Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Dirk, Bäumer"'
Autor:
Janev, Fehmi, Alexander J, Davies, Jon, Walters, Timothy, Lavin, Ryan, Keh, Alexander M, Rossor, Tudor, Munteanu, Norman, Delanty, Rhys, Roberts, Dirk, Bäumer, Graham, Lennox, Simon, Rinaldi
Publikováno v:
Journal of neurology, neurosurgery, and psychiatry. 92(10)
We aimed to define the clinical and serological characteristics of pan-neurofascin antibody-positive patients.We tested serum from patients with suspected immune-mediated neuropathies for antibodies directed against nodal/paranodal protein antigens u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01938a44d5c2df1da15b24f784d59826
https://pubmed.ncbi.nlm.nih.gov/34400541
https://pubmed.ncbi.nlm.nih.gov/34400541
Autor:
Graham G Lennox, Tudor Munteanu, Ryan Keh, Norman Delanty, Alexander J. Davies, Rhys C. Roberts, Janev Fehmi, Jon Walters, Alexander M. Rossor, Timothy Lavin, Simon Rinaldi, Dirk Bäumer
ObjectivesWe aimed to define the clinical and serological characteristics of pan-neurofascin antibody-positive patients.MethodsWe tested serum from patients with suspected immune-mediated neuropathies for antibodies directed against nodal/paranodal p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::237d54e0602cbddba3b6c038db33eb26
https://doi.org/10.1101/2021.01.29.21250485
https://doi.org/10.1101/2021.01.29.21250485
Autor:
Dirk Bäumer, Sheena Lee, George Nicholson, Joanna L Davies, Nicholas J Parkinson, Lyndsay M Murray, Thomas H Gillingwater, Olaf Ansorge, Kay E Davies, Kevin Talbot
Publikováno v:
PLoS Genetics, Vol 5, Iss 12, p e1000773 (2009)
Spinal muscular atrophy is a severe motor neuron disease caused by inactivating mutations in the SMN1 gene leading to reduced levels of full-length functional SMN protein. SMN is a critical mediator of spliceosomal protein assembly, and complete loss
Externí odkaz:
https://doaj.org/article/65c68e49f26e4562805f2aa303b74144
Autor:
Dirk Bäumer
Publikováno v:
Oxford Medicine
It is not always clear that a symptom is due to a problem in the nervous system. Delirium, generalized weakness, and fatigue are frequently due to systemic illness. Transient loss of consciousness may have a neurological or cardiac cause. It is, ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98d763ae15f6599287f696905de9c3b3
https://doi.org/10.1093/med/9780199568741.003.0220
https://doi.org/10.1093/med/9780199568741.003.0220
Autor:
Dirk Bäumer
Publikováno v:
Oxford Medicine
A basic understanding of the anatomy and physiology of the nervous system function is necessary to understand and diagnose neurological disease. This chapter will give a brief outline of those aspects of neuroanatomy and neurophysiology which are hel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e77e71950d8a2b9b0f997c2b40067d4c
https://doi.org/10.1093/med/9780199568741.003.0219
https://doi.org/10.1093/med/9780199568741.003.0219
Autor:
Dirk Bäumer
Seizures are transient neurological events caused by abnormal excessive or synchronous neuronal activity in the brain. This can arise from a localized brain region, causing focal seizures, or simultaneously from both hemispheres, leading to generaliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82a7a5700f7f0528b908f6713612d03b
https://doi.org/10.1093/med/9780199568741.003.0042
https://doi.org/10.1093/med/9780199568741.003.0042
Autor:
Simon Hammans, Dirk Bäumer
Publikováno v:
British Journal of Hospital Medicine. 76:576-582
Patients with muscle disease present not only to neurologists, but also to rheumatologists and general physicians. This article provides a framework of how to approach patients with suspected muscle disease, and reviews the clinical features of the m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2d08a739be3ac2b6bdd7a1ff320d70c
https://doi.org/10.12968/hmed.2015.76.10.576
https://doi.org/10.12968/hmed.2015.76.10.576
Publikováno v:
Practical neurology. 17(4)
Enterovirus D68 has been associated with a poliomyelitis-like illness, notably during an outbreak in 2014, and particularly affecting children in the USA. We report a case of acute segmental flaccid paralysis with respiratory involvement in an adult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::692494ad228d56c173052fa98db49859
https://pubmed.ncbi.nlm.nih.gov/28626021
https://pubmed.ncbi.nlm.nih.gov/28626021
Publikováno v:
Acta Neuropathologica. 128:597-604
Polyglutamine expansions in the ataxin-2 gene (ATXN2) cause autosomal dominant spinocerebellar ataxia type 2 (SCA2), but have recently also been associated with amyotrophic lateral sclerosis (ALS). We present clinical and pathological features of a f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae6f61cf92bbe90de341cb0a32d3e070
https://doi.org/10.1007/s00401-014-1277-z
https://doi.org/10.1007/s00401-014-1277-z
Publikováno v:
Journal of the Royal Society of Medicine. 107:14-21
Summary Motor neurone disease (MND), the commonest clinical presentation of which is amyotrophic lateral sclerosis (ALS), is regarded as the most devastating of adult-onset neurodegenerative disorders. The last decade has seen major improvements in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0891b35cfdac638cad44d5aa45c280d
https://doi.org/10.1177/0141076813511451
https://doi.org/10.1177/0141076813511451