,965 (202)

Manejo anestésico de feocromocitoma en paciente con enfermedad de Von Hippel-Lindau [PDF]

Revista Chilena de Anestesia, 2022
Nerea Ruiz Andrés, Bonifacio Cimadevilla Calvo, Marina Regato Avilés, José Luis Rábago Moriyón, Pablo Del Olmo Ruiloba   +4 more
doaj   +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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Von Hippel-Lindau syndrome with central nervous system involvement and family history: A case report

Indian Journal of Ophthalmology. Case Reports
Von Hippel-Lindau (VHL) syndrome is a hereditary neoplastic disorder inherited in an autosomal dominant pattern, characterized by the formation of multiple benign and malignant tumors and cysts in various organ systems, including the central nervous ...
Mehul A Shah, Shreya M Shah, Eram Tandel, Nikita Balani, Avani Chudasama   +4 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
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CRISPR/Cas9-mediated editing of VHL in induced pluripotent stem cells: A model for early cell fate in von Hippel-Lindau syndrome

Stem Cell Research
The von Hippel–Lindau (VHL) tumor suppressor gene is crucial for cellular homeostasis, and its loss leads to VHL syndrome. To model early effects of VHL deficiency, we used CRISPR/Cas9 to generate human iPSC lines with heterozygous or homozygous out-of ...
Tim F. Grüner, Haribaskar Ramachandran, Anitha C. Thomas, Barbara Hildebrandt, Sven Gläsker, Jochen Dobner, Andrea Rossi   +6 more
doaj   +1 more source

The history of von Hippel-Lindau disease.

, 2006
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.
ANASTASIO, Pietro, MOLINO D., SEPE J., DE SANTO N. G.   +3 more
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A contemporary overview of multiple endocrine neoplasia syndromes: MEN syndromes 1–5 and beyond

Endocrine Oncology
Multiple endocrine neoplasia (MEN) syndromes constitute a heterogeneous group of hereditary disorders predisposing to endocrine tumours of varying malignant potential.
Raquel A Maggacis, Alexandra Sorvina, Lisa J Hayes, Warrick J Inder, Emily K Brooks, Sunita M C De Sousa   +5 more
doaj   +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
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Terson’s Syndrome in a Patient with von Hippel-Lindau Disease

, 2016
Terson's syndrome is a condition where a preretinal hemorrhage forms as a result of increased intracranial pressure. The elevated intracranial pressure is thought to be transmitted through the veins and the optic nerve sheath to the optic disc and retina,
Luis A. Acaba, Murray, Timothy G, Chenworth, Megan L, Fiona J. Ehlies, Wildner, Andrea C, Aaron S. Gold, Gold, Aaron S, Ehlies, Fiona J, Andrea C. Wildner, Audina M. Berrocal, Acaba, Luis A, Berrocal, Audina M, Timothy G. Murray, Megan L. Chenworth   +13 more
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Composés pour le traitement de la maladie de Von Hippel-Lindau

, 2018
[EN] The invention relates to the use of a selective 2 adrenergic receptor antagonist for treating and preventing a tumor in a patient with von Hippel-Lindau syndrome.
Albiñana, Virginia, Villar Gómez de las Heras, Karina, Botella, Luisa María   +2 more
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