Keiko Toyooka

Toyonaka, Japan

Last Updated: 09/26/2026

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Found 14 publications

Astrocyte-vascular interactions are disturbed in cerebral white matter of adult-onset neuronal intranuclear inclusion disease.

Astrocyte-vascular interactions are disturbed in cerebral white matter of adult-onset neuronal intranuclear inclusion disease.

Journal: Journal of neuropathology and experimental neurology

Published: February 06, 2026

Familial ALS With p. L127S (L126S) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review.

Familial ALS With p. L127S (L126S) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review.

Journal: Neuropathology : official journal of the Japanese Society of Neuropathology

Published: August 08, 2025

Case report: Chronic inflammatory demyelinating polyradiculoneuropathy with severe central nervous system demyelination: a clinicopathological study.

Case report: Chronic inflammatory demyelinating polyradiculoneuropathy with severe central nervous system demyelination: a clinicopathological study.

Journal: Frontiers in immunology

Published: August 08, 2024

Linking LRP12 CGG repeat expansion to inherited peripheral neuropathy.

Linking LRP12 CGG repeat expansion to inherited peripheral neuropathy.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: January 17, 2024

Hematopoietic Prostaglandin D Synthase Is Increased in Mast Cells and Pericytes in Autopsy Myocardial Specimens from Patients with Duchenne Muscular Dystrophy.

Hematopoietic Prostaglandin D Synthase Is Increased in Mast Cells and Pericytes in Autopsy Myocardial Specimens from Patients with Duchenne Muscular Dystrophy.

Journal: International journal of molecular sciences

Published: December 28, 2023

Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.

Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.

Journal: JAMA neurology

Published: May 28, 2021

A case study of a patient with myotonic dystrophy type 1 whose gait disturbance was improved by gait training with hybrid assistive limbs

A case study of a patient with myotonic dystrophy type 1 whose gait disturbance was improved by gait training with hybrid assistive limbs

Journal: Rinsho shinkeigaku = Clinical neurology

Published: May 20, 2021

Clinical trajectory of a patient with filaminopathy who developed arrhythmogenic cardiomyopathy, myofibrillar myopathy, and multiorgan tumors.

Clinical trajectory of a patient with filaminopathy who developed arrhythmogenic cardiomyopathy, myofibrillar myopathy, and multiorgan tumors.

Journal: Neuromuscular disorders : NMD

Published: February 19, 2021

A case of systemic AL amyloidosis diagnosed on muscle biopsy

A case of systemic AL amyloidosis diagnosed on muscle biopsy

Journal: Rinsho shinkeigaku = Clinical neurology

Published: December 20, 2019

A case of meningoencephalitis associated with pembrolizumab treated for squamous cell lung cancer

A case of meningoencephalitis associated with pembrolizumab treated for squamous cell lung cancer

Journal: Rinsho shinkeigaku = Clinical neurology

Published: February 01, 2019

Microvascular disturbance with decreased pericyte coverage is prominent in the ventral horn of patients with amyotrophic lateral sclerosis.

Microvascular disturbance with decreased pericyte coverage is prominent in the ventral horn of patients with amyotrophic lateral sclerosis.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: March 06, 2015

Fabry disease.

Fabry disease.

Journal: Handbook of clinical neurology

Published: August 13, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026