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pro vyhledávání: '"R. Jon Walters"'
Autor:
Janev Fehmi, R Jon Walters, Tim Lavin, Ryan Keh, Alexander M Rossor, Tudor Munteanu, Norman Delanty, Rhys Roberts, Dirk Baumer, Simon Rinaldi
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 93:A1.1-A1
ImportanceDisease modifying treatments in Guillain-Barré syndrome (GBS) are not tailored to the different pathological subtypes. Strategies to prospectively identify sub-sets of patients with specific disease mecha- nisms and inform the use of non-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55c1e42af5732ebd27d687f91cd21f72
https://doi.org/10.1136/jnnp-2022-abn.1
https://doi.org/10.1136/jnnp-2022-abn.1
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a157ed104c46fbe7810373b78598e4d1
https://doi.org/10.1159/000381944
https://doi.org/10.1159/000381944
Autor:
Raquel Real, Ruth Lamb, Tammaryn Lashley, R. Jon Walters, Huw R. Morris, Adrian James Waite, Derek J. Blake, Steven J. Lubbe, Tamas Revesz, Jonathan D. Rohrer, Janice L. Holton
Publikováno v:
Molecular Case Studies. 5:a003913
Mutations in the TANK-binding kinase 1 (TBK1) gene have recently been shown to cause frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The phenotype is highly variable and has been associated with behavioral variant FTD, primary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4f275a66004f341391205d0b00f0fa5
https://doi.org/10.1101/mcs.a003913
https://doi.org/10.1101/mcs.a003913
Autor:
R Jon Walters
Publikováno v:
Practical neurology. 16(4)
Contractures are one of a handful of signs in muscle disease, besides weakness and its distribution, whose presence can help guide us diagnostically, a welcome star on the horizon. Contractures are associated with several myopathies, some with import
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030f70240edc92a88a9ffd1d00191177
https://pubmed.ncbi.nlm.nih.gov/26867558
https://pubmed.ncbi.nlm.nih.gov/26867558
Autor:
R Jon Walters
Publikováno v:
Practical neurology. 14(5)
Muscle diseases are not as common as headaches and funny turns in our general neurology clinics, but most of us will encounter them. We all pride ourselves on a methodical approach to clinical problems-discovering the where and what in neurological p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83f49f10fb7eea1a2dd5ef0a1aa4b450
https://pubmed.ncbi.nlm.nih.gov/24928573
https://pubmed.ncbi.nlm.nih.gov/24928573
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 86:e4.71-e4
Mitochondrial encephalomyelitis, lactic acidosis and stroke-like episodes (MELAS) syndrome is the most common of the rare mitochondrial disorders. It frequently is secondary to a point mutation in mitochondrial DNA m.3243 A to G. The main features of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5681d6d47bf163683415a647d49f7cb
https://doi.org/10.1136/jnnp-2015-312379.162
https://doi.org/10.1136/jnnp-2015-312379.162
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