Zobrazeno 1 - 10
of 10
pro vyhledávání: '"C E Pringle"'
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0159993 (2016)
Immunoglobulin therapy has become a major treatment option in several autoimmune neuromuscular disorders. For patients with Myasthenia Gravis (MG), intravenous immunoglobulin (IVIg) has been used for both crisis and chronic management. Subcutaneous I
Externí odkaz:
https://doaj.org/article/51ec95dadd824fbfb212fd895b29bd3f
Publikováno v:
Archives of Neurology. 54:896-900
Background: The human T-cell lymphotropic virus type 1 (HTLV-1) is associated with a chronic, progressive myelopathy termedtropical spastic paraparesisorHTLV-1—associated myelopathy. An increasing number of reports suggest that the spectrum of neur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a7f8ab5d54dd9d2c1c024c2cc0618c5
https://doi.org/10.1001/archneur.1997.00550190084018
https://doi.org/10.1001/archneur.1997.00550190084018
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 8, p e0159993 (2016)
PLoS ONE, Vol 11, Iss 8, p e0159993 (2016)
Background Immunoglobulin therapy has become a major treatment option in several autoimmune neuromuscular disorders. For patients with Myasthenia Gravis (MG), intravenous immunoglobulin (IVIg) has been used for both crisis and chronic management. Sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81b9fd232c37957f8ae2f2e8aabcbb6a
https://doi.org/10.1371/journal.pone.0159993
https://doi.org/10.1371/journal.pone.0159993
Publikováno v:
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 20:184-193
A relationship between epilepsy and damage to mesial temporal structures has long been recognized. Recent advances have clarified somewhat the issue of whether the pathological changes seen in mesial temporal sclerosis represent the cause or the effe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09ecbda11f87f3cabb861e8dd087b10
https://doi.org/10.1017/s0317167100047910
https://doi.org/10.1017/s0317167100047910
Publikováno v:
Musclenerve. 20(3)
A 45-year-old man developed ophthalmoplegia and subsequently multiple cranial nerve palsies in association with bibrachial paresis. Investigations revealed evidence of conduction block occurring at a very proximal location (i.e., the spinal roots) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2d7c8066d7dd86b245baa008e99b59a7
https://pubmed.ncbi.nlm.nih.gov/9052814
https://pubmed.ncbi.nlm.nih.gov/9052814
Publikováno v:
Eye (London, England). 11
A 45-year-old Caucasian woman presented with sudden onset right-sided hemiparesis, aphasia and a painful left eye. Examination revealed a bone-white fundus with no perfusion of either the retinal or choroidal circulations. Magnetic resonance imaging
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51306dbcd0a0e2feb087dcd6dc18bf72
https://pubmed.ncbi.nlm.nih.gov/9246271
https://pubmed.ncbi.nlm.nih.gov/9246271
Autor:
William F. Brown, David G. Munoz, A J Hudson, C. E. Pringle, George C. Ebers, John A. Kiernan
Publikováno v:
Scopus-Elsevier
Primary lateral sclerosis (PLS) bears close resemblance to cases of amyotrophic lateral sclerosis (ALS) presenting with spasticity, but histopathological studies have shown significant difference between the two conditions. When the lower motor neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f243d8c9e6fb33480c874d24427a1870
https://pubmed.ncbi.nlm.nih.gov/8457884
https://pubmed.ncbi.nlm.nih.gov/8457884
Publikováno v:
Neurology. 46:585-586
Traditionally, ``knapsack palsy'' refers to a weakness of the serratus anterior muscle secondary to injury of the long thoracic nerve [1] consequent to carrying a heavy knapsack for a prolonged period. We recently encountered a patient who developed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9c0016cb31b40639cc626fe43a6a2d2
https://doi.org/10.1212/wnl.46.2.585
https://doi.org/10.1212/wnl.46.2.585
Autor:
A J Hudson, George C. Ebers, William F. Brown, David G. Munoz, C. E. Pringle, John A. Kiernan
Publikováno v:
Scopus-Elsevier
Eight patients with a homogeneous syndrome of progressive symmetric spinobulbar spasticity were studied. Clinical features were limited to those associated with dysfunction of the descending motor tracts and included spastic quadriparesis, pseudobulb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::891ed537c13ed8e837ea240d38069c0c
http://www.scopus.com/inward/record.url?eid=2-s2.0-0026682621&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0026682621&partnerID=MN8TOARS
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