Hirohito Shima

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

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

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

Trends in endogenous insulin secretion capacity and anti-islet autoantibody titers in two childhood-onset slowly progressive insulin-dependent diabetes mellitus cases.

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

Published: May 23, 2024

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

Trends in endogenous insulin secretion capacity and anti-islet autoantibody titers in two childhood-onset slowly progressive insulin-dependent diabetes mellitus cases.

Trends in endogenous insulin secretion capacity and anti-islet autoantibody titers in two childhood-onset slowly progressive insulin-dependent diabetes mellitus cases.

A case of 49,XXXYY followed-up from infancy to adulthood with review of literature.

A case of 49,XXXYY followed-up from infancy to adulthood with review of literature.

Marked hypercalcemia due to maxacalcitol ointment use in a patient with severe motor and intellectual disabilities.

Marked hypercalcemia due to maxacalcitol ointment use in a patient with severe motor and intellectual disabilities.

Solitary median maxillary central incisor syndrome caused by 22q11.2 microdeletion.

Solitary median maxillary central incisor syndrome caused by 22q11.2 microdeletion.