Results 91 to 100 of about 4,299 (194)

Utilizing speech analysis to differentiate progressive supranuclear palsy from Parkinson's disease

open access: yes, 2023
Introduction: Distinguishing Parkinson\u27s disease (PD) from Progressive supranuclear palsy (PSP) at early disease stages is important for clinical trial enrollment and clinical care/prognostication. Methods: We recruited 21 participants with PSP(n = 11)
Bijan Najafi   +25 more
core   +1 more source

Exploring and Targeting the Connection of Iron and Copper Homeostasis to Neurodegenerative Diseases

open access: yesMedComm, Volume 7, Issue 6, June 2026.
Iron and copper dyshomeostasis, along with their interactions with key intrinsically disordered proteins (e.g., Aβ, tau, α‐synuclein) have a strong implication in the onset and progression of neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), Prion diseases (PrDs), Huntington's disease (HD), Wilson's disease (WD),
Xin Liu   +9 more
wiley   +1 more source

Identifying Novel Modifiable Risk Factors in Progressive Supranuclear Palsy (PSP): A Secondary Use Analysis of Clinical Trial Data

open access: yes, 2023
Much of the current research efforts to treat neurological diseases have been focused on identifying novel disease biomarkers to aid in diagnosis, provide prognostic information, and monitor disease progression.
Sharma, Mansi
core  

Utility of Far‐Field Potentials as a Biomarker of Neurodegeneration in Spinal Muscular Atrophy

open access: yesMuscle &Nerve, Volume 73, Issue 6, Page 1089-1095, June 2026.
ABSTRACT Introduction/Aims Far field potentials (FFP) have been proposed as a reliable neurophysiological prognostic biomarker in amyotrophic lateral sclerosis (ALS). This study evaluated the utility of ulnar nerve FFP as a robust research biomarker of lower motor neuron degeneration in spinal muscular atrophy (SMA).
Aicee Dawn Calma   +9 more
wiley   +1 more source

GUILLAIN-BARRÉ SYNDROME ASSOCIATED WITH ACUTE HEV HEPATITIS

open access: yesIMC Journal of Medical Science, 2008
Guillain-Barré Syndrome (GBS) otherwise known as Acute Inflammatory Polyneuritis, characterized by acute progressive limb weakness and aretlexia, is the prototype of a post infectious autoimmune disease.
Rawshan Ara Khanam   +3 more
doaj  

Cancer in SMND clinical subgroups compared to controls.

open access: yes, 2014
Odds ratios (ORs) adjusted for gender and smoking using logistic regression where case numbers were ≥5. Where cases were
Roger Pamphlett (435149)   +1 more
core   +1 more source

A case report of riboflavin transporter deficiency: A novel heterozygous pathogenic variant in the SLC52A3 gene

open access: yesMolecular Genetics and Metabolism Reports
Riboflavin transporter deficiency (RTD) is a neurodegenerative disorder that presents from infancy to adulthood with a progressive axonal neuropathy characterized by a variety of neurologic symptoms including hearing loss, weakness, bulbar palsy, and ...
Elizabeth S. Tranel   +6 more
doaj   +1 more source

Distinct UNC13A Haplotype Blocks Define Disease Severity and Survival in Chinese Amyotrophic Lateral Sclerosis

open access: yesEuropean Journal of Neurology, Volume 33, Issue 6, June 2026.
Distinct UNC13A Haplotype Blocks Define Disease Severity and Survival in Chinese Amyotrophic Lateral Sclerosis. Cailin He, Ziqin Liu, Yanchun Yuan, Linxin Tang, Meirong Wang, Yongchao Li, Qianqian Zhao, Ling Weng, Juan Du, Hanjun Wu, Fan Hu, Renshi Xu, Jifeng Guo, Lu Shen, Beisha Tang, Junling Wang*.
Cailin He   +15 more
wiley   +1 more source

Audiological findings in Brown Vialetto-Van-Laere Syndrome: A scoping review

open access: yesBrazilian Journal of Otorhinolaryngology
Objective: This study aimed to characterize audiological porfile in inviduals with Brown-Vialetto-Van Laere syndrome (BVVLS). Methods: This is a scoping review following the methodological structure developed by the Joana Briggs Institute (JBI).
Débora de Oliveira Rolim   +5 more
doaj   +1 more source

A case of neuromyelitis optica spectrum disorders, with slowly progressive bulbar palsy, mimicking a motor neuron disease

open access: yesRinsho Shinkeigaku, 2019
A 52-year old woman first noted dysphagia four months before admission followed by dysarthria two months later. She then developed weakness of all limbs and became unable to walk. All these symptoms, associated with tongue atrophy, slowly progressed, leading to the initial clinical impression of a motor neuron disease, although her nerve conduction ...
Kiyoaki, Takeda   +4 more
openaire   +3 more sources

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