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The updated JSPGHAN guidelines for the management of Helicobacter pylori infection in childhood

Pediatrics international, 2020-12, Vol.62 (12), p.1315-1331

2020

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Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologists

Endocrine Journal, 2022, Vol.69(1), pp.75-83

2022

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Very young children with Prader-Willi syndrome are refractory to growth hormone-associated decreases in free thyroxine levels

Endocrine Journal, 2023, Vol.70(5), pp.501-509

2023

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Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia

American journal of medical genetics. Part A, 2016-04, Vol.170A (4), p.852-855

2016

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Vitamin B1 Deficiency Related to Excessive Soft Drink Consumption in Japan

Journal of pediatric gastroenterology and nutrition, 2018-05, Vol.66 (5), p.838-842

2018

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Dosage of hydrocortisone during late infancy is positively associated with changes in body mass index during early childhood in patients with 21-hydroxylase deficiency

Endocrine Journal, 2023, Vol.70(3), pp.333-340

2023

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Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature

Endocrine Journal, 2017, Vol.64(10), pp.947-954

2017

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Reductions in estimated glomerular filtration rate during puberty in GH-treated children born small for gestational age are associated with prematurity and low birth weight, not the dosage of GH treatment

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2023-01, Vol.32 (2), p.98-104, Article 2022-0081

2023

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Male assignment in 5α‐reductase type 2 deficiency with female external genitalia

Pediatrics international, 2021-05, Vol.63 (5), p.592-594

2021

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Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial

Biological trace element research, 2020-05, Vol.195 (1), p.71-81

2020

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Renal function in short‐statured children born small for gestational age and treated with growth hormone

Pediatrics international, 2021-07, Vol.63 (7), p.775-781

2021

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Diagnostic Pitfall: Mosaic Turner syndrome with a 46, XY lymphocyte karyotype

Pediatrics international, 2021-09, Vol.63 (9), p.1122-1123

2021

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Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis

Endocrine Journal, 2020, Vol.67(10), pp.1029-1037

2020

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Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome

Endocrine Journal, 2019, Vol.66(11), pp.983-994

2019

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Fat distribution in short‐stature children born small for gestational age

Pediatrics international, 2020-12, Vol.62 (12), p.1351-1356

2020

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Newborn screening for spinal muscular atrophy in Osaka -challenges in a Japanese pilot study

Brain & development (Tokyo. 1979), 2023-08, Vol.45 (7), p.363-371

2023

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Pediatric chronic intestinal pseudo-obstruction is a rare, serious, and intractable disease: A report of a nationwide survey in Japan

Journal of pediatric surgery, 2014-12, Vol.49 (12), p.1799-1803

2014

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Visceral adipose tissue increases shortly after the cessation of GH therapy in adults with Prader-Willi syndrome

Endocrine Journal, 2018, Vol.65(11), pp.1127-1137

2018

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Clinical practice guidelines for congenital hyperinsulinism

Clinical Pediatric Endocrinology, 2017, Vol.26(3), pp.127-152

2017

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Growth hormone treatment for extremely low birthweight children born small for gestational age

Pediatrics international, 2021-01, Vol.63 (1), p.46-52

2021

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Clinical Features, Molecular Genetics, and Long-Term Outcome in Congenital Chloride Diarrhea: A Nationwide Study in Japan

The Journal of pediatrics, 2019-11, Vol.214, p.151-157.e6

2019

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Development of an efficient one-step real-time reverse transcription polymerase chain reaction method for severe acute respiratory syndrome-coronavirus-2 detection

PloS one, 2021-06, Vol.16 (6), p.e0252789-e0252789

2021

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Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)

Clinical Pediatric Endocrinology, 2022, Vol.31(3), pp.116-143

2022

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MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene

Human genome variation, 2020, Vol.7 (1), p.4-4, Article 4

2020

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Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature

Clinical Pediatric Endocrinology, 2022, Vol.31(3), pp.144-151

2022

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The updated JSPGHAN guidelines for the management of Helicobacter pylori infection in childhood

Current status of transition medicine for 21-hydroxylase deficiency in Japan: from the perspective of pediatric endocrinologists

Very young children with Prader-Willi syndrome are refractory to growth hormone-associated decreases in free thyroxine levels

Further evidence of a mutation in CDC42 as a cause of a recognizable syndromic form of thrombocytopenia

Vitamin B1 Deficiency Related to Excessive Soft Drink Consumption in Japan

Dosage of hydrocortisone during late infancy is positively associated with changes in body mass index during early childhood in patients with 21-hydroxylase deficiency

Next generation sequencing-based mutation screening of 86 patients with idiopathic short stature

Reductions in estimated glomerular filtration rate during puberty in GH-treated children born small for gestational age are associated with prematurity and low birth weight, not the dosage of GH treatment

Male assignment in 5α‐reductase type 2 deficiency with female external genitalia

Effects of Zinc Acetate on Serum Zinc Concentrations in Chronic Liver Diseases: a Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial and a Dose Adjustment Trial

Renal function in short‐statured children born small for gestational age and treated with growth hormone

Diagnostic Pitfall: Mosaic Turner syndrome with a 46, XY lymphocyte karyotype

Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis

Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome

Fat distribution in short‐stature children born small for gestational age

Newborn screening for spinal muscular atrophy in Osaka -challenges in a Japanese pilot study

Pediatric chronic intestinal pseudo-obstruction is a rare, serious, and intractable disease: A report of a nationwide survey in Japan

Visceral adipose tissue increases shortly after the cessation of GH therapy in adults with Prader-Willi syndrome

Clinical practice guidelines for congenital hyperinsulinism

Growth hormone treatment for extremely low birthweight children born small for gestational age

Clinical Features, Molecular Genetics, and Long-Term Outcome in Congenital Chloride Diarrhea: A Nationwide Study in Japan

Development of an efficient one-step real-time reverse transcription polymerase chain reaction method for severe acute respiratory syndrome-coronavirus-2 detection

Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision)

MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene

Histological analysis of testes in patients with 5 alpha-reductase deficiency type 2: Comparison with cryptorchid testes in patients without endocrinological abnormalities and a review of the literature

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