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

2023

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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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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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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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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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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 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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Clinical practice guidelines for congenital hyperinsulinism

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

2017

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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), p.1029-1037

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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Long-term outcome of ovotesticular disorder of sex development: A single center experience

International journal of urology, 2011-03, Vol.18 (3), p.231-236

2011

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

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

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

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

Vitamin B1 Deficiency Related to Excessive Soft Drink Consumption in Japan

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

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

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

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

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

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

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

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

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

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

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

Clinical practice guidelines for congenital hyperinsulinism

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

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

Long-term outcome of ovotesticular disorder of sex development: A single center experience

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