Junko Kanno - Publications

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

Journal: Endocrine journal

Published: August 12, 2026

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

Journal: Endocrine journal

Published: December 03, 2025

Long-lasting hypoglycemia through insulin degludec during acute kidney injury after diabetic ketoacidosis: A case report.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: October 14, 2025

Clinical characteristics and anti-ZSCAN1 antibody titer analysis in a nationwide survey of ROHHAD (-NET) syndrome.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 02, 2025

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

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: August 13, 2025

46,XY 17 alpha-hydroxylase/17,20 lyase deficiency with breast development: A case report and literature review.

Journal: Endocrine journal

Published: June 22, 2025

A Japanese infant with fulminant type 1 diabetes with disease-sensitive CSAD polymorphism and HLA haplotype.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: February 24, 2025

De Novo Splice Site Variant of TCF12 in a Boy With Isolated Kallmann Syndrome.

Journal: Case reports in endocrinology

Published: February 10, 2025

Seizures in pediatric thyroid storm: Two cases and a literature review.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: January 05, 2025

DHX37 variants in patients with 46,XY disorders or differences of sex development.

Journal: Human genome variation

Published: December 24, 2024

Functional Noncoding Variants in a TTTG Microsatellite on Chromosome 15q26.1 Are a Common Genetic Etiology of Congenital Hypothyroidism with Thyroid Gland in situ.

Journal: Hormone research in paediatrics

Published: December 03, 2024

Effects of enzyme replacement therapy in sibling cases of hypophosphatasia of varying severities.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: November 01, 2024