Zobrazeno 1 - 10 of 23 pro vyhledávání: '"R J Swingler"'
1
Cause of death and clinical grading criteria in a cohort of amyotrophic lateral sclerosis cases undergoing autopsy from the Scottish Motor Neurone Disease Register
Autor: R J Swingler, Shuna Colville, Raeburn B Forbes, Kathreena M Kurian
Publikováno v: Journal of Neurology, Neurosurgery & Psychiatry. 80:84-87
Background: The Scottish Motor Neurone Disease Register is a population based register of amyotrophic lateral sclerosis/motor neurone disease (ALS/MND) in Scotland, with high case ascertainment levels. Objective: To investigate the cause of death by
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8faae47b5f855d77235b8983bb9b60a7
https://doi.org/10.1136/jnnp.2008.149708
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2
Motor Neuron Diseasea Review
Autor: J Pritchard, R J Swingler
Publikováno v: Scottish Medical Journal. 45:4-7
It is now clear that patients with MND are best managed using a multi-disciplinary approach conforming to evidence-based guidelines. Whilst scientific advances into the aetiology of MND have been of great importance in both the understanding of this
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::432233935d377592c949df8abbe67808
https://doi.org/10.1177/003693300004500102
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3
Not hysteria: ovarian teratoma-associated anti-N-methyl-D-aspartate receptor encephalitis
Autor: P O'Brien, N J J MacDougall, R Roberts, J Christie, K Abdelaziz, R J Swingler
Publikováno v: Scottish medical journal. 57(3)
We report a case of a 33-year-old nulliparous woman who, following a short prodromal illness, experienced a series of psychiatric and behavioural symptoms. These included states of terror, insomnia, delirium, self-harm and suicidal ideation, facial d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ee710dfb3b887d3f14833aec0f09685
https://pubmed.ncbi.nlm.nih.gov/22859813
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4
Western blotting analysis in patients with MS using human brain vessels as antigen
Autor: R. J. Swingler, D. L. W. Davidson, R. E. Cull, Shannon Atkinson, J. E. Bell, JM Anderson, W. C. Russell, I. Davison, B. E. Souberbielle
Publikováno v: Acta Neurologica Scandinavica. 86:397-402
Serum samples from patients suffering from multiple sclerosis, other neurological diseases and normal controls were screened by "western blotting" for antibody directed against proteins of human brain vessels purified from a post mortem brain. A smal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5364102adb2df30dbb6bdea3a781812f
https://doi.org/10.1111/j.1600-0404.1992.tb05107.x
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5
Peripheral neuropathy simulating lymphoma
Autor: R. E. Cull, D. Kean, L. Turnbull, R. J. Swingler
Publikováno v: The British Journal of Radiology. 65:344-347
Nerve hypertrophy occurs in some types of Charcot-Marie-Tooth syndrome (hereditary motor and sensory neuropathy (HMSN) type I), Dejerine-Sottas disease (HMSN type III), Refsum's disease (HMSN type IV), neurofibromatosis, amyloidosis, sarcoidosis, lep
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d54c2d044848c5a78fe75541d94ca4d
https://doi.org/10.1259/0007-1285-65-772-344
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6
Rapid mutation detection by the Transgenomic wave analyser DHPLC identifies MYOC mutations in patients with ocular hypertension and/or open angle glaucoma
Autor: R J Swingler, J Ellis, G Scott, Caroline Cobb, S Wilson, Whi McLean, C J MacEwen
Aims: To rapidly screen Scottish patients with a family history of open angle glaucoma (OAG) or ocular hypertension (OHT) for mutations in the myocilin gene (MYOC) and develop a new rapid screening method for MYOC mutation detection. Methods: All thr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::762067a946c9ad406bd9ddc1a8efaa24
https://europepmc.org/articles/PMC1771000/
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7
Clinical heterogeneity of familial motor neuron disease: report of 11 pedigrees from a population based study in Scotland. The Scottish Motor Neuron Disease Research Group
Autor: A M, Chancellor, H, Fraser, R J, Swingler, S M, Holloway, C P, Warlow
Publikováno v: Journal of the neurological sciences.
Five percent of incident patients with MND in Scotland 1989-1990 had a family history of this disease. This paper assesses the demographic and clinical features of this group.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ccdbf28b5e9ec4cdc1c20372c23bb8ba
https://pubmed.ncbi.nlm.nih.gov/7807151
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9
Utility of Scottish morbidity and mortality data for epidemiological studies of motor neuron disease
Autor: A M Chancellor, R J Swingler, C P Warlow, J A Clarke, H Fraser
OBJECTIVES--To determine the accuracy of (1) hospital discharge data and (2) death certificates, coded as motor neuron disease (MND). DESIGN--Comparison of data from The Scottish Motor Neuron Disease Register (SMNDR) with routinely collected Scottish
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2008dc8b0b9dbae164c31999811b412d
https://europepmc.org/articles/PMC1059738/
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10
The prognosis of motor neurone disease
Autor: R J Swingler
Publikováno v: Journal of Neurology, Neurosurgery & Psychiatry. 81:1062-1062
It has recently been argued that people with motor neurone disease (MND) are living longer because of improvements in symptomatic care.1 However, this conclusion is based on an analysis of selected patients recruited into the placebo arm of trials. P
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e8a7caea5bf3557b3b87ef2bcc4673d8
https://doi.org/10.1136/jnnp.2010.206888
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