Results 191 to 200 of about 28,725 (268)

Clinical and Pathological Features of Vasculitic Neuropathy: A Single‐Center Study in China

open access: yesEuropean Journal of Neurology, Volume 33, Issue 3, March 2026.
Vasculitic neuropathy in mainland China predominantly presents as axonal sensorimotor neuropathy. Systemic VN shows more frequent transmural inflammatory infiltration, whereas EGPA is more common in cases without infiltration. Most treated patients achieved remission, and the overall prognosis was relatively favorable, underscoring the importance of ...
Xiaoyu Zhou   +9 more
wiley   +1 more source

Novel Biallelic PLEKHG5 Variant Associated With Intermediate Charcot‐Marie‐Tooth Disease: Case Report From South America

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background and Aims Biallelic pathogenic variants in PLEKHG5 are associated with two distinct recessive phenotypes, including distal hereditary motor neuropathy AR type 4 and intermediate Charcot‐Marie‐Tooth disease type C (CMT). No South American cases have been previously reported.
Rafael Oliveira Vidon   +5 more
wiley   +1 more source

Broadening the Clinical Spectrum of Axonal Hereditary Neuropathies: A Comparative Case Study on DNAJB2‐ and HINT1‐Related Disease

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background and Aims Differentiating hereditary axonal polyneuropathies caused by distinct gene variants remains a clinical challenge. This comparative case study of DNAJB2‐ and HINT1‐related neuropathies aimed to broaden the phenotypic spectrum associated with these genes and to explore non‐motor symptoms and quality of life (QoL) in affected ...
Bogdan Bjelica   +8 more
wiley   +1 more source

Motor Neuronopathy With Widespread Fasciculations in MCM3AP‐Related Disorder: Clinical and Muscle MRI Insights

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background Biallelic pathogenic variants in MCM3AP, encoding the germinal center–associated nuclear protein (GANP), have been linked to autosomal recessive peripheral neuropathies variably accompanied by cognitive impairment and multisystem involvement.
Ana Flávia Andrade Lemos   +4 more
wiley   +1 more source

CIDP With and Without Monoclonal Gammopathy of Undetermined Significance (MGUS): Comparison of Clinical Phenotype, Diagnostic Features, and Treatment Response

open access: yesJournal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background and Aims Monoclonal gammopathy of undetermined significance (MGUS) occurs in some patients with chronic inflammatory demyelinating polyneuropathy (CIDP), but its impact on clinical phenotype and treatment response remains unclear.
R. van Veen   +16 more
wiley   +1 more source

Fracture Detectives: A Fracture Review Match Game [PDF]

open access: yes, 2020
Hana, Gina, Sudario, Gabriel
core  

Temporal summation in human peripheral axons when stimulated transcutaneously with a 10‐kHz waveform

open access: yesExperimental Physiology, Volume 111, Issue 3, Page 1268-1278, 1 March 2026.
Abstract Transcutaneous spinal cord stimulation, as used for rehabilitation of impaired motor function after spinal cord injury, often involves a 10‐kHz waveform modulated to produce repetitive bursts of stimulation. Kilohertz‐frequency waveforms may facilitate the summation of subthreshold depolarisations, but the optimal burst duration for nerve ...
Billy L. Luu   +5 more
wiley   +1 more source

What\u27s new in orthopaedic trauma [PDF]

open access: yes, 2013
Gardner, Michael   +3 more
core   +2 more sources

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