about
Interplay of LRRK2 with chaperone-mediated autophagyiPSC-derived dopamine neurons reveal differences between monozygotic twins discordant for Parkinson's diseaseLoss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficitsAmyotrophic lateral sclerosis and spinocerebellar ataxia type 2 in a family with full CAG repeat expansions of ATXN2.Multiple system atrophy and amyotrophic lateral sclerosis in a family with hexanucleotide repeat expansions in C9orf72.Wernicke's encephalopathy: an underrecognized and reversible cause of confusional state in cancer patients.Cry1 and Tef gene polymorphisms are associated with major depressive disorder in the Chinese population.Climbing fiber-Purkinje cell synaptic pathology in tremor and cerebellar degenerative diseases.Coenzyme Q10 as a Peripheral Biomarker for Multiple System AtrophyExcitatory Amino acid transporter expression in the essential tremor dentate nucleus and cerebellar cortex: A postmortem study.Macroautophagy abnormality in essential tremor.Pathological findings of anti-Yo cerebellar degeneration with Holmes tremor.The Natural History of Depression in Parkinson's Disease within 30-Month Follow-Up.Climbing fiber synaptic changes correlate with clinical features in essential tremorAge-related alterations in the metabolic profile in the hippocampus of the senescence-accelerated mouse prone 8: a spontaneous Alzheimer's disease mouse model.Glucocerebrosidase activity in Parkinson's disease with and without GBA mutationsClinical evaluation of eye movements in spinocerebellar ataxias: a prospective multicenter studyThe epigenetic regulation of HIF-1α by SIRT1 in MPP(+) treated SH-SY5Y cellsDecreased Coenzyme Q10 Levels in Multiple System Atrophy CerebellumClinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.Topiramate in treatment of tourette syndrome.Emerging therapies in Friedreich's ataxia.Cholesterol, 24-Hydroxycholesterol, and 27-Hydroxycholesterol as Surrogate Biomarkers in Cerebrospinal Fluid in Mild Cognitive Impairment and Alzheimer's Disease: A Meta-Analysis.Current concepts in the treatment of hereditary ataxias.Cerebellar Pathology in Familial vs. Sporadic Essential Tremor.Cerebellar Pathology in Early Onset and Late Onset Essential Tremor.Cerebellar pathology in childhood-onset vs. adult-onset essential tremor.Heterotopic Purkinje Cells: a Comparative Postmortem Study of Essential Tremor and Spinocerebellar Ataxias 1, 2, 3, and 6.Comparison of clinical features in pathologically confirmed PSP and MSA patients followed at a tertiary center.Cerebellar Ataxia and Hearing Impairment.Mapping Purkinje Cell Placement Along the Purkinje Cell Layer: an Analysis of Postmortem Tissue from Essential Tremor Patients vs. Controls.The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.Clinical reasoning: a 16-year-old boy with freezing of gait.Multiple system atrophy and repeat expansions in C9orf72--reply.Studying cerebellar dysfunction in neuropathy-related tremor.Teaching NeuroImage: corticospinal tract.Tardive gait.The cerebellum does more than sensory prediction error-based learning in sensorimotor adaptation tasks.Association of Tef polymorphism with depression in Parkinson disease.Resveratrol alleviates MPTP-induced motor impairments and pathological changes by autophagic degradation of α-synuclein via SIRT1-deacetylated LC3.
P50
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sheng-Han Kuo
@ast
Sheng-Han Kuo
@en
Sheng-Han Kuo
@es
Sheng-Han Kuo
@nl
Sheng-Han Kuo
@sl
type
label
Sheng-Han Kuo
@ast
Sheng-Han Kuo
@en
Sheng-Han Kuo
@es
Sheng-Han Kuo
@nl
Sheng-Han Kuo
@sl
prefLabel
Sheng-Han Kuo
@ast
Sheng-Han Kuo
@en
Sheng-Han Kuo
@es
Sheng-Han Kuo
@nl
Sheng-Han Kuo
@sl
P106
P1153
23467364400
P31
P4012
P496
0000-0002-9412-931X