Results 121 to 130 of about 57,018 (256)
ABSTRACT Background and Aims Chronic axonal polyneuropathy is a common disorder that often remains undiagnosed. Early detection may enhance treatment of underlying risk factors and prevent long‐term complications. The Erasmus‐Polyneuropathy symptom score (E‐PSS) is a simple and rapid screening tool, consisting of six questions (score ranges 0–14). This
Noor E. Taams +9 more
wiley +1 more source
Evaluation of serum neurofilament light chain, GFAP, and peripherin as biomarkers in hereditary transthyretin amyloidosis. [PDF]
Anan I +6 more
europepmc +1 more source
ABSTRACT Background and Aims Small fiber neuropathy (SFN) is a peripheral neuropathy causing neuropathic pain, reduced quality of life (QoL), and high societal costs. Previous studies assessed these societal costs before a definitive diagnosis was established, leaving it unclear whether diagnostic confirmation affects costs, pain intensity, or QoL ...
Dennis Kool +7 more
wiley +1 more source
Severe Axonal Polyneuropathy Revealing Eosinophilic Granulomatosis With Polyangiitis: A Case Report and Review of the Literature. [PDF]
Ait Ami S +4 more
europepmc +1 more source
ABSTRACT Background and Aim Neuropathic pain (NeuP) is widely underdiagnosed, and treatment‐related adverse events often drive nonadherence. We investigated the probable NeuP prevalence, symptoms recognition, and treatment preferences among the general population in Malaysia.
Wee‐Kiat Tan +11 more
wiley +1 more source
A Case of Advanced Charcot-Marie-Tooth Disease Showing Extreme Lumbosacral Nerve Root Hypertrophy. [PDF]
Lemchak JP +3 more
europepmc +1 more source
Neurophysiological Characteristics of Nitrous Oxide‐Induced Polyneuropathy: A Case Series
ABSTRACT Background Nitrous oxide (N2O) misuse is a growing health concern, with N2O‐induced neurological disorders increasingly reported across Europe. Among these, N2O‐induced polyneuropathy (PNP) can lead to permanent deficits, yet its neurophysiological characteristics remain inconsistently described.
Tanya Elisabeth Bentley +3 more
wiley +1 more source
Effect of Eplontersen in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy Across Genetic Variants: An Exploratory Analysis From the NEURO-TTRansform Trial. [PDF]
Gillmore JD +11 more
europepmc +1 more source
Muscle &Nerve, Volume 74, Issue 3, Page 761-762, September 2026.
Antoine Pegat +2 more
wiley +1 more source
m.10010T>C Mitochondrial Disease: A Case Report With Hypoparathyroidism and Review of the Literature
ABSTRACT Mitochondria are essential intracellular organelles that play a critical role in cellular metabolism, including the regulation of intracellular calcium signaling. Advances in genomic sequencing have facilitated the identification of rare pathogenic mitochondrial DNA (mtDNA) genetic variants in patients with unexplained endocrine disorders.
Jacob Mohr +5 more
wiley +1 more source

