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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Cognitive deficits in myopathies

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Auteur
Peristeri E., Aloizou A.-M., Keramida P., Tsouris Z., Siokas V., Mentis A.-F.A., Dardiotis E.
Date
2020
Language
en
DOI
10.3390/ijms21113795
Sujet
clinical feature
clinical observation
cognitive defect
disease classification
Duchenne muscular dystrophy
endocrine related myopathy
frontotemporal dementia
genetic disorder
human
information retrieval
Medline
mitochondrial myopathy
myopathy
myotonic dystrophy
neuroimaging
Paget bone disease
Review
Scopus
brain
classification
cognitive defect
complication
diagnostic imaging
genetics
pathophysiology
Brain
Cognitive Dysfunction
Humans
Muscular Dystrophy, Duchenne
Myotonic Dystrophy
MDPI AG
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Résumé
Myopathies represent a wide spectrum of heterogeneous diseases mainly characterized by the abnormal structure or functioning of skeletal muscle. The current paper provides a comprehensive overview of cognitive deficits observed in various myopathies by consulting the main libraries (Pubmed, Scopus and Google Scholar). This review focuses on the causal classification of myopathies and concomitant cognitive deficits. In most studies, cognitive deficits have been found after clinical observations while lesions were also present in brain imaging. Most studies refer to hereditary myopathies, mainly Duchenne muscular dystrophy (DMD), and myotonic dystrophies (MDs); therefore, most of the overview will focus on these subtypes of myopathies. Most recent bibliographical sources have been preferred. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
URI
http://hdl.handle.net/11615/78060
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]
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