Satoshi Kono

Hamamatsu, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 26 publications

Aceruloplasminemia with Abnormal Compound Heterozygous Mutations Developed Neurological Dysfunction during Phlebotomy Therapy.

Aceruloplasminemia with Abnormal Compound Heterozygous Mutations Developed Neurological Dysfunction during Phlebotomy Therapy.

Journal: Internal medicine (Tokyo, Japan)

Published: May 01, 2018

Neuroinflammation following disease modifying therapy in multiple sclerosis: A pilot positron emission tomography study.

Neuroinflammation following disease modifying therapy in multiple sclerosis: A pilot positron emission tomography study.

Journal: Journal of the neurological sciences

Published: October 04, 2017

The Resection of Thyroid Cancer Was Associated with the Resolution of Hyporesponsiveness to an Erythropoiesis-stimulating Agent in a Hemodialysis Patient with Aceruloplasminemia.

The Resection of Thyroid Cancer Was Associated with the Resolution of Hyporesponsiveness to an Erythropoiesis-stimulating Agent in a Hemodialysis Patient with Aceruloplasminemia.

Journal: Internal medicine (Tokyo, Japan)

Published: April 07, 2017

Extrastriatal spreading of microglial activation in Parkinson's disease: a positron emission tomography study.

Extrastriatal spreading of microglial activation in Parkinson's disease: a positron emission tomography study.

Journal: Annals of nuclear medicine

Published: April 04, 2016

Direct Comparison of Manganese Detoxification/Efflux Proteins and Molecular Characterization of ZnT10 Protein as a Manganese Transporter.

Direct Comparison of Manganese Detoxification/Efflux Proteins and Molecular Characterization of ZnT10 Protein as a Manganese Transporter.

Journal: The Journal of biological chemistry

Published: March 21, 2016

A Video Report of Brain-Lung-Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene.

A Video Report of Brain-Lung-Thyroid Syndrome in a Japanese Female With a Novel Frameshift Mutation of the NKX2-1 Gene.

Journal: Child neurology open

Published: February 26, 2016

The Possible Link between GABAergic Dysfunction and Cognitive Decline in a Patient with Idiopathic Hypoparathyroidism.

The Possible Link between GABAergic Dysfunction and Cognitive Decline in a Patient with Idiopathic Hypoparathyroidism.

Journal: Internal medicine (Tokyo, Japan)

Published: September 03, 2015

An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation.

An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation.

Journal: BBA clinical

Published: July 03, 2014

Brain and liver iron accumulation in aceruloplasminemia.

Brain and liver iron accumulation in aceruloplasminemia.

Journal: Neurology

Published: December 11, 2013

Aceruloplasminemia: an update.

Aceruloplasminemia: an update.

Journal: International review of neurobiology

Published: November 12, 2013

An autopsy case of the Marburg variant of multiple sclerosis (acute multiple sclerosis).

An autopsy case of the Marburg variant of multiple sclerosis (acute multiple sclerosis).

Journal: Internal medicine (Tokyo, Japan)

Published: August 20, 2013

GABA-A receptor impairment in cerebellar ataxia with anti-glutamic acid decarboxylase antibodies.

GABA-A receptor impairment in cerebellar ataxia with anti-glutamic acid decarboxylase antibodies.

Journal: Journal of neurology

Published: August 01, 2013

Showing 1-12 of 26

Last Updated: 09/26/2026