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期刊名:Clinical neuropathology

缩写:CLIN NEUROPATHOL

ISSN:0722-5091

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IF/分区:0.7/Q4

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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
John Michael Newman,Jin Kyung Kim,Jeff Nirschl et al. John Michael Newman et al.
Background: Multiple system atrophy (MSA) is a progressive adult-onset synucleinopathy that remains difficult to diagnose clinically, particularly in younger patients and during early disease stages. Brainstem nuclei dege...
John Michael Newman,Jin Kyung Kim,Jeff Nirschl et al. John Michael Newman et al.
Background: Multiple system atrophy (MSA) is a progressive adult-onset synucleinopathy that remains difficult to diagnose clinically, particularly in younger patients and during early disease stages. Brainstem nuclei dege...
Tahreem Fatima,Shahzad Shams Tahreem Fatima
Objective: The medial accessory olivary nucleus (MAO), a distinct but inconsistently present subnucleus of the human inferior olivary complex, is poorly characterized despite its proposed role in cerebellar motor circuitr...
Nicola Jungbäck,Przemyslaw Grochowski,Patrick Adam et al. Nicola Jungbäck et al.
Aims: This work aims at supporting structured neuropathological assessment and early case identification for human bornavirus encephalitis. It summarizes current neuropathological and immunopathogenic findings of infectio...
Antonio Mastroianni,Sonia Greco,Concetta Castilletti Antonio Mastroianni
Background: West Nile virus (WNV) is now endemic in Europe and continues to spread to several countries, with strains 1 and 2 primarily responsible for outbreaks. According to the European Centre for Disease Prevention an...
Jeroen J de Vries,Maria João da Costa Caiado,Wilfred F A den Dunnen Jeroen J de Vries
Background: Episodic ataxias (EAs) are rare autosomal-dominant channelopathies presenting with recurrent attacks of ataxia and variable neurological features. While MRI studies suggest mild cerebellar atrophy in some pati...
Jeroen J de Vries,Maria João da Costa Caiado,Wilfred F A den Dunnen Jeroen J de Vries
This review describes the clinically and genetically heterogenous group of 52 Spinocerebellar ataxias (SCAs). After a brief description of the epidemiology and clinical spectrum, this review highlights the functional neuroanatomy, the need ...
Jennifer Garry,Sophie Sabherwal,Seamus Looby et al. Jennifer Garry et al.
Progressive multifocal leukoencephalopathy (PML) is a demyelinating central nervous system disease caused by John Cunningham virus (JCV) reactivation in immunosuppressed patients. Although classically associated with advanced HIV infection,...
Julia Schuler,Sandra Baur,Federico Fusco et al. Julia Schuler et al.
Intraoperative diagnostics in neuro-oncology face a critical gap between the morphological limitations of hematoxylin-eosin staining or toluidine blue staining and the time-intensive nature of conventional immunohistochemistry (IHC). This d...