Kenichi Kashimada

Tokyo, 1578535, Japan

Last Updated: 09/26/2026

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Found 118 publications

Clinical features of hereditary adrenocortical unresponsiveness to adrenocorticotropin (HAUA) in Japan: from a nationwide questionnaire based survey.

Clinical features of hereditary adrenocortical unresponsiveness to adrenocorticotropin (HAUA) in Japan: from a nationwide questionnaire based survey.

Journal: Endocrine journal

Published: August 12, 2026

Gonadotropin Suppression During Mini-Puberty as an Early Biomarker of Classic 21-Hydroxylase Deficiency.

Gonadotropin Suppression During Mini-Puberty as an Early Biomarker of Classic 21-Hydroxylase Deficiency.

Journal: Endocrinology, diabetes & metabolism

Published: June 27, 2026

Once-weekly somapacitan enhances linear growth in girls with Turner syndrome: a randomized controlled phase 3 study.

Once-weekly somapacitan enhances linear growth in girls with Turner syndrome: a randomized controlled phase 3 study.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 09, 2026

GATA4 Single-Amino Acid Deletion in a Male Patient With Congenital Heart Defects, Differences of Sex Development, and Diaphragmatic Hernia.

GATA4 Single-Amino Acid Deletion in a Male Patient With Congenital Heart Defects, Differences of Sex Development, and Diaphragmatic Hernia.

Journal: Clinical genetics

Published: April 24, 2026

Congenital aldosterone deficiency and its resistance.

Congenital aldosterone deficiency and its resistance.

Journal: Endocrine journal

Published: March 29, 2026

Whole-genome discovery of pathogenic snRNA variants and efficient extended-exome screening.

Whole-genome discovery of pathogenic snRNA variants and efficient extended-exome screening.

Journal: iScience

Published: March 02, 2026

Repeated and Severe Salt-Wasting Crisis in a Case of Type 1 Pseudohypoaldosteronism.

Repeated and Severe Salt-Wasting Crisis in a Case of Type 1 Pseudohypoaldosteronism.

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

Published: February 10, 2026

Health-Related Quality of Life and Its Related Factors in Adolescents and Adults With Prader-Willi Syndrome in Japan.

Health-Related Quality of Life and Its Related Factors in Adolescents and Adults With Prader-Willi Syndrome in Japan.

Journal: American journal of medical genetics. Part A

Published: January 06, 2026

Clinical practice guidelines for the management of differences of sex development in Japan.

Clinical practice guidelines for the management of differences of sex development in Japan.

Journal: Endocrine journal

Published: December 03, 2025

Long-Term Efficacy and Safety of Glycerol Phenylbutyrate in Japanese Patients With Urea Cycle Disorders: Results From a Phase 3 Switch-Over and 12-Month Extension Study.

Long-Term Efficacy and Safety of Glycerol Phenylbutyrate in Japanese Patients With Urea Cycle Disorders: Results From a Phase 3 Switch-Over and 12-Month Extension Study.

Journal: JIMD reports

Published: December 01, 2025

Congenital adrenal hypoplasia with neurodevelopmental delay due to contiguous Xp21 deletion: a case series with review of literature.

Congenital adrenal hypoplasia with neurodevelopmental delay due to contiguous Xp21 deletion: a case series with review of literature.

Journal: Endocrine journal

Published: November 24, 2025

A Two-Step LC-MS/MS method to differentiate 21OHD and PORD in Screen-Positive newborns.

A Two-Step LC-MS/MS method to differentiate 21OHD and PORD in Screen-Positive newborns.

Journal: Endocrine

Published: November 14, 2025

Showing 1-12 of 118

Last Updated: 09/26/2026