Zobrazeno 1 - 10
of 17
pro vyhledávání: '"C E M Hillier"'
Publikováno v:
Child's Nervous System. 19:837-840
The authors present the case of a 31-year-old man with a malignant glioma. He had been treated for cerebral hydatid as a child, and 22 years later he developed a glioma at the site of his previous disease. Could chronic inflammatory change following
Autor:
C E M Hillier, N D Hawkes, G A O Thomas, I N F McQueen, G Shortland, A Jurewicz, O M Williams
Publikováno v:
Postgraduate Medical Journal. 77:717-722
The clinical syndrome of encephalopathy is most often encountered in the context of decompensated liver disease and the diagnosis is usually clear cut. Non-hepatic causes of encephalopathy are rarer and tend to present to a wide range of medical spec
Publikováno v:
QJM. 91:677-680
Fifteen patients with cerebral venous thrombosis were ascertained retrospectively. Their case notes were reviewed, and stored or new blood was assayed for factor V Leiden (FVL) mutation, prothrombin gene mutation 20201A, and 5,10 methylene tetrahydro
Autor:
R. B. Johanson, C. E. M. Hillier
Publikováno v:
International Journal of Gynecology & Obstetrics. 47:109-114
Objectives: To ascertain which instruments are most commonly used for assisted vaginal delivery. Methods: A postal survey in which 1411 questionnaires were sent to major obstetric centers worldwide. Results: Over 60% (305/508) of the respondents indi
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 72(3)
Objectives: To predict the size of the vCJD epidemic it is important to know whether the description of cases of vCJD in 1996 represent the first cases of a new disease entity or whether detection was due to increased surveillance of CJD in humans. D
To date there have been 52 reported cases of variant Creutzfeldt-Jakob disease (vCJD) in the United Kingdom. All cases that have undergone genetic investigation have been methionine homozygotes at codon 129 in the prion protein (PrP) gene. There has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8549b915024368d9ff6720e7b24ddf30
https://europepmc.org/articles/PMC1763448/
https://europepmc.org/articles/PMC1763448/
Autor:
R. L. Salmon, C. E. M. Hillier
Publikováno v:
QJM : monthly journal of the Association of Physicians. 93(9)
The transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative diseases of unknown aetiology, and affect both animals and man. As a group, they have several unique features that separate them from other neurodegenerative conditions,
The case described by Weetman et al 1 confirms the difficulty in managing drug induced (tardive) dyskinesia and dystonia, and suggests that posteroventral pallidotomy should be considered as a possible treatment option for this condition. We report o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9ec298b7a7a8ca517ef2f5a7e9eceb4
https://europepmc.org/articles/PMC1736211/
https://europepmc.org/articles/PMC1736211/
A patient with symptoms and signs of lumbar canal stenosis showed non-malignant, nerve root hypertrophy on MRI. The patient responded dramatically but temporarily to intravenous immunoglobulin (IVIg). Hypertrophy of nerve roots is recognised as a cau
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4611a022a3d905fbada6c2064480ba4d
https://europepmc.org/articles/PMC2170344/
https://europepmc.org/articles/PMC2170344/