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Anti-Neurofascin 155 Antibody-Positive Chronic Inflammatory Demyelinating Polyneuropathy/Combined Central and Peripheral Demyelination: Strategies for Diagnosis and Treatment Based on the Disease Mechanism

Frontiers in neurology, 2021-06, Vol.12, p.665136-665136

Kira, Jun-ichi

2021

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Serum GFAP and neurofilament light as biomarkers of disease activity and disability in NMOSD

Neurology, 2019-09, Vol.93 (13), p.e1299

2019

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Unexpected exacerbations following initiation of disease-modifying drugs in neuromyelitis optica spectrum disorder: Which factor is responsible, anti-aquaporin 4 antibodies, B cells, Th1 cells, Th2 cells, Th17 cells, or others?

Multiple sclerosis, 2017-08, Vol.23 (9), p.1300-1302

Kira, Jun-ichi

2017

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Helicobacter pylori infection and demyelinating disease of the central nervous system

Journal of neuroimmunology, 2019-04, Vol.329, p.14-19

2019

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Characteristic cerebrospinal fluid cytokine/chemokine profiles in neuromyelitis optica, relapsing remitting or primary progressive multiple sclerosis

PloS one, 2013-04, Vol.8 (4), p.e61835-e61835

2013

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Connexin 30 deficiency attenuates A2 astrocyte responses and induces severe neurodegeneration in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride Parkinson's disease animal model

Journal of neuroinflammation, 2018-08, Vol.15 (1), p.227-227, Article 227

2018

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Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy

Brain pathology (Zurich, Switzerland), 2023-05, Vol.33 (3), p.e13131-n/a

2023

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Reply to letter to the editor: Dimethyl fumarate for patients with neuromyelitis optica spectrum disorder by Pitarokoili and Gold

Multiple sclerosis, 2018-03, Vol.24 (3), p.366-367

Kira, Jun-ichi

2018

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Autoimmunity in neuromyelitis optica and opticospinal multiple sclerosis: Astrocytopathy as a common denominator in demyelinating disorders

Journal of the neurological sciences, 2011-12, Vol.311 (1), p.69-77

Kira, Jun-ichi

2011

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Clearance of peripheral nerve misfolded mutant protein by infiltrated macrophages correlates with motor neuron disease progression

Scientific reports, 2021-08, Vol.11 (1), p.16438-16438, Article 16438

2021

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A nationwide survey of combined central and peripheral demyelination in Japan

Journal of neurology, neurosurgery and psychiatry, 2016-01, Vol.87 (1), p.29-36

2016

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Atrophy of the hippocampal CA1 subfield relates to long‐term forgetting in focal epilepsy

Epilepsia (Copenhagen), 2022-10, Vol.63 (10), p.2623-2636

2022

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Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice

Human molecular genetics, 2021-05, Vol.30 (11), p.1006-1019

2021

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Insulin deficiency promotes formation of toxic amyloid-β42 conformer co-aggregating with hyper-phosphorylated tau oligomer in an Alzheimer's disease model

Neurobiology of disease, 2020-04, Vol.137, p.104739, Article 104739

2020

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A case of monozygotic twins with hereditary spastic paraplegia type 4 and epilepsy, of whom only one developed narcolepsy type 1

Journal of sleep research, 2023-11, p.e14102-e14102

2023

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Oligodendroglial connexin 47 regulates neuroinflammation upon autoimmune demyelination in a novel mouse model of multiple sclerosis

Proceedings of the National Academy of Sciences - PNAS, 2020-01, Vol.117 (4), p.2160-2169

2020

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Neuromyelitis Optica and Asian Phenotype of Multiple Sclerosis

Annals of the New York Academy of Sciences, 2008-10, Vol.1142 (1), p.58-71

Kira, Jun-ichi

2008

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ELectron microscopic abnormality and therapeutic efficacy in chronic inflammatory demyelinating polyneuropathy with anti‐neurofascin155 immunoglobulin G4 antibody

Muscle & nerve, 2018-03, Vol.57 (3), p.498-502

2018

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Early postnatal allergic airway inflammation induces dystrophic microglia leading to excitatory postsynaptic surplus and autism-like behavior

Brain, behavior, and immunity, 2021-07, Vol.95, p.362-380

2021

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HLA genotype-clinical phenotype correlations in multiple sclerosis and neuromyelitis optica spectrum disorders based on Japan MS/NMOSD Biobank data

Scientific reports, 2021-01, Vol.11 (1), p.607-16, Article 607

2021

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A Novel Autoantibody against Plexin D1 in Patients with Neuropathic Pain

Annals of neurology, 2018-08, Vol.84 (2), p.208-224

2018

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Early recurrent ischemic events after mechanical thrombectomy: effect of post-treatment intracranial hemorrhage

Journal of neurology, 2021-08, Vol.268 (8), p.2810-2820

2021

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Characterization of IgG4 anti‐neurofascin 155 antibody‐positive polyneuropathy

Annals of clinical and translational neurology, 2015-10, Vol.2 (10), p.960-971

2015

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Connexins in neuromyelitis optica: a link between astrocytopathy and demyelination

Brain (London, England : 1878), 2020-09, Vol.143 (9), p.2721-2732

2020

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Anti-Neurofascin 155 Antibody-Positive Chronic Inflammatory Demyelinating Polyneuropathy/Combined Central and Peripheral Demyelination: Strategies for Diagnosis and Treatment Based on the Disease Mechanism

Serum GFAP and neurofilament light as biomarkers of disease activity and disability in NMOSD

Unexpected exacerbations following initiation of disease-modifying drugs in neuromyelitis optica spectrum disorder: Which factor is responsible, anti-aquaporin 4 antibodies, B cells, Th1 cells, Th2 cells, Th17 cells, or others?

Helicobacter pylori infection and demyelinating disease of the central nervous system

Characteristic cerebrospinal fluid cytokine/chemokine profiles in neuromyelitis optica, relapsing remitting or primary progressive multiple sclerosis

Connexin 30 deficiency attenuates A2 astrocyte responses and induces severe neurodegeneration in a 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine hydrochloride Parkinson's disease animal model

Early and extensive alterations of glial connexins, distal oligodendrogliopathy type demyelination, and nodal/paranodal pathology are characteristic of multiple system atrophy

Reply to letter to the editor: Dimethyl fumarate for patients with neuromyelitis optica spectrum disorder by Pitarokoili and Gold

Autoimmunity in neuromyelitis optica and opticospinal multiple sclerosis: Astrocytopathy as a common denominator in demyelinating disorders

Clearance of peripheral nerve misfolded mutant protein by infiltrated macrophages correlates with motor neuron disease progression

A nationwide survey of combined central and peripheral demyelination in Japan

Atrophy of the hippocampal CA1 subfield relates to long‐term forgetting in focal epilepsy

Mutations in MME cause an autosomal-recessive Charcot-Marie-Tooth disease type 2

Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice

Insulin deficiency promotes formation of toxic amyloid-β42 conformer co-aggregating with hyper-phosphorylated tau oligomer in an Alzheimer's disease model

A case of monozygotic twins with hereditary spastic paraplegia type 4 and epilepsy, of whom only one developed narcolepsy type 1

Oligodendroglial connexin 47 regulates neuroinflammation upon autoimmune demyelination in a novel mouse model of multiple sclerosis

Neuromyelitis Optica and Asian Phenotype of Multiple Sclerosis

ELectron microscopic abnormality and therapeutic efficacy in chronic inflammatory demyelinating polyneuropathy with anti‐neurofascin155 immunoglobulin G4 antibody

Early postnatal allergic airway inflammation induces dystrophic microglia leading to excitatory postsynaptic surplus and autism-like behavior

HLA genotype-clinical phenotype correlations in multiple sclerosis and neuromyelitis optica spectrum disorders based on Japan MS/NMOSD Biobank data

A Novel Autoantibody against Plexin D1 in Patients with Neuropathic Pain

Early recurrent ischemic events after mechanical thrombectomy: effect of post-treatment intracranial hemorrhage

Characterization of IgG4 anti‐neurofascin 155 antibody‐positive polyneuropathy

Connexins in neuromyelitis optica: a link between astrocytopathy and demyelination

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