Zobrazeno 1 - 10
of 3 506
pro vyhledávání: '"amyotrophy"'
Publikováno v:
Annales Academiae Medicae Silesiensis, Vol 78, Pp 248-252 (2024)
The Bruns-Garland syndrome (diabetic amyotrophy) is a rare disorder that affects fewer than 1% of patients with diabetes. It is manifested by unilateral or bilateral pain, weakness and muscle wasting in the proximal part of the lower limbs (proximal
Externí odkaz:
https://doaj.org/article/a60551a5841a4f8cbd5b2ad08763eb7c
Autor:
Viktoriia Iakovleva, Federico Verde, Claudia Cinnante, Alessandro Sillani, Giorgio Conte, Elena Corsini, Emilio Ciusani, Alessandra Erbetta, Vincenzo Silani, Nicola Ticozzi
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Bibrachial amyotrophy associated with an extradural CSF collection and infratentorial superficial siderosis (SS) are rare conditions that may occasionally mimic ALS. Both disorders are assumed to be due to dural tears. Case presen
Externí odkaz:
https://doaj.org/article/74a19bd1d82041adae6d240c279f62ed
Akademický článek
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Publikováno v:
Journal of Nepal Medical Association, Vol 62, Iss 279 (2024)
Hirayama disease is a rare benign neurological disease that affects the anterior horn of the spinal cord at C5 to T1, mainly at C7 and C8 due to imbalance growth between the vertebral column and the dura mater leading to microcirculatory disturbances
Externí odkaz:
https://doaj.org/article/a8ccca0e88414bb7bc54c33d2f67ca54
Publikováno v:
Clinical Case Reports, Vol 12, Iss 8, Pp n/a-n/a (2024)
Key Clinical Message Presenting a rare case of flexor carpi radialis atrophy secondary to cervical spondylotic amyotrophy. Abstract A 52‐year‐old man with a history of cervicobrachial neuralgia presented with an advanced atrophy of the right flex
Externí odkaz:
https://doaj.org/article/c21da9962a8447c39e926830f1d653e3
Publikováno v:
Indian Journal of Physical Medicine & Rehabilitation, Vol 34, Iss 1, Pp 58-62 (2024)
Hirayama illness is a rare neurological condition that first manifests as gradual muscular weakening and wasting of the distal upper limb in young males, followed within a few years by a spontaneous arrest. The spinal cord and cervical dural sac are
Externí odkaz:
https://doaj.org/article/66e34e125cdb45a0a57dc05303b0f48d
Publikováno v:
Asian Spine Journal, Vol 18, Iss 1, Pp 32-41 (2024)
Study Design Retrospective analysis of case series. Purpose This study aimed to clarify the effects of full endoscopic posterior cervical foraminotomy (FPCF) on cervical spondylotic amyotrophy (CSA). Overview of Literature The method for decompressin
Externí odkaz:
https://doaj.org/article/adf27043ec6a4aaea55ae1b386bedc94
Autor:
Veronika Vasileva, Plamen Stoev, Maya Danovska, Igor Mladenovski, Emilia Ovcharova, Emil Simeonov
Publikováno v:
Journal of IMAB, Vol 30, Iss 1, Pp 5346-5349 (2024)
Background: Neuralgic amyotrophy (NA) is a rare disorder typically characterized by an abrupt onset of upper extremity pain followed by progressive muscle weakness, atrophy and occasional sensory loss. Although NA has been hypothesized to be an autoi
Externí odkaz:
https://doaj.org/article/7159d615a56b48a585a53e8446cab778
Autor:
Krzysztof Świerz, Weronika Wacławik, Julia Szafraniec, Katarzyna Szczurek, Dawid Szczepanek, Natalia Lewoniuk, Mateusz Biesok, Julianna Szwancyber, Maksymilian Macherski, Anna Szwinge
Publikováno v:
Journal of Education, Health and Sport, Vol 63 (2024)
Neuralgic amyotrophy(NA), is a rare and highly variable neurological disorder of unknown aetiology that causes serious diagnostic problems. We described a case of NA with atrophy of the brachialis muscle in order to enrich clinicians’ knowledge abo
Externí odkaz:
https://doaj.org/article/0cc413ae91ac4a3e82d45ce644c76950
Publikováno v:
Frontiers in Surgery, Vol 11 (2024)
BackgroundCervical spondylotic amyotrophy (CSA) is a special type of cervical spondylosis based on cervical degeneration, which is mainly manifested by weakness and atrophy of upper limb muscles without obvious sensory impairment. Various diagnostic
Externí odkaz:
https://doaj.org/article/1c462da99f0a44e79654e55170be155d