Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Hirayama's disease"'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Case Reports in Neurology, Vol 12, Iss 3, Pp 291-298 (2020)
Hirayama disease is a rare neurological entity that is characterized by initial progressive muscular wasting and weakness of the distal upper limb in young men, followed by a spontaneous arrest within several years. The disease is believed to be a re
Externí odkaz:
https://doaj.org/article/219706550cce443f91958d09dee056d4
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 9, Iss 3, Pp 61-65 (2017)
Monomelic amyotrophy (MMA) is a rare variant of lower motorneuron disease with benign progression. The disease is characterizedby muscular weakness and atrophy in the hand and forearmon one side or asymmetrical lesion of both upper limbs with thepres
Externí odkaz:
https://doaj.org/article/2a14ea9f4dd245de9859ef57dc3d0b3a
Publikováno v:
Case Reports in Neurology
Case Reports in Neurology, Vol 12, Iss 3, Pp 291-298 (2020)
Case Reports in Neurology, Vol 12, Iss 3, Pp 291-298 (2020)
Hirayama disease is a rare neurological entity that is characterized by initial progressive muscular wasting and weakness of the distal upper limb in young men, followed by a spontaneous arrest within several years. The disease is believed to be a re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaf5eec93c8cf28849a5b163c14fb987
http://europepmc.org/articles/PMC7549014
http://europepmc.org/articles/PMC7549014
Publikováno v:
Advanced Biomedical Research, Vol 6, Iss 1, Pp 95-95 (2017)
Hirayama's disease is a rare clinical variant of amyotrophic lateral sclerosis where distal muscles are involved more compared to proximal muscles and vice-versa occurs only in 10% cases and so it is differentiated from O'Sullivan McLeod syndrome whi
Externí odkaz:
https://doaj.org/article/4aecddd5e3d54c8a9d742b01e97aaaa9
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Fiore Manganelli, Arturo Brunetti, Ferdinando Caranci, Francesco Briganti, Chiara Pisciotta, Lucio Santoro, Valerio Vitale
Publikováno v:
Quantitative Imaging in Medicine and Surgery. 6:364-373
Background Hirayama's disease (HD), is a benign, self-limited, motor neuron disease, characterized by asymmetric weakness and atrophy of one or both distal upper extremities. In the present study we report the clinical, electrophysiological and MRI f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::330d44cfbe33b35cf14451c2a6d30fb0
https://doi.org/10.21037/qims.2016.07.08
https://doi.org/10.21037/qims.2016.07.08
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Journal of Orthopaedic Case Reports, Vol 3, Iss 3, Pp 11-14 (2013)
Journal of Orthopaedic Case Reports
Journal of Orthopaedic Case Reports
Introduction: Hirayama’s disease is a rare benign disorder, also referred to as monomelic amyotrophy (MMA), Juvenile non progressive amyotrophy, Sobue disease. It is a focal, lower motor neuron type of disease. Mainly young males in their second an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6829c1b81e5d2f0b0874ab1f193399a
https://doi.org/10.13107/jocr.2250-0685.107
https://doi.org/10.13107/jocr.2250-0685.107
Publikováno v:
Advanced Biomedical Research, Vol 6, Iss 1, Pp 95-95 (2017)
Advanced Biomedical Research
Advanced Biomedical Research
Hirayama's disease is a rare clinical variant of amyotrophic lateral sclerosis where distal muscles are involved more compared to proximal muscles and vice-versa occurs only in 10% cases and so it is differentiated from O’Sullivan McLeod syndrome w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbe3677642ca9be2006b2ee64cb1be57
https://doi.org/10.4103/2277-9175.211797
https://doi.org/10.4103/2277-9175.211797