Zobrazeno 1 - 10
of 19
pro vyhledávání: '"A.M. Saukkonen"'
Autor:
Sara Lehtinen, Anna Vihola, Sanna Huovinen, Bjarne Udd, A.M. Saukkonen, Johanna Palmio, Manu Jokela
Publikováno v:
Journal of Neurology
Limb-girdle muscular dystrophies (LGMD) are genetic disorders characterized by weakness of predominantly proximal limb and trunk muscles due to progressive loss of muscle tissue. Collagen VI-related muscular dystrophies usually display more generaliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faa483cc92bea37624161fdbbb77458c
Autor:
A.M. Saukkonen, Sini Penttilä, Johanna Palmio, Satu K. Jääskeläinen, Satu Sandell, Manu Jokela, Raija Soikkeli, Bjarne Udd
Publikováno v:
Journal of the Neurological Sciences. 355(1-2):143-146
There is limited data on electromyography (EMG) findings in other motor neuron disorders than amyotrophic lateral sclerosis (ALS). We assessed whether the distribution of active denervation detected by EMG, i.e. fibrillations and fasciculations, diff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::531addb92e320cd98cef802bc2b4d37c
http://juuli.fi/Record/0006681315
http://juuli.fi/Record/0006681315
Autor:
Sini Penttilä, Sanna Huovinen, J. Toivanen, Manu Jokela, Bjarne Udd, Peter Hackman, A.M. Saukkonen
Publikováno v:
Neurology. 77:334-340
Objective: Characterization of a new type of late-onset autosomal dominant lower motor neuron disease. Methods: Patients from 2 families underwent detailed neurologic, electrophysiologic, muscle biopsy, and laboratory investigations. MRI of lower lim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42cc746a3512ca52ebda47b2a3b0b9cb
https://doi.org/10.1212/wnl.0b013e3182267b71
https://doi.org/10.1212/wnl.0b013e3182267b71
Publikováno v:
Neuromuscular Disorders. 27(10):962-963
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::310b3688d383f0174b71ea32c181e83b
https://doi.org/10.1016/j.nmd.2017.06.014
https://doi.org/10.1016/j.nmd.2017.06.014
Publikováno v:
Epilepsy Research. 25:291-297
A new anti-epileptic drug, tiagabine, is a potent inhibitor of GABA uptake into neurons and glia. Tiagabine has shown promising efficacy and safety profiles as add-on treatment for partial seizures. We evaluated the long-term effects of tiagabine on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed57d61cf33f66cb1d8e85273a2542e0
https://doi.org/10.1016/s0920-1211(96)00084-8
https://doi.org/10.1016/s0920-1211(96)00084-8
Akademický článek
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Publikováno v:
Neuromuscular Disorders. 23:772
Spinal muscular atrophies (SMA) form a category of inherited motor neuron disorders that predominantly affect lower motor neurons. Different SMA types are clinically and genetically heterogeneous and many of them show significant phenotypic overlap.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d83a1f264cbbab3cf7d97494fc7c0e90
https://doi.org/10.1016/j.nmd.2013.06.479
https://doi.org/10.1016/j.nmd.2013.06.479
Publikováno v:
Neuromuscular Disorders. 22:871
Spinal muscular atrophies (SMA) are hereditary disorders characterized by degeneration of lower motor neurons. Different SMA types are clinically and genetically heterogeneous and many of them show significant phenotypic overlap. We have previously d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::885e622875da79ba431c88e57725c054
https://doi.org/10.1016/j.nmd.2012.06.227
https://doi.org/10.1016/j.nmd.2012.06.227
Publikováno v:
Neuromuscular Disorders. 21:684
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da7f785d2e73fd55ffaa01508e4fdeb4
https://doi.org/10.1016/j.nmd.2011.06.903
https://doi.org/10.1016/j.nmd.2011.06.903
Publikováno v:
Neuromuscular Disorders. 19:597
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dac82bf5c495aa593b26258d5321a9db
https://doi.org/10.1016/j.nmd.2009.06.170
https://doi.org/10.1016/j.nmd.2009.06.170