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Beta-human chorionic gonadotropin-producing neuroblastoma: an unrecognized cause of gonadotropin-independent precocious puberty

Endocrine Journal, 2022, Vol.69(3), pp.313-318

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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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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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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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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Nephrogenic diabetes insipidus caused by a novel missense variant (p.S127Y) in the AVPR2 gene

Clinical Pediatric Endocrinology, 2021, Vol.30(2), pp.115-118

2021

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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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Antibodies to Crohn’s disease peptide 353 as a diagnostic marker for pediatric Crohn’s disease: a prospective multicenter study in Japan

Journal of gastroenterology, 2020-05, Vol.55 (5), p.515-522

2020

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Utility of a rapid assay for prostaglandin E-major urinary metabolite as a biomarker in pediatric ulcerative colitis

Scientific reports, 2023-06, Vol.13 (1), p.9898-9898, Article 9898

2023

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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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Constitutional mismatch repair deficiency in childhood colorectal cancer harboring a de novo variant in the MSH6 gene: a case report

BMC gastroenterology, 2021-02, Vol.21 (1), p.60-60, Article 60

2021

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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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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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Clinical practice guidelines for the management of children with mother‐to‐child transmitted hepatitis C virus infection

Pediatrics international, 2022-01, Vol.64 (1), p.e14962-n/a

2022

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Natural history of chronic hepatitis B virus infection in children in Japan: a comparison of mother-to-child transmission with horizontal transmission

Journal of gastroenterology, 2017-09, Vol.52 (9), p.1041-1050

2017

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Thyroid hormone status in patients with severe selenium deficiency

Clinical Pediatric Endocrinology, 2018, Vol.27(2), pp.67-74

2018

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Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome

ENDOCRINE JOURNAL, 2019, Vol.66 (11), p.983-994

2019

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Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome

Clinical Pediatric Endocrinology, 2024, Vol.33(2), pp.50-58

2024

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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), p.1127-1137

2018

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Beta-human chorionic gonadotropin-producing neuroblastoma: an unrecognized cause of gonadotropin-independent precocious puberty

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

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

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

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

Nephrogenic diabetes insipidus caused by a novel missense variant (p.S127Y) in the AVPR2 gene

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

Antibodies to Crohn’s disease peptide 353 as a diagnostic marker for pediatric Crohn’s disease: a prospective multicenter study in Japan

Utility of a rapid assay for prostaglandin E-major urinary metabolite as a biomarker in pediatric ulcerative colitis

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

Constitutional mismatch repair deficiency in childhood colorectal cancer harboring a de novo variant in the MSH6 gene: a case report

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

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

Clinical practice guidelines for the management of children with mother‐to‐child transmitted hepatitis C virus infection

Natural history of chronic hepatitis B virus infection in children in Japan: a comparison of mother-to-child transmission with horizontal transmission

Thyroid hormone status in patients with severe selenium deficiency

Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome

Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome

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

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