Hiroyuki Akagawa

Tokyo, Japan

Last Updated: 09/26/2026

Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 58 publications

Biallelic loss-of-function variants in PTGIS cause recurrent cervical internal carotid artery vasospasm.

Biallelic loss-of-function variants in PTGIS cause recurrent cervical internal carotid artery vasospasm.

Journal: International journal of stroke : official journal of the International Stroke Society
Published: April 25, 2026

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

Delayed Diagnosis of Vertebrobasilar Artery Stenosis Developed During Follow-Up of Two Patients With Pediatric-Onset Moyamoya Disease.

Delayed Diagnosis of Vertebrobasilar Artery Stenosis Developed During Follow-Up of Two Patients With Pediatric-Onset Moyamoya Disease.

Journal: Cureus
Published: July 12, 2025

Association of Rare RNF213 Variants and Moyamoya Disease

Association of Rare RNF213 Variants and Moyamoya Disease

Journal: No shinkei geka. Neurological surgery
Published: May 29, 2025

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

Two novel pathogenic PDX1 variants in two Japanese patients with maturity-onset diabetes of the young.

Two novel pathogenic PDX1 variants in two Japanese patients with maturity-onset diabetes of the young.

Journal: Human genome variation
Published: December 25, 2024

Middle cerebral artery aneurysms in older women with autosomal dominant polycystic kidney disease.

Middle cerebral artery aneurysms in older women with autosomal dominant polycystic kidney disease.

Journal: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
Published: October 24, 2024

Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis.

Identification of Prostaglandin I2 Synthase Rare Variants in Patients With Williams Syndrome and Severe Peripheral Pulmonary Stenosis.

Journal: Journal of the American Heart Association
Published: April 19, 2024

Reduced histone H3K4 trimethylation in oral mucosa of patients with DYT-KMT2B.

Reduced histone H3K4 trimethylation in oral mucosa of patients with DYT-KMT2B.

Journal: Parkinsonism & related disorders
Published: April 15, 2024

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

High prevalence of copy number variations in the Japanese participants with suspected MODY.

High prevalence of copy number variations in the Japanese participants with suspected MODY.

Journal: Clinical genetics
Published: January 31, 2024

Thalamic Deep Brain Stimulation for SPG56-Related Focal Hand Dystonia.

Thalamic Deep Brain Stimulation for SPG56-Related Focal Hand Dystonia.

Journal: Journal of movement disorders
Published: January 27, 2024
Showing 1-12 of 58

Last Updated: 09/26/2026