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L

Lajos László

eotvos lorand university

H指数:30

被引数:7,419

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Voluntary exercise does not increase gastrointestinal motility but increases spatial memory, intestinal eNOS, Akt levels, and Bifidobacteria abundance in the microbiome

FRONTIERS IN PHYSIOLOGY

IF3.4

2023-08-165

OAAI

Human Induced Pluripotent Stem Cell-Derived 3D-Neurospheres Are Suitable for Neurotoxicity Screening

人诱导多能干细胞衍生的3d神经球适用于神经毒性筛选

IF5.2

2020-05-0138

OAAI

Modelling the neuropathology of lysosomal storage disorders through disease-specific human induced pluripotent stem cells

EXPERIMENTAL CELL RESEARCH

IF3.5

2019-07-0133

OAAI

Lysosomal response in relation to α-synuclein pathology differs between Parkinson's disease and multiple system atrophy

帕金森氏病与多系统萎缩之间与 α-突触核蛋白病理学相关的溶酶体反应不同

NEUROBIOLOGY OF DISEASE

IF5.6

2018-06-0115

PREAI

Neurons derived from sporadic Alzheimer's disease iPSCs reveal elevated TAU hyperphosphorylation, increased amyloid levels, and GSK3B activation

ALZHEIMERS RESEARCH & THERAPY

IF7.6

2017-12-01161

OAAI

Intracellular processing of disease-associated α-synuclein in the human brain suggests prion-like cell-to-cell spread

NEUROBIOLOGY OF DISEASE

IF5.6

2014-09-01110

PREAI

Rapidly progressive dementia with thalamic degeneration and peculiar cortical prion protein immunoreactivity, but absence of proteinase K resistant PrP: a new disease entity?

ACTA NEUROPATHOLOGICA COMMUNICATIONS

IF5.7

2013-11-1111

OA

Novel crystalloid oligodendrogliopathy in hereditary spastic paraplegia

ACTA NEUROPATHOLOGICA

IF9.3

2012-03-076

PRE

Intraneuronal Immunoreactivity for the Prion Protein Distinguishes a Subset of E200K Genetic From Sporadic Creutzfeldt-Jakob Disease

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

IF3

2012-03-0116

OAAI

A peculiar constellation of tau pathology defines a subset of dementia in the elderly

tau病理学的特殊星座定义了老年人痴呆症的子集

ACTA NEUROPATHOLOGICA

IF9.3

2011-03-2574

PRE

Genetic Creutzfeldt-Jakob disease associated with the E200K mutation: characterization of a complex proteinopathy

ACTA NEUROPATHOLOGICA

IF9.3

2010-07-0182

PRE

MAPT S305I mutation:: implications for argyrophilic grain disease

ACTA NEUROPATHOLOGICA

IF9.3

2007-12-0851

PRE

Increased incidence of genetic human prion disease in Hungary

IF8.5

2005-11-2213

PREAI

The ubiquitin-proteasome system in Creutzfeld-Jakob and Alzheimer disease:: Intracellular redistribution of components correlates with neuronal vulnerability

NEUROBIOLOGY OF DISEASE

IF5.6

2005-08-0124

PREAI

Natively unfolded tubulin polymerization promoting protein TPPP/p25 is a common marker of alpha-synucleinopathies

NEUROBIOLOGY OF DISEASE

IF5.6

2004-11-01139

PREAI

The prion protein in human neuromuscular diseases

JOURNAL OF PATHOLOGY

IF5.2

2004-10-0815

PREAI

Recognition of lumenal prion protein aggregates by post-ER quality control mechanisms is mediated by the preoctarepeat region of PrP

IF2.5

2004-03-1822

PREAI

Increased sensitivity to NMDA is involved in alcohol-withdrawal induced cytotoxicity observed in primary cultures of cortical neurones chronically pre-treated with ethanol

NEUROCHEMISTRY INTERNATIONAL

IF4

2002-06-0133

PREAI

Clinicopathological phenotype of codon 129 valine homozygote sporadic Creutzfeldt-Jakob disease

NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

IF3.4

2001-12-2542

PREAI

Prominent stress response of Purkinje cells in Creutzfeldt-Jakob disease

NEUROBIOLOGY OF DISEASE

IF5.6

2001-10-0130

PREAI