about
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disordersFluorescence and autoradiographic evaluation of tau PET ligand PBB3 to α-synuclein pathology.Distinct binding of PET ligands PBB3 and AV-1451 to tau fibril strains in neurodegenerative tauopathies.Reply re: "Profile of cognitive impairment and underlying pathology in multiple system atrophy".Over-expression of map kinase phosphatase-1 (MKP-1) suppresses neuronal death through regulating JNK signaling in hypoxia/re-oxygenation.Chronic Traumatic Encephalopathy Pathology in Multiple System Atrophy.Lung cysts in Birt-Hogg-Dubé syndrome: histopathological characteristics and aberrant sequence repeats.Patterns of sensory nerve conduction abnormalities in Fisher syndrome: more predominant involvement of group Ia afferents than skin afferents.Motor axonal excitability properties are strong predictors for survival in amyotrophic lateral sclerosis.Reduced orexin immunoreactivity in Perry syndrome and multiple system atrophy.Parkinson's disease susceptibility variants and severity of Lewy body pathology.Recent advances in neuropathology, biomarkers and therapeutic approach of multiple system atrophy.Atypical multiple system atrophy is a new subtype of frontotemporal lobar degeneration: frontotemporal lobar degeneration associated with α-synuclein.Relationships between lewy and tau pathologies in 375 consecutive non-Alzheimer's olfactory bulbs.Regional analysis and genetic association of nigrostriatal degeneration in Lewy body disease.Effects of diet-induced obesity and voluntary exercise in a tauopathy mouse model: implications of persistent hyperleptinemia and enhanced astrocytic leptin receptor expression.Multiple system atrophy and apolipoprotein E.Immunohistochemical analysis of tau phosphorylation and astroglial activation with enhanced leptin receptor expression in diet-induced obesity mouse hippocampus.Pulmonary cysts of Birt-Hogg-Dubé syndrome: a clinicopathologic and immunohistochemical study of 9 families.A case of adult onset vanishing white matter disease developed after minor head traumaDifferent neurological and physiological profiles in POEMS syndrome and chronic inflammatory demyelinating polyneuropathyA patient with neuromyelitis optica with positive anti-Ro (SS-A) antibody presenting with intractable hiccup and nauseaMultifocal Conduction Blocks in Sarcoid Peripheral NeuropathyIn vivo binding of a tau imaging probe, [11 C]PBB3, in patients with progressive supranuclear palsyCorticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtypeA case of meningoencephalitis associated with macrolide-resistant Mycoplasma pneumoniae infectionTDP-43 pathology in multiple system atrophy: colocalization of TDP-43 and α-synuclein in glial cytoplasmic inclusionsα-synuclein astrogliopathy: A possible specific feature in α-synucleinopathyPET-detectable tau pathology correlates with long-term neuropsychiatric outcomes in patients with traumatic brain injuryAssociation of Tripartite Motif Containing 11 rs564309 with Tau Pathology in Progressive Supranuclear PalsyCerebrovascular pathology presenting as corticobasal syndrome: An autopsy case series of "vascular CBS"Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease"Minimal change" multiple system atrophy with limbic-predominant α-synuclein pathologyAssociation of MAPT H1 subhaplotypes with neuropathology of lewy body disease
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Shunsuke Koga
@ast
Shunsuke Koga
@en
Shunsuke Koga
@es
Shunsuke Koga
@nl
type
label
Shunsuke Koga
@ast
Shunsuke Koga
@en
Shunsuke Koga
@es
Shunsuke Koga
@nl
prefLabel
Shunsuke Koga
@ast
Shunsuke Koga
@en
Shunsuke Koga
@es
Shunsuke Koga
@nl
P106
P1153
56640722100
P31
P496
0000-0001-8868-9700