Results 121 to 130 of about 107,930 (357)

Prevalence of toxic, compression-ischemic, diabetic and atherosclerotic polyneuropathy in teleuts - primary population of Kemerovo region

open access: yesActa Biomedica Scientifica, 2013
In the study carried out in primary population of Kemerovo region - teleuts - we determined the prevalence of toxic, compression-ischemic (tunnel), diabetic and atherosclerotic polyneuropathy.
A. V. Osipov   +3 more
doaj  

Frequency of Guillain‐Barré Syndrome During the COVID‐19 Pandemic: A Multicenter Study

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Introduction/Aims The incidence of Guillain‐Barré syndrome (GBS) during the COVID‐19 pandemic varies according to country. We investigated the changes in the number of patients with GBS and their characteristics who were reported in Tokyo in 2020 at the beginning of the COVID‐19 pandemic, compared to those two years prior.
Toshiyuki Hayashi   +14 more
wiley   +1 more source

Marked efficacy of Rituximab in multifocal motor neuropathy associated with chronic lymphocytic leukemia [PDF]

open access: yes, 2016
The authors describe a patient who presented a multifocal motor neuropathy (MMN) associated with a high anti-ganglioside antibody (anti-GM1 and anti-GD1) titer at the clinical onset of a B-cell chronic lymphocytic leukemia (B-CLL). Immunomodulation (IVIg
Antonella Di, Pasquale   +6 more
core  

A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American [PDF]

open access: yes, 2018
Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) is a rare, progressive, neurodegenerative disease characterized by ataxia, spasticity and polyneuropathy.
Dougherty, Sean C.   +4 more
core   +2 more sources

Accelerometric Trunk Sensors to Detect Changes of Body Positions in Immobile Patients

open access: yesSensors, 2018
Mobilization, verticalization and position change are mandatory for severely affected neurological patients in early neurorehabilitation in order to improve neurological status and prevent complications.
Katrin Rauen   +4 more
doaj   +1 more source

Aldose reductase inhibitor ranirestat significantly improves nerve conduction velocity in diabetic polyneuropathy: A randomized double‐blind placebo‐controlled study in Japan

open access: yesJournal of Diabetes Investigation, 2018
Diabetic polyneuropathy is one of the most frequent diabetic complications, and impairs patients’ quality of life. We evaluated the efficacy and safety of ranirestat (40 mg/day) in patients with diabetic polyneuropathy.
K. Sekiguchi   +8 more
semanticscholar   +1 more source

Clinical characteristics of anti‐neurofascin 155 antibody‐positive autoimmune nodopathy in children

open access: yesPediatric Investigation, EarlyView.
Pediatric anti‐neurofascin 155 antibody autoimmune nodopathy was uncommon, featuring distal limb weakness with sensory symptoms. Cerebrospinal fluid protein levels were elevated, and neuroimaging revealed nerve root thickening. As intravenous immunoglobulin was ineffective, early immunosuppressive therapy was recommended.
Liya Cui   +13 more
wiley   +1 more source

Distal Symmetric Polyneuropathy: A Review.

open access: yesJournal of the American Medical Association (JAMA), 2015
IMPORTANCE Peripheral neuropathy is a highly prevalent and morbid condition affecting 2% to 7% of the population. Patients frequently experience pain and are at risk of falls, ulcerations, and amputations.
B. Callaghan, R. Price, E. Feldman
semanticscholar   +1 more source

Clinical perspectives and comparisons between immunoglobulin G4‐related disease and antineutrophil cytoplasmic antibody‐associated vasculitis

open access: yesRheumatology &Autoimmunity, EarlyView.
Clinical perspectives and comparisons between immunoglobulin G4‐related disease and antineutrophil cytoplasmic antibody‐associated vasculitis. Abstract Both immunoglobulin (Ig) G4‐related disease (IgG4‐RD) and antineutrophil cytoplasmic antibody (ANCA)‐associated vasculitis (AAV) are systemic disorders that affect a wide range of organs.
Wenhuan Zeng, Mingxin Bai, Yanying Liu
wiley   +1 more source

Bulbospinal muscular atrophy (Kennedy disease) responsive to immunoglobulins?

open access: yesClinical Case Reports, 2020
A 61 year old man with facial diplegia, quadruparesis, tongue atrophy/fasciculations, bulbar speech, muscle weakness/wasting, hypotonia, tremor, dysdiadochokinesia, absent tendon reflexes, fasciculations, and gynecomastia, received immunoglobulins for ...
Katharina Poustka   +3 more
doaj   +1 more source

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