Results 101 to 110 of about 9,530,886 (208)

Epidural anaesthesia for Caesarean section in a patient with von Hippel-Lindau disease

, 2001
Von Hippel-Lindau disease is a rare autosomal dominant disease with incomplete penetrance and variable expression and is characterized by diffuse haemangioblastomas of the central nervous system and viscera.
Demiraran, Y, Utku, Tuğhan, Ozgon, Mustafa, Bozkurt, P, Bozkurt, Pınar   +4 more
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Von Hippel Lindau Disease [PDF]

The Journal of Pediatrics, 2019
Deniz, Hos, Claus, Cursiefen, Claudia, Dahlke   +2 more
openaire   +3 more sources

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

Von Hippel- Lindau syndrome (case report)

, 1990
Von Hippel-Lindau (VHL) sendromu nadir görülen heredofamilyal bir hastalıktır. Klasik bulgulan retinatla anjiomlar ve serebellumda hemanjioblastomlardır.

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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
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von Hippel-Lindau disease: surveillance strategy for endolymphatic sac tumors

, 2011
: Up to 16% of patients with the hereditary von Hippel-Lindau disease develop endolymphatic sac tumors of the inner ear. Early diagnosis and treatment of endolymphatic sac tumors can prevent audiovestibular morbidity, but optimal endolymphatic sac tumor ...
Poulsen, Marie Louise Mølgaard, Brandt, Carsten Alfred, Marie Louise Mølgaard Poulsen, Marie Luise Bisgaard, Møller, Hans Ulrik, Michael Kosteljanetz, Gimsing, Steen, Hans Ulrik Møller, Bisgaard, Søs Marie Luise, Carsten Alfred Brandt, Thomsen, Carsten, Kosteljanetz, Michael, Steen Gimsing, Carsten Thomsen   +13 more
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Familial CNS Tumor Syndromes: Von Hippel-Lindau Disease

, 2017
Von Hippel-Lindau disease can be inherited or may be caused by a spontaneous mutation. Individuals diagnosed with this disease are prone to developing multiple benign tumors termed hemangioblastomas.
Gurvinder Kaur, Joseph Weiner, Aruna Ganju, Leonel Ampie   +3 more
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Non‐expression of von Hippel‐Lindau phenotype in an obligate gene carrier

, 1994
Von Hippel‐Lindau disease is generally considered to be a condition with very high penetrance, and individuals who live beyond the age of 60 years without showing any features of the disease, despite undoubtedly carrying the gene defect, have not ...
D. G. R. Evans, Norman, A. M., Evans, D. G.R.; id_orcid, D. R. Davies, A. M. Norman, Whitehouse, R. W., R. W. Whitehouse, Davies, D. R.   +7 more
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Enfermedad de Von Hippel-Lindau: una presentación atípica [PDF]

, 2004
OBJETIVO: Describir una presentación atípica de la enfermedad de von Hippel-Lindau. MATERIAL Y MÉTODO: Presentamos la clínica, diagnóstico y tratamiento de las manifestaciones urológicas de esta enfermedad, de índole mayormente neurológica, en un varón ...
Murio,E., Abascal Junquera,J.M., Morote Robles,J., Trilla Herrera,E., Ramírez Sevilla,C., Serrallach Orejas,F., Esquena Fernández,S., Martos Calvo,R., M´Hammed,Y. Id, Torres,I. de   +9 more
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Masive enterorrhagia in patients suffering from hippel-lindau disease

Acta Médica del Centro, 2008
The Von Hippel Lindau disease is an autosomic-dominant neoplasia syndrome produced by a delection or mutation of tumor suppressor gene of chromosome 3p25. It was descripted by the German pathologist Arvid Lindau and the ophthalmologist Eugene Von Hippel,
Jorge Luis González Jara, Oliver Martín García, Gustavo A. Pérez Zavala   +2 more
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