Nozomi Matsuda

A case of autosomal dominant hypophosphatemic rickets.

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

Published: August 05, 2024

Clinical management of diazoxide-unresponsive congenital hyperinsulinism: A single-center experience.

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

Published: January 09, 2024

Clinical features and treatment strategies of febrile urinary tract infection caused by extended-spectrum beta-lactamase-producing Enterobacteriaceae in children: a multicenter retrospective observational study in Japan.

Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

Published: February 01, 2022

Clinical characteristics of pediatric febrile urinary tract infection in Japan.

Journal: International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases

Published: November 21, 2020

Potential pathological role of single nucleotide polymorphism (c.787T>C) in alkaline phosphatase (ALPL) for the phenotypes of hypophosphatasia.

Journal: Endocrine journal

Published: August 12, 2020

Perinatal factors affecting growth and development at age 3 years in extremely low birth weight infants born small for gestational age.

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

Published: April 17, 2017

A case of autosomal dominant hypophosphatemic rickets.

A case of autosomal dominant hypophosphatemic rickets.

Clinical management of diazoxide-unresponsive congenital hyperinsulinism: A single-center experience.

Clinical management of diazoxide-unresponsive congenital hyperinsulinism: A single-center experience.

Clinical features and treatment strategies of febrile urinary tract infection caused by extended-spectrum beta-lactamase-producing Enterobacteriaceae in children: a multicenter retrospective observational study in Japan.

Clinical features and treatment strategies of febrile urinary tract infection caused by extended-spectrum beta-lactamase-producing Enterobacteriaceae in children: a multicenter retrospective observational study in Japan.

Clinical characteristics of pediatric febrile urinary tract infection in Japan.

Clinical characteristics of pediatric febrile urinary tract infection in Japan.

Potential pathological role of single nucleotide polymorphism (c.787T>C) in alkaline phosphatase (ALPL) for the phenotypes of hypophosphatasia.

Potential pathological role of single nucleotide polymorphism (c.787T>C) in alkaline phosphatase (ALPL) for the phenotypes of hypophosphatasia.

Colonoscopic diagnosis and reduction of recurrent intussusception owing to Henoch-Schönlein purpura without purpura.

Colonoscopic diagnosis and reduction of recurrent intussusception owing to Henoch-Schönlein purpura without purpura.

Risk of coronary artery lesions in young infants with Kawasaki disease: need for a new diagnostic method.

Risk of coronary artery lesions in young infants with Kawasaki disease: need for a new diagnostic method.

Perinatal factors affecting growth and development at age 3 years in extremely low birth weight infants born small for gestational age.

Perinatal factors affecting growth and development at age 3 years in extremely low birth weight infants born small for gestational age.

Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patients.

Lower body weight and BMI at birth were associated with early adiposity rebound in 21-hydroxylase deficiency patients.

A Case of MECP2 Duplication Syndrome with Gonadotropin-Dependent Precocious Puberty.

A Case of MECP2 Duplication Syndrome with Gonadotropin-Dependent Precocious Puberty.