Results 1 to 10 of about 21,327 (316)

Nerve Echogenicity in Polyneuropathies of Various Etiologies—Results of a Retrospective Semi-Automatic Analysis of High-Resolution Ultrasound Images [PDF]

open access: goldDiagnostics, 2022
Echogenicity of peripheral nerves in high-resolution ultrasound (HRUS) provides insight into the structural damage of peripheral nerves in various polyneuropathies.
Anke Erdmann   +6 more
doaj   +2 more sources

Causal relationship between hypothyroidism and peripheral neuropathy: a Mendelian randomization study of European ancestry [PDF]

open access: yesFrontiers in Endocrinology
BackgroundMetabolic disorders are significant risk factors for peripheral neuropathy (PN) diseases. However, current clinical observational studies cannot fully determine the causal relationships between hypothyroidism (HT) and PN diseases.MethodsWe ...
Xiping Duan, Tianchi Zhang, Ke Wang
doaj   +2 more sources

Main metabolic and toxic polyneuropathies in clinical practice

open access: yesМедицинский совет, 2021
Polyneuropathies are diseases of the peripheral nervous system with lesions of motor, sensory or autonomic fibers which are encountered by attending physicians of almost all specialties in outpatient and clinical settings.
N. V. Pizova
doaj   +1 more source

EFFICACY OF PNEUMOMASSAGE IN THE COMPREHENSIVE TREATMENT OF POLYNEUROPATHIES OF VARIOUS ORIGINS

open access: yesВестник медицинского института «Реавиз»: Реабилитация, врач и здоровье, 2021
Objective: to evaluate the efficacy of limb pneumomassage as one of the components of comprehensive treatment for patients with polyneuropathies of various origins. Material and methods.
E. A. Dorontseva   +2 more
doaj   +1 more source

Peripheral polyneuropathy from electrodiagnostic tests: a 10-year etiology and neurophysiology overview

open access: yesArquivos de Neuro-Psiquiatria, 2021
Background: Polyneuropathies are characterized by a symmetrical impairment of the peripheral nervous system, resulting in sensory, motor and/or autonomic deficits.
Renata Dal-Prá Ducci   +6 more
doaj   +1 more source

Mixed Connective Tissue Disease with Severe Axonal Polyneuropathy: A Case Report

open access: yesOman Medical Journal, 2022
Mixed connective tissue disease (MCTD) is a unique disorder characterized by the presence of a high titer of anti-U1 ribonucloprotein antibody with overlapping features of various connective tissue disorders including systemic lupus erythematosus ...
Talal Al Lawati, Batool Hassan
doaj   +1 more source

Transcutaneous neurostimulatory treatment for peripheral polyneuropathy induced by hypereosinophilic syndrome - A case report - [PDF]

open access: yesAnesthesia and Pain Medicine, 2021
Background Hypereosinophilic syndrome is a rare disease that increases the number of circulating eosinophils in the body. It has many complications, including peripheral polyneuropathy.
Kihyug Kwon   +3 more
doaj   +1 more source

Disulfiram-induced polyneurophaty [PDF]

open access: yesVojnosanitetski Pregled, 2012
Introduction. Disulfiram is used in the treatment of chronic alcoholism, because of the unpleasant symptoms produced after ethanol intake. Although it is well tolerated in most patients, one in 15,000 patients will develop peripheral neuropathy every ...
Vujisić Slavica   +5 more
doaj   +1 more source

The impact of pain and nocturnal cramps on sleep quality in Charcot Marie Tooth disease: a case-control study [PDF]

open access: yesSleep Science, 2022
Introduction: Charcot-Marie-Tooth disease is an inherited neuropathy that presents two main forms - type 1 and type 2 -, differentiated by the speed of the nervous conduction.
Cynthia Coelho Souza   +7 more
doaj   +1 more source

Inflammatory demyelinating polyneuropathies and patient management during the COVID-19 pandemic. Literature review

open access: yesNeurologijos seminarai, 2020
Inflammatory demyelinating polyneuropathies are rare but potentially treatable disorders. They can cause a lot of difficulties in daily practice due to their clinical heterogeneity and long term immunosuppressive treatment.
R. Bunevičiūtė , A. Klimašauskienė
doaj   +1 more source

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