Zobrazeno 1 - 10
of 114
pro vyhledávání: '"T, Ansved"'
Autor:
T. Ansved, Peter J. Radell, Katarina Fredriksson, Olav Rooyackers, G. Måbäck, K. Ahlbeck, S. Remahl, Lars Eriksson
Publikováno v:
Acta Anaesthesiologica Scandinavica. 53:717-723
Background: Critical illness polyneuropathy and myopathy (CIPNM) is recognized as a common condition that develops in the intensive care unit (ICU). It may lead to a prolonged hospital stay with subsequent increased ICU and hospital costs. Knowledge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc90a425d71bac463d24f18975ff20b
https://doi.org/10.1111/j.1399-6576.2009.01952.x
https://doi.org/10.1111/j.1399-6576.2009.01952.x
Publikováno v:
Acta Neurologica Scandinavica. 96:266-270
Three Swedish patients with proximal muscle weakness, myotonia and lack of CTG expansion on genetical analysis are presented. Clinical neurological and neurophysiological examination and muscle biopsy were performed. There was an indication of autoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ff08b76c48660a89ee137ae74a1b5ca
https://doi.org/10.1111/j.1600-0404.1997.tb00282.x
https://doi.org/10.1111/j.1600-0404.1997.tb00282.x
Publikováno v:
Acta Neurologica Scandinavica. 112:223-227
Objectives – To characterise a Swedish family with a rare hereditary myopathy with unique sarcoplasmic inclusion bodies in the muscle biopsy. Materials and methods – Part of the pedigree was described in 1980. Nine new members of the included and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d25310d3b839d08660262ce5ea322c98
https://doi.org/10.1111/j.1600-0404.2005.00475.x
https://doi.org/10.1111/j.1600-0404.2005.00475.x
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 75:917-920
Objective: To characterise morphological abnormalities in relation to muscle fibre type in sporadic inclusion body myositis (s-IBM). Methods: 14 muscle biopsies from 11 patients with s-IBM were characterised for morphological abnormalities and fibre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b2fcb45dcd1d9ffacf5bd265fced47f
https://doi.org/10.1136/jnnp.2003.018994
https://doi.org/10.1136/jnnp.2003.018994
Autor:
T Ansved
Publikováno v:
Acta Physiologica Scandinavica. 171:359-366
There has been a debate for many years on whether muscular training is beneficial or harmful for patients with myopathic disorders and the role of exercise training in the management of these patients is still controversial. Much of this confusion is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6423395831f9d83578a56be901a3bd3
https://doi.org/10.1046/j.1365-201x.2001.00839.x
https://doi.org/10.1046/j.1365-201x.2001.00839.x
Publikováno v:
Acta Neurologica Scandinavica. 103:131-135
We report a 73-year-old woman with sporadic inclusion body myositis (s-IBM) and a T-cell chronic lymphocytic leukaemia (T-CLL). The s-IBM diagnosis was based on clinical symptoms and muscle biopsy showing inflammatory infiltrates and rimmed vacuoles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd20affa74438d0d2acbf2df855732ef
https://doi.org/10.1034/j.1600-0404.2001.103002131.x
https://doi.org/10.1034/j.1600-0404.2001.103002131.x
Autor:
Thomas A. Cooper, H. Jaeger, D. Furutama, M. Siciliano, Giovanni Antonini, Geneviève Gourdon, S. Michalowski, E. Eddy, R. Krahe, John W. Day, S. E. Harris, J. P. Barbet, M. Shimizu, G. B. Browne, M. Gosling, A. V. Philips, Loreto Martorell, P. Maire, Glenn E. Morris, Zeljka Korade, N. Carey, Richard R. Sinden, C. A. Thornton, A. M. Mitchell, M. Baiget, A. Balasubramanyam, L. P.W. Ranum, Shigeru Sato, M. Eriksson, T. Kobayashi, M. Khajavi, J. Mathieu, F. K. Gould, B. Eymard, D. Pribnow, R. H. Singer, J. D. Griffith, C. Liquori, M. Wagner, T. Ansved, D. E. Housman, N. Spring, A. Johansson, S. Salvatori, B. Luciano, Claudia Abbruzzese, I. Gonzales, J. Adelman, J. P. Mounsey, B. Wieringa, J. Waring, B. Perryman, D. Furling, M. Devillers, H. Furuya, F. Lehmann, H. Yamagata, M. S. Mahadevan, Darren G. Monckton, Geoffrey P. Miller, D. Hilton Jones, A. S. Lia-Baldini, J. Westerlaken, M. Swanson, S. J. Tapscott, T. R. Klesert, R. D. Wells, N. Ohsawa, H. Seznec, H. Moore, E. J. Chen, M. Hamshere, Tetsuo Ashizawa, U. Kvist, A. D. Roses, C. Junien, Catherine L Winchester, M. Gennarelli, M. Kinoshita, K. Johnson, Christopher E. Pearson, Lubov Timchenko, J. R. Moorman
Publikováno v:
Neurology. 54:1218-1221
Myotonic dystrophy (DM; OMIM 160900, also known as dystrophia myotonica, myotonia atrophica and Steinert disease) is an autosomal dominant myotonic myopathy associated with abnormalities of other organs, including eyes, heart, endocrine system, centr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05f05337336afd1fbc3491f94730a7cf
https://doi.org/10.1212/wnl.54.6.1218
https://doi.org/10.1212/wnl.54.6.1218
Autor:
L-E, Thornell, M, Lindstöm, V, Renault, A, Klein, V, Mouly, T, Ansved, G, Butler-Browne, D, Furling
Publikováno v:
Neuropathology and applied neurobiology. 35(6)
Myotonic dystrophy type 1 (DM1), one of the most common forms of inherited neuromuscular disorders in the adult, is characterized by progressive muscle weakness and wasting leading to distal muscle atrophy whereas proximal muscles of the same patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5be47e1fbb3e9e14f1fdc7517525e6dd
https://pubmed.ncbi.nlm.nih.gov/19207265
https://pubmed.ncbi.nlm.nih.gov/19207265
Publikováno v:
Acta Physiologica Scandinavica. 143:345-354
The spatial arrangement and morphometrical properties of the muscle fibres within single motor units (motor unit fibres) were studied in fast-twitch units of the tibialis anterior (TA) and in slow-twitch units of the soleus, using a computer-assisted
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ae234dfd1a550bfe5fc778e2cdd4889
https://doi.org/10.1111/j.1748-1716.1991.tb09242.x
https://doi.org/10.1111/j.1748-1716.1991.tb09242.x
Publikováno v:
Acta anaesthesiologica Scandinavica. 48(4)
Background: Despite a similar density of nicotinic acetylcholine receptors, the upper esophageal sphincter is sensitive to partial neuromuscular block, whereas the pharyngeal constrictor muscle is more resistant. In order to postulate possible mechan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cdf9683899f7a2e7178131ca12d49f2
https://pubmed.ncbi.nlm.nih.gov/15025603
https://pubmed.ncbi.nlm.nih.gov/15025603