Kenko Azuma

Tokyo, Japan

Last Updated: 09/26/2026

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Found 20 publications

The Impact of VEGFA rs2010963 on Bilaterality and Posterior Artery Stenosis in Patients with Moyamoya Disease.

The Impact of VEGFA rs2010963 on Bilaterality and Posterior Artery Stenosis in Patients with Moyamoya Disease.

Journal: Translational stroke research

Published: January 12, 2026

Lack of Therapeutic Benefit of Ventral Intermediate Nucleus Thalamotomy for Tremor-Like Myoclonus in Two Cases of Benign Adult Familial Myoclonus Epilepsy.

Lack of Therapeutic Benefit of Ventral Intermediate Nucleus Thalamotomy for Tremor-Like Myoclonus in Two Cases of Benign Adult Familial Myoclonus Epilepsy.

Journal: Stereotactic and functional neurosurgery

Published: January 18, 2025

Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.

Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.

Journal: Journal of human genetics

Published: March 08, 2024

Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia.

Functional characterization of variants found in Japanese patients with hereditary hemorrhagic telangiectasia.

Journal: Clinical genetics

Published: November 10, 2023

The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.

The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease.

Journal: Journal of human genetics

Published: October 22, 2023

Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome.

Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome.

Journal: Scientific reports

Published: October 09, 2023

Difference in Clinical Phenotype, Mutation Position, and Structural Change of RNF213 Rare Variants Between Pediatric and Adult Japanese Patients with Moyamoya Disease.

Difference in Clinical Phenotype, Mutation Position, and Structural Change of RNF213 Rare Variants Between Pediatric and Adult Japanese Patients with Moyamoya Disease.

Journal: Translational stroke research

Published: August 30, 2023

Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis.

Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis.

Journal: Human genome variation

Published: September 12, 2022

Loss-of-function mutations in SGCE found in Japanese patients with myoclonus-dystonia.

Loss-of-function mutations in SGCE found in Japanese patients with myoclonus-dystonia.

Journal: Clinical genetics

Published: June 24, 2022

Dystonic Tremor in Adult-onset DYT-KMT2B.

Dystonic Tremor in Adult-onset DYT-KMT2B.

Journal: Internal medicine (Tokyo, Japan)

Published: January 13, 2022

Case Report: Long-Term Suppression of Paroxysmal Kinesigenic Dyskinesia After Bilateral Thalamotomy.

Case Report: Long-Term Suppression of Paroxysmal Kinesigenic Dyskinesia After Bilateral Thalamotomy.

Journal: Frontiers in neurology

Published: October 05, 2021

Predisposed genomic instability in pre-treatment bone marrow evolves to therapy-related myeloid neoplasms in malignant lymphoma.

Predisposed genomic instability in pre-treatment bone marrow evolves to therapy-related myeloid neoplasms in malignant lymphoma.

Journal: Haematologica

Published: November 09, 2019

Showing 1-12 of 20

Last Updated: 09/26/2026