Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Lower motor neuron involvement"'
Publikováno v:
Human Physiology. 46:900-911
Although multiple clinical trials of various therapeutic interventions in amyotrophic lateral sclerosis (ALS) have been conducted so far, most of them lack comprehensive study design due to the absence of progression biomarkers that could provide ade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef7362885003ae0730726cfb65f72569
https://doi.org/10.1134/s0362119720080010
https://doi.org/10.1134/s0362119720080010
Autor:
Sara C. Madeira, Julian Grosskreutz, Manuel Figueiral, Susana Pinto, Michael Swash, Magdalena Kuzma-Kozakiewicz, Marta Gromicho, Susanne Petri, Mamede de Carvalho, Hilmi Uysal
Publikováno v:
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 7, Iss 7, Pp 1181-1192 (2020)
Annals of Clinical and Translational Neurology, Vol 7, Iss 7, Pp 1181-1192 (2020)
© 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-No
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fe9164a38dd10c25b39036f94c406fc
http://europepmc.org/articles/PMC7359118
http://europepmc.org/articles/PMC7359118
Autor:
Ilaria Martinelli, Elisabetta Zucchi, Viviana Pensato, Cinzia Gellera, Bryan J Traynor, Giulia Gianferrari, Adriano Chiò, Jessica Mandrioli
Mutations in FUS gene have been described classically in young ALS patients with aggressive disease course. Here we report a large family carrying a missense mutation c.1520 GA in FUS gene with a tight association with an atypical FUS-ALS phenotype.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2aea23be349ad2361582cb205157cd3
https://hdl.handle.net/2318/1880714
https://hdl.handle.net/2318/1880714
Autor:
Ali Emre Oge, Bahar Erbas, Hava Özlem Dede, Emel Oguz Akarsu, Elif Kocasoy Orhan, Nermin Gorkem Sirin, Halil Atilla Idrisoglu, Mehmet Baris Baslo
Publikováno v:
Clinical Neurophysiology. 131:96-105
Objective To extract insight about the mechanism of repeater F-waves (Frep) by exploring their correlation with electrophysiologic markers of upper and lower motor neuron dysfunction in amyotrophic lateral sclerosis (ALS). Methods The correlations of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b896ab681dcf1d79a39ee28a0036ec32
https://doi.org/10.1016/j.clinph.2019.09.030
https://doi.org/10.1016/j.clinph.2019.09.030
Akademický článek
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Autor:
Corrado Angelini, Gabriele Siciliano
Introduction: Amyotrophic Lateral Sclerosis is a group of sporadic or familial disorders, characterized by upper and lower motor neuron involvement, with variable progression.Areas covered: The aut...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44b18bf62f485b70184da0d3e8e74af2
http://hdl.handle.net/11568/1141356
http://hdl.handle.net/11568/1141356
Autor:
Vincenzo Silani, Matthew C. Kiernan, Martin R Turner, Leonard H. van den Berg, Richard J. Barohn, John K. Fink, Jeffrey Statland, Hiroshi Mitsumoto, John Ravits, Philippe Corcia, Matthew B. Harms, Zachary Simmons
Publikováno v:
Journal of Neurology, Neurosurgery, and Psychiatry
Primary lateral sclerosis (PLS) is a neurodegenerative disorder of the adult motor system. Characterised by a slowly progressive upper motor neuron syndrome, the diagnosis is clinical, after exclusion of structural, neurodegenerative and metabolic mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af938d0d32f0750edac84a143b96259c
https://ora.ox.ac.uk/objects/uuid:2920aa43-6512-4782-8ad6-b3296ce33561
https://ora.ox.ac.uk/objects/uuid:2920aa43-6512-4782-8ad6-b3296ce33561
Publikováno v:
Journal of Electromyography and Kinesiology. 61:102606
The aim of this study was to evaluate the involvement of a peripheral motor neuron in Parkinson Disease (PD) using the motor unit number estimation (MUNE) method, which reflects motor unit loss in motor neuron diseases. Multipoint incremental MUNE me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::536acc232f2ca384f7b31b8305cd4b75
https://doi.org/10.1016/j.jelekin.2021.102606
https://doi.org/10.1016/j.jelekin.2021.102606
Publikováno v:
Muscle & Nerve. 54:378-385
Introduction The contribution of cranial and thoracic region electromyography (EMG) to diagnostic criteria for amyotrophic lateral sclerosis (ALS) has not been evaluated. Methods Clinical and EMG data from each craniospinal region were retrospectivel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26cdc1821a7fa9e38596ac819601c295
https://doi.org/10.1002/mus.25062
https://doi.org/10.1002/mus.25062
Autor:
Elif Kocasoy-Orhan, Mehmet Baris Baslo, Hava Özlem Dede, Halil Atilla Idrisoglu, Nermin Gorkem Sirin
Publikováno v:
Noro Psikiyatr Ars
INTRODUCTION: The present study is an examination of possible subclinical involvement of lower motor neuron (LMN) in patients with primary lateral sclerosis (PLS) and hereditary spastic paraparesis (HSP) electrophysiologically. METHODS: Nine PLS pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e30bfc515bd9cf235e700f5b6a1f0781
https://doi.org/10.29399/npa.23387
https://doi.org/10.29399/npa.23387