Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Stephan R. Jaiser"'
Autor:
Besa Ziso, Tim L. Williams, R. Jon L. Walters, Stephan R. Jaiser, Johannes Attems, Udo C. Wieshmann, A.J. Larner, Anu Jacob
Publikováno v:
Case Reports in Neurology, Vol 7, Iss 1, Pp 95-100 (2015)
Three patients with the clinical and investigation features of facial onset sensory and motor neuronopathy (FOSMN) syndrome are presented, one of whom came to a post-mortem examination. This showed TDP-43-positive inclusions in the bulbar and spinal
Externí odkaz:
https://doaj.org/article/0c3dab9727c64f369c0444f966e5b807
Autor:
Cameron J. Williams, Kevin J. Wilson, Stephan R. Jaiser, Nina Wilson, Timothy L. Williams, Mark R. Baker
Background Motor neurone disease (MND) is a rapidly progressing and rare neurodegenerative disorder characterized by progressive weakness, muscle wasting, and death from respiratory failure within 36 months of symptom onset. To date, clinical trials
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae811f80b0a866791e98407b75e4c4cd
https://doi.org/10.21203/rs.3.rs-2493177/v1
https://doi.org/10.21203/rs.3.rs-2493177/v1
Publikováno v:
Epileptic disorders : international epilepsy journal with videotape. 24(5)
Autor:
Hugo M. De Oliveira, Matthew Silsby, Stephan R. Jaiser, H. Ming Lai, Nathan Pavey, Matthew C. Kiernan, Tim L. Williams, Steve Vucic, Mark R. Baker
Publikováno v:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 140
To determine the electrodiagnostic characteristics of facial onset sensory and motor neuronopathy (FOSMN).Electrophysiological data from 10 FOSMN patients in Newcastle-upon-Tyne and Sydney were reviewed. Relevant literature was reviewed.Findings on s
Publikováno v:
Journal of Neurology
Mills’ syndrome is an idiopathic, slowly progressive, spastic hemiparesis. We describe three cases that have been under review for a minimum of 11 years (range 11–19). In all patients, symptoms started in a leg, with a mean age of onset of 59 yea
Autor:
Stephan R. Jaiser, Hannah E. Steele, Michael J. Keogh, Patrick F. Chinnery, Mark R. Baker, Rita Horvath
Publikováno v:
Neurology: Clinical Practice. 7:451-454
The clinical scenario of a woman aged 30–50 years presenting with progressive lower limb spasticity, asymmetric changes on visual evoked potentials (VEPs), somatosensory evoked potentials (SEPs), and motor evoked potentials (MEPs) consistent with c
Publikováno v:
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 129(7)
Autor:
R. Jon Walters, Besa Ziso, Andrew J Larner, Anu Jacob, Tim Williams, U. C. Wieshmann, Johannes Attems, Stephan R. Jaiser
Publikováno v:
Case Reports in Neurology, Vol 7, Iss 1, Pp 95-100 (2015)
Case Reports in Neurology
Case Reports in Neurology
Three patients with the clinical and investigation features of facial onset sensory and motor neuronopathy (FOSMN) syndrome are presented, one of whom came to a post-mortem examination. This showed TDP-43-positive inclusions in the bulbar and spinal
Autor:
Stephan R. Jaiser, Gavin P. Winston
Publikováno v:
Seizure. 21:371-376
Purpose To review the legislation for non-commercial driving licenses in the Western world for unprovoked first seizures (UFS) and recurrence of established epilepsy, and to examine available evidence on the road traffic accident (RTA) risk in people
Autor:
Gavin P. Winston, Stephan R. Jaiser
Publikováno v:
Journal of Neurology
Acquired copper deficiency has been recognised as a rare cause of anaemia and neutropenia for over half a century. Copper deficiency myelopathy (CDM) was only described within the last decade, and represents a treatable cause of non-compressive myelo