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期刊名:Parkinsonism & related disorders

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ISSN:1353-8020

e-ISSN:1873-5126

IF/分区:3.4/Q2

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共收录本刊相关文章索引5414
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Anto P Rajkumar,Abdul Hye,Sue Fen Tan et al. Anto P Rajkumar et al.
Introduction: Blood-based biomarkers that can aid diagnosis of Parkinson's Disease (PD) dementia (PDD), and predict PDD onset in people with PD are urgently needed. Plasma small extracellular vesicles (SEV) reflect molecu...
Zachary Schneider,Hui Liu,Mohammad Dehestani et al. Zachary Schneider et al.
Rare damaging variants in the SLC25A46 gene were recently reported to be associated with optic atrophy and parkinsonism in compound heterozygous state. Here, we comprehensively investigated the role of SLC25A46 variation in idiopathic Parki...
Paulo Bugalho,Vítor Mendes Ferreira Paulo Bugalho
Introduction: The effects of sleep disordered breathing (SDB) in Parkinson's Disease (PD) are poorly understood. Data is uncertain regarding correlation with REM sleep behavior disorder (RBD) and the effects on non-motor ...
Praewchompoo Sathirapanya,Natlada Limotai,Narupat Suanprasert et al. Praewchompoo Sathirapanya et al.
Background: Differentiating multiple system atrophy-cerebellar subtype (MSA-C) from spinocerebellar ataxia (SCA) is often difficult due to overlapping cerebellar and autonomic manifestations. Heart rate variability (HRV) ...
Abdulmunaim M Eid,Sarah Grossen,Aaron Tanenbaum et al. Abdulmunaim M Eid et al.
Background: Parkinson's disease (PD) is clinically heterogenous. We previously identified a multi-domain classification of distinct PD subtypes in participants without dementia, yielding Motor Only, Psychiatric & Motor, a...
Vikram V Holla,Debjyoti Dhar,Riyanka Kumari et al. Vikram V Holla et al.
Pathogenic variants in TSPOAP1, encoding RIMBP1, cause ultra-rare autosomal recessive dystonia (DYT-TSPOAP1/DYT-22), with only two reports worldwide. Clinical features include upper-segment-predominant dystonia, intellectual disability, eye...
Yunli Ge,Qiya Tong,Xiaolin Song et al. Yunli Ge et al.
Background: Family caregivers of people with advanced Parkinson's disease (PD) experience substantial psychological, physical, and economic strain. The optimal intensity ("dose") of structured caregiver training to lessen...