Zobrazeno 1 - 10
of 36
pro vyhledávání: '"flexion mri"'
Autor:
Valentina Elisabetta Lolli, MD, MSc, Nicolae Sarbu, MD, PhD, Martina Pezzullo, MD, Nicolas Mavroudakis, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 15, Iss 9, Pp 1701-1704 (2020)
We report the case of an 18-year old male with a history of asymmetric weakness and amyotrophy of distal upper extremities, suggestive of Hirayama disease. Magnetic resonance imaging (MRI) of the cervical spine was obtained both in flexion and neutra
Externí odkaz:
https://doaj.org/article/4d33421a17c94f13aff97f6a644fee78
Akademický článek
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Autor:
Akshay Rao
Publikováno v:
International Journal of Medicine and Medical Research, Vol 5, Iss 1, Pp 5-9 (2019)
Background. Brachial Monomelic Amyotrophy (BMMA) has been called as Hirayama disease (HD) when it is characterized by unilateral distal upper limb weakness and atrophy that shows progression for a limited period and is associated with typical feature
Externí odkaz:
https://doaj.org/article/659da40d8f96462fae7cf1c052f1f418
Publikováno v:
Polish Journal of Radiology. 87:584-591
Purpose: Hirayama disease (HD) is a rare disease that was commonly mis-diagnosed in the past. The importance of neutral and flexion magnetic resonance imaging (MRI) in its accurate diagnosis has been emphasized along with utility of the inter-segment
Autor:
Salvatore Iacono, Vincenzo Di Stefano, Andrea Gagliardo, Roberto Cannella, Valentina Virzì, Sonia Pagano, Antonino Lupica, Marcello Romano, Filippo Brighina
Hirayama disease (HD) is a rare, benign, and nonprogressive motor neuron disease (MND) affecting the upper limbs. It usually presents with weakness and amyotrophy in a single upper extremity with an insidious onset between adolescence and the third d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b401f6d7b94124ed37012ec2da3e8f5
http://hdl.handle.net/10447/557794
http://hdl.handle.net/10447/557794
Publikováno v:
Radiology Case Reports
Radiology Case Reports, Vol 15, Iss 9, Pp 1701-1704 (2020)
Radiology case reports, 15 (9
Radiology Case Reports, Vol 15, Iss 9, Pp 1701-1704 (2020)
Radiology case reports, 15 (9
We report the case of an 18-year old male with a history of asymmetric weakness and amyotrophy of distal upper extremities, suggestive of Hirayama disease. Magnetic resonance imaging (MRI) of the cervical spine was obtained both in flexion and neutra
Autor:
Radha Sarawagi, Sathya Narayanan, Prakash Manikka Lakshmanan, Sunitha Vellathussery Chakkalakkoombil
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 8, Pp RD03-RD04 (2014)
We report three cases of Hirayama disease, cervical flexion myelopathy presenting as unilateral or bilateral asymmetric muscular atrophy of forearm and hand involving C7 - T1 myotomes in young males. MRI revealed asymmetric cord atrophy, altered sig
Externí odkaz:
https://doaj.org/article/938680fda280470e945baacfbad6d9df
Publikováno v:
Online Journal of Health & Allied Sciences, Vol 12, Iss 3 (2013)
Hirayama disease is a monomyelic variant of motor neuron disease (MND) and has distinctive features of male predominance, asymmetric involvement of upper extremities with a self limiting course. Flexion MRI (magnetic resonance imaging) forms the main
Externí odkaz:
https://doaj.org/article/9f9423a7c49a4fb2bdbbc02e6574137b
Akademický článek
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Autor:
Fabrice Bonneville, Sorin Aldea, Pierre Brandicourt, David Brauge, José Cuesta Del Sol, Pascal Cintas
Publikováno v:
Neurochirurgie
Neurochirurgie, Elsevier Masson, 2018, 64 (4), pp.303-309. ⟨10.1016/j.neuchi.2018.04.004⟩
Neurochirurgie, Elsevier Masson, 2018, 64 (4), pp.303-309. ⟨10.1016/j.neuchi.2018.04.004⟩
Introduction. Hirayama disease is a rare cervical myelopathy predominantly affecting young adults andmainly found in Asia. It results in a pure motor distal lesion of the upper limbs with slow progression.Dynamic magnetic resonance imaging (MRI), whi