Motoharu Kawai

Yamaguchi, Japan

Last Updated: 09/26/2026

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Found 15 publications

A Japanese Patient with Hereditary Myopathy with Early Respiratory Failure Due to the p.P31732L Mutation of Titin.

A Japanese Patient with Hereditary Myopathy with Early Respiratory Failure Due to the p.P31732L Mutation of Titin.

Journal: Internal medicine (Tokyo, Japan)
Published: October 21, 2021

Chronic inflammatory demyelinating polyradiculoneuropathy with myelopathy due to massively enlarged nerve roots

Chronic inflammatory demyelinating polyradiculoneuropathy with myelopathy due to massively enlarged nerve roots

Journal: Rinsho shinkeigaku = Clinical neurology
Published: August 12, 2020

Cognitive Impairment Caused by Isolated Adrenocorticotropic Hormone Deficiency without Other Hypo-adrenalism Signs - Autoimmune Encephalopathy Mimics.

Cognitive Impairment Caused by Isolated Adrenocorticotropic Hormone Deficiency without Other Hypo-adrenalism Signs - Autoimmune Encephalopathy Mimics.

Journal: Internal medicine (Tokyo, Japan)
Published: August 02, 2019

Cytomegalovirus myositis complicated with hemophagocytic lymphohistiocytosis, acute renal failure, and colitis

Cytomegalovirus myositis complicated with hemophagocytic lymphohistiocytosis, acute renal failure, and colitis

Journal: Rinsho shinkeigaku = Clinical neurology
Published: July 03, 2018

Steroid-responsive demyelinating peripheral neuropathy associated with chronic lymphoproliferative disorders of natural killer cells.

Steroid-responsive demyelinating peripheral neuropathy associated with chronic lymphoproliferative disorders of natural killer cells.

Journal: Rinsho shinkeigaku = Clinical neurology
Published: September 29, 2017

Targeting the enhanced ER stress response in Marinesco-Sjögren syndrome.

Targeting the enhanced ER stress response in Marinesco-Sjögren syndrome.

Journal: Journal of the neurological sciences
Published: February 27, 2017

Autopsy case of the C12orf65 mutation in a patient with signs of mitochondrial dysfunction.

Autopsy case of the C12orf65 mutation in a patient with signs of mitochondrial dysfunction.

Journal: Neurology. Genetics
Published: February 06, 2017

Systemic vasculitic neuropathy diagnosed by means of (18)F-FDG PET CT

Systemic vasculitic neuropathy diagnosed by means of (18)F-FDG PET CT

Journal: Rinsho shinkeigaku = Clinical neurology
Published: January 23, 2016

Rituximab-associated progressive multifocal leukoencephalopathy derived from non-Hodgkin lymphoma: neuropathological findings and results of mefloquine treatment.

Rituximab-associated progressive multifocal leukoencephalopathy derived from non-Hodgkin lymphoma: neuropathological findings and results of mefloquine treatment.

Journal: Internal medicine (Tokyo, Japan)
Published: April 17, 2015

Leptomeningeal gliomatosis with high levels of adenosine deaminase in the cerebrospinal fluid

Leptomeningeal gliomatosis with high levels of adenosine deaminase in the cerebrospinal fluid

Journal: Rinsho shinkeigaku = Clinical neurology
Published: May 09, 2014

Sera from remitting and secondary progressive multiple sclerosis patients disrupt the blood-brain barrier.

Sera from remitting and secondary progressive multiple sclerosis patients disrupt the blood-brain barrier.

Journal: PloS one
Published: November 01, 2013

Vaccine-associated paralytic poliomyelitis showing biphasic motor paresis

Vaccine-associated paralytic poliomyelitis showing biphasic motor paresis

Journal: Rinsho shinkeigaku = Clinical neurology
Published: October 16, 2012
Showing 1-12 of 15

Last Updated: 09/26/2026