Tetsuya Okazaki

Okayama, Japan

Last Updated: 09/26/2026

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Found 47 publications

Reply to: "When neutral isn't negative: missteps in survey data analysis".

Reply to: "When neutral isn't negative: missteps in survey data analysis".

Journal: Brain & development

Published: October 16, 2025

A Rare Case of Bartter Syndrome Type 3 Diagnosed in Elderly Age.

A Rare Case of Bartter Syndrome Type 3 Diagnosed in Elderly Age.

Journal: Case reports in endocrinology

Published: June 29, 2025

Japanese pediatric neurologist's decision regarding genetic testing for patients with developmental delay/intellectual disability: A nationwide survey.

Japanese pediatric neurologist's decision regarding genetic testing for patients with developmental delay/intellectual disability: A nationwide survey.

Journal: Brain & development

Published: February 11, 2025

Adequacy evaluation of 22-gauge needle endoscopic ultrasound-guided tissue acquisition samples and glass slides preparation for successful comprehensive genomic profiling testing: A single institute experience.

Adequacy evaluation of 22-gauge needle endoscopic ultrasound-guided tissue acquisition samples and glass slides preparation for successful comprehensive genomic profiling testing: A single institute experience.

Journal: DEN open

Published: November 14, 2024

Awareness and knowledge of pediatricians regarding genetic testing for Fragile X syndrome in Japan: A National Survey of Pediatricians Managing Developmental Delay/Intellectual disability.

Awareness and knowledge of pediatricians regarding genetic testing for Fragile X syndrome in Japan: A National Survey of Pediatricians Managing Developmental Delay/Intellectual disability.

Journal: Brain & development

Published: October 13, 2024

Genotypes and phenotypes of neurofibromatosis type 1 patients in Japan: A Hereditary Tumor Cohort Study.

Genotypes and phenotypes of neurofibromatosis type 1 patients in Japan: A Hereditary Tumor Cohort Study.

Journal: Human genome variation

Published: September 13, 2024

Weight gain achieved by frequent feeding in Floating-Harbor syndrome: A case report.

Weight gain achieved by frequent feeding in Floating-Harbor syndrome: A case report.

Journal: Pediatrics international : official journal of the Japan Pediatric Society

Published: May 01, 2024

An adolescent case of ASXL3-related disorder with delayed onset of feeding difficulty.

An adolescent case of ASXL3-related disorder with delayed onset of feeding difficulty.

Journal: BMC pediatrics

Published: July 06, 2023

Mastocytosis in a Case of Noonan Syndrome Caused by a De Novo Pathogenic CBL Variant.

Mastocytosis in a Case of Noonan Syndrome Caused by a De Novo Pathogenic CBL Variant.

Journal: Yonago acta medica

Published: June 30, 2023

Phase Lag Analysis Scalp Electroencephalography May Predict Seizure Frequencies in Patients with Childhood Epilepsy with Centrotemporal Spikes.

Phase Lag Analysis Scalp Electroencephalography May Predict Seizure Frequencies in Patients with Childhood Epilepsy with Centrotemporal Spikes.

Journal: Yonago acta medica

Published: November 17, 2022

Intractable startle epilepsy in Schuurs - Hoeijmakers syndrome.

Intractable startle epilepsy in Schuurs - Hoeijmakers syndrome.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 30, 2022

Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletion.

Clinical course of a Japanese patient with developmental delay linked to a small 6q16.1 deletion.

Journal: Human genome variation

Published: April 18, 2022

Showing 1-12 of 47

Last Updated: 09/26/2026