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期刊名:Acta neuropathologica communications

缩写:ACTA NEUROPATHOL COM

ISSN:2051-5960

e-ISSN:2051-5960

IF/分区:6.5/Q1

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共收录本刊相关文章索引2409
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
Masami Masuda-Suzukake,Masato Hasegawa,Takashi Nonaka Masami Masuda-Suzukake
Intraneuronal α-synuclein (αS) accumulation is a central event in the pathogenesis of Parkinson's disease and dementia with Lewy bodies. The spread of αS pathology throughout the central nervous system contributes to disease progression ...
Tohgo Kanoh,Shiho Oubayashi,Kengo Furukawa et al. Tohgo Kanoh et al.
CADASIL is a hereditary cerebral small vessel disease caused by NOTCH3 mutations, leading to age-dependent vascular and neurological impairments. Despite its clinical impact, the underlying pathogenic mechanisms remain poorly understood, pa...
Víctor Giménez-Esbrí,Susanne Schwitzer,Susanne Mueller et al. Víctor Giménez-Esbrí et al.
Noise-induced hearing loss (NIHL) is a sensorineural disorder that provokes complex neuroplastic and neurodegenerative changes within the central nervous system (CNS). This study investigated the temporal dynamics of neuronal density, axona...
Arghya Bhattacharya,Hailah M Almohaimeed,Waheeb Sami Aggad et al. Arghya Bhattacharya et al.
Disease progression in Parkinson's disease has been driven by extracellular α-synuclein prion-like seeding throughout the course of the disease and therefore not just by the intracellular accumulation of the protein in isolated aggregates....
Shaoping Zhong,Yangye Lian,Binbin Zhou et al. Shaoping Zhong et al.
NOTCH2NLC-related neuronal intranuclear inclusion disease (NIID) is a progressive neurodegenerative disorder with marked clinical heterogeneity and an increasingly recognized phenotypic spectrum. Although hydrocephalus-like presentations, i...
Francesca Montarolo,Luna Berrino,Anita Maria Rominto et al. Francesca Montarolo et al.
Ataxia Telangiectasia (A-T) is a neurodegenerative disorder characterized by early onset, cerebellar ataxia and progressive motor decline. The causative gene, ATM (A-T Mutated), encodes a Ser/Thr kinase, that belongs to the phosphoinositide...
Priyanka Tripathi,Haihong Guo,Alfred Yamoah et al. Priyanka Tripathi et al.
During the progression of amyotrophic lateral sclerosis (ALS), only specific motor neurons (MNs) preferentially deteriorate, while others are spared until the disease reaches its end stage. Resilient MNs possess several protective factors, ...
Pauline Marijon,Yu Teranishi,Franck Bielle et al. Pauline Marijon et al.
Background: Spinal ependymomas (SE) account for 10% of ependymomas and are the most frequent spinal glial tumors. NF2-related Schwannomatosis (NF2-SWN) patients are predisposed to multiple SE in addition to other tumors, ...
Giuseppe Giglia,Cristian Falzone,Mariagiovanna Lorena Graceffa et al. Giuseppe Giglia et al.
Pituitary blastoma (PitB) is an exceedingly rare tumor originating from the anterior pituitary gland, first documented in 2008 in humans. It is considered pathognomonic for DICER1 syndrome, primarily affecting children, although cases in ad...