Shohei Matsuno

Kimiidera, 6418509, Japan

Last Updated: 09/26/2026

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Found 14 publications

Thyroid function, glycemic control, and diabetic nephropathy in patients with type 2 diabetes over 24 months: prospective observational study.

Thyroid function, glycemic control, and diabetic nephropathy in patients with type 2 diabetes over 24 months: prospective observational study.

Journal: BMC endocrine disorders

Published: June 05, 2022

Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional "seiza" style.

Bilateral atrophy of the extensor digitorum brevis muscle might be a useful sign for diagnosing diabetic polyneuropathy in Japanese men who do not sit in the traditional "seiza" style.

Journal: Journal of diabetes investigation

Published: May 31, 2020

Early detection of euglycemic ketoacidosis during thoracic surgery associated with empagliflozin in a patient with type 2 diabetes: A case report.

Early detection of euglycemic ketoacidosis during thoracic surgery associated with empagliflozin in a patient with type 2 diabetes: A case report.

Journal: Journal of diabetes investigation

Published: May 22, 2020

A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia.

A family in which people with a heterozygous ABCC8 gene mutation (p.Lys1385Gln) have progressed from hyperinsulinemic hypoglycemia to hyperglycemia.

Journal: Journal of diabetes

Published: July 15, 2019

Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencing.

Identification of a compound heterozygous inactivating ABCC8 gene mutation responsible for young-onset diabetes with exome sequencing.

Journal: Journal of diabetes investigation

Published: June 14, 2019

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical course.

Neonatal diabetes caused by the heterozygous Pro1198Leu mutation in the ABCC8 gene in a male infant: 6-year clinical course.

Journal: Journal of diabetes investigation

Published: May 29, 2019

Clinical polyneuropathy does not increase with prediabetes or metabolic syndrome in the Japanese general population.

Clinical polyneuropathy does not increase with prediabetes or metabolic syndrome in the Japanese general population.

Journal: Journal of diabetes investigation

Published: January 31, 2019

Identification of a variant associated with early-onset diabetes in the intron of the insulin gene with exome sequencing.

Identification of a variant associated with early-onset diabetes in the intron of the insulin gene with exome sequencing.

Journal: Journal of diabetes investigation

Published: June 11, 2018

Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody.

Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody.

Journal: Internal medicine (Tokyo, Japan)

Published: March 02, 2018

Difference in normal limit values of nerve conduction parameters between Westerners and Japanese people might need to be considered when diagnosing diabetic polyneuropathy using a Point-of-Care Sural Nerve Conduction Device (NC-stat®/DPNCheck™).

Difference in normal limit values of nerve conduction parameters between Westerners and Japanese people might need to be considered when diagnosing diabetic polyneuropathy using a Point-of-Care Sural Nerve Conduction Device (NC-stat®/DPNCheck™).

Journal: Journal of diabetes investigation

Published: September 30, 2017

Resistance to Thyroid Hormone Complicated with Type 2 Diabetes and Cardiomyopathy in a Patient with a TRβ Mutation.

Resistance to Thyroid Hormone Complicated with Type 2 Diabetes and Cardiomyopathy in a Patient with a TRβ Mutation.

Journal: Internal medicine (Tokyo, Japan)

Published: November 18, 2016

Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus.

Clinical and functional characterization of the Pro1198Leu ABCC8 gene mutation associated with permanent neonatal diabetes mellitus.

Journal: Journal of diabetes investigation

Published: October 29, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026