Arika Hasegawa

Nishi, Japan

Last Updated: 09/26/2026

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Found 9 publications

FTLD-TDP-43 With Motor Neuron Disease Pathology in an Autopsied Patient With Spastic Paraplegia-30B Harbouring a Homozygous KIF1A Variant.

FTLD-TDP-43 With Motor Neuron Disease Pathology in an Autopsied Patient With Spastic Paraplegia-30B Harbouring a Homozygous KIF1A Variant.

Journal: Neuropathology and applied neurobiology

Published: December 04, 2025

Effects of Tafamidis Meglumine on Transient Focal Neurological Episodes and Meningeal Contrast Enhancement in Hereditary Transthyretin-Related Meningeal Amyloidosis: Report of Two Patients Carrying the c.265T>C (p.Y89H) Variant.

Effects of Tafamidis Meglumine on Transient Focal Neurological Episodes and Meningeal Contrast Enhancement in Hereditary Transthyretin-Related Meningeal Amyloidosis: Report of Two Patients Carrying the c.265T>C (p.Y89H) Variant.

Journal: Brain and behavior

Published: March 23, 2025

Clinical and neuropsychological features and changes to regional cerebral blood flow in ‍patients with Parkinson's disease dementia

Clinical and neuropsychological features and changes to regional cerebral blood flow in ‍patients with Parkinson's disease dementia

Journal: Rinsho shinkeigaku = Clinical neurology

Published: August 28, 2024

Blood-brain barrier dysfunction in multiple system atrophy: A human postmortem study.

Blood-brain barrier dysfunction in multiple system atrophy: A human postmortem study.

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

Published: March 18, 2024

Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder

Case of hereditary Y69H (p.Y89H) transthyretin variant leptomeningeal amyloidosis presenting with drop attacks and recurrent transient language disorder

Journal: Rinsho shinkeigaku = Clinical neurology

Published: October 01, 2023

Neuropsychological and regional cerebral blood flow of posterior parietal area features in patients with Parkinson's disease with mild cognitive impairment

Neuropsychological and regional cerebral blood flow of posterior parietal area features in patients with Parkinson's disease with mild cognitive impairment

Journal: Rinsho shinkeigaku = Clinical neurology

Published: June 26, 2022

Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.

Biallelic COX10 Mutations and PMP22 Deletion in a Family With Leigh Syndrome and Hereditary Neuropathy With Liability to Pressure Palsy.

Journal: Neurology. Genetics

Published: April 06, 2022

Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a family.

Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a family.

Journal: Journal of the neurological sciences

Published: September 01, 2016

A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: consideration of the pathology of post-polio syndrome.

A fatal neuromuscular disease in an adult patient after poliomyelitis in early childhood: consideration of the pathology of post-polio syndrome.

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

Published: June 08, 2012

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Last Updated: 09/26/2026