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Autistic children and adolescents with frequent restricted interest and repetitive behavior showed more difficulty in social cognition during mask-wearing during the COVID-19 pandemic: a multisite survey

BMC psychiatry, 2022-09, Vol.22 (1), p.608-8, Article 608

2022

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Transient Left Ventricular Contractile Dysfunction during the Treatment of Rhabdomyolysis: A Case Report and Literature Review

Internal Medicine, 2017/10/15, Vol.56(20), pp.2797-2803

2017

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Hydrochlorothiazide Effectively Reduces Urinary Calcium Excretion in Two Japanese Patients with Gain-of-Function Mutations of the Calcium-Sensing Receptor Gene

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3068-3073

2002

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Hydrochlorothiazide effectively reduces urinary calcium excretion in two Japanese patients with gain-of-function mutations of the calcium-sensing receptor gene

The journal of clinical endocrinology and metabolism, 2002-07, Vol.87 (7), p.3068-3073

2002

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Long-Term Effect of Recombinant Human Insulin-Like Growth Factor I on Metabolic and Growth Control in a Patient with Leprechaunism

The journal of clinical endocrinology and metabolism, 1998-02, Vol.83 (2), p.542-549

1998

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Gonadotropin-Releasing Hormone Analog Therapy Failed to Improve Predicted Final Height in Two Children with Central Precocious Puberty and Microcephalus

Endocrine Journal, 2000, Vol.47(SupplMarch), pp.S129-S132

2000

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Development of Central Precocious Puberty After Surgical Resection in a Boy with Craniopharyngioma: Case Report

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2000, Vol.9 (2), p.63-67

2000

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Development of Central Precocious Puberty After Surgical Resection in a Boy with Craniopharyngioma：Case Report

Clinical Pediatric Endocrinology, 2000, Vol.9 (2), p.63-67

2000

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A Boy without Growth Hormone is Growing Normally

Clinical Pediatric Endocrinology, 1996, Vol.5(1), pp.11-16

1996

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Predominance of Mutation at 1138 of the cDNA for the Fibroblast Growth Factor Receptor 3 in Japanese Patients with Achondroplasia

Clinical Pediatric Endocrinology, 1996, Vol.5(Supple8), pp.103-104

1996

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A novel mutation localized in the 3′ non-HMG box region of the SRY gene in 46, XY gonadal dysgenesis

Human molecular genetics, 1994-07, Vol.3 (7), p.1187-1189

1994

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Final Height of Patients with Idiopathic Precocious Puberty Treated with Cyproterone Acetate

Clinical Pediatric Endocrinology, 1993, Vol.2(Supple2), pp.123-126

1993

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Hyperthyroidism in Growth Hormone Deficient Children Treated with Human Growth Hormone

Clinical Pediatric Endocrinology, 1995, Vol.4(Supple6), pp.121-126

1995

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A Novel Mutation in the V2 Vasopressin Receptor Gene in Two Siblings with Nephrogenic Diabetes Insipidus

Clinical Pediatric Endocrinology, 1995, Vol.4(1), pp.33-37

1995

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A Novel Mutation in the V2 Vasopressin Receptor Gene in Two Siblings with Nephrogenic Diabetes Insipidus

Clinical Pediatric Endocrinology, 1995, Vol.4 (1), p.33-37

1995

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Experience with GH Therapy in a Patient with Osteogenesis Imperfecta

Clinical Pediatric Endocrinology, 1997, Vol.6(Supple9), pp.73-76

1997

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Clinical and Basic Aspects of Intrauterine Growth Retardation

Clinical Pediatric Endocrinology, 1997, Vol.6(Supple10), pp.115-121

1997

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Effect of Human Growth Hormone (hGH) Treatment on Growth Rate and Obesity in Prader-Willi Syndrome

Clinical Pediatric Endocrinology, 1994, Vol.3(Supple4), pp.137-143

1994

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Truncation at the C-terminus of the DAX-1 protein impairs its biological actions in patients with X-linked adrenal hypoplasia congenita

The journal of clinical endocrinology and metabolism, 1996-10, Vol.81 (10), p.3680-3685

1996

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Three Novel Mutations and a De Novo Deletion Mutation of the DAX-1 Gene in Patients with X-Linked Adrenal Hypoplasia Congenita

The journal of clinical endocrinology and metabolism, 1997-11, Vol.82 (11), p.3835-3841

1997

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Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets

Pediatric research, 2000-10, Vol.48 (4), p.536-540

2000

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Near-Normal Linear Growth in the Setting of Markedly Reduced Growth Hormone and IGF-1

Hormone research in paediatrics, 1999-04, Vol.51 (4), p.184-188

1999

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Near-normal linear growth in the setting of markedly reduced growth hormone and IGF-1. A case report

Hormone research, 1999, Vol.51 (4), p.184-188

1999

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Molecular analysis of type II 3β-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3β-hydroxysteroid dehydrogenase deficiency

Human molecular genetics, 1995-05, Vol.4 (5), p.969-971

1995

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Predominance of the mutation at 1138 of the cDNA for the fibroblast growth factor receptor 3 in Japanese patients with achondroplasia

Jinrui idengaku zasshi. Japanese journal of human genetics, 1995-12, Vol.40 (4), p.347-349

1995

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Autistic children and adolescents with frequent restricted interest and repetitive behavior showed more difficulty in social cognition during mask-wearing during the COVID-19 pandemic: a multisite survey

Transient Left Ventricular Contractile Dysfunction during the Treatment of Rhabdomyolysis: A Case Report and Literature Review

Hydrochlorothiazide Effectively Reduces Urinary Calcium Excretion in Two Japanese Patients with Gain-of-Function Mutations of the Calcium-Sensing Receptor Gene

Hydrochlorothiazide effectively reduces urinary calcium excretion in two Japanese patients with gain-of-function mutations of the calcium-sensing receptor gene

Long-Term Effect of Recombinant Human Insulin-Like Growth Factor I on Metabolic and Growth Control in a Patient with Leprechaunism

Gonadotropin-Releasing Hormone Analog Therapy Failed to Improve Predicted Final Height in Two Children with Central Precocious Puberty and Microcephalus

Development of Central Precocious Puberty After Surgical Resection in a Boy with Craniopharyngioma: Case Report

Development of Central Precocious Puberty After Surgical Resection in a Boy with Craniopharyngioma：Case Report

A Boy without Growth Hormone is Growing Normally

Predominance of Mutation at 1138 of the cDNA for the Fibroblast Growth Factor Receptor 3 in Japanese Patients with Achondroplasia

A novel mutation localized in the 3′ non-HMG box region of the SRY gene in 46, XY gonadal dysgenesis

Final Height of Patients with Idiopathic Precocious Puberty Treated with Cyproterone Acetate

Hyperthyroidism in Growth Hormone Deficient Children Treated with Human Growth Hormone

A Novel Mutation in the V2 Vasopressin Receptor Gene in Two Siblings with Nephrogenic Diabetes Insipidus

A Novel Mutation in the V2 Vasopressin Receptor Gene in Two Siblings with Nephrogenic Diabetes Insipidus

Experience with GH Therapy in a Patient with Osteogenesis Imperfecta

Clinical and Basic Aspects of Intrauterine Growth Retardation

Effect of Human Growth Hormone (hGH) Treatment on Growth Rate and Obesity in Prader-Willi Syndrome

Truncation at the C-terminus of the DAX-1 protein impairs its biological actions in patients with X-linked adrenal hypoplasia congenita

Three Novel Mutations and a De Novo Deletion Mutation of the DAX-1 Gene in Patients with X-Linked Adrenal Hypoplasia Congenita

Three novel PHEX gene mutations in Japanese patients with X-linked hypophosphatemic rickets

Near-Normal Linear Growth in the Setting of Markedly Reduced Growth Hormone and IGF-1

Near-normal linear growth in the setting of markedly reduced growth hormone and IGF-1. A case report

Molecular analysis of type II 3β-hydroxysteroid dehydrogenase gene in Japanese patients with classical 3β-hydroxysteroid dehydrogenase deficiency

Predominance of the mutation at 1138 of the cDNA for the fibroblast growth factor receptor 3 in Japanese patients with achondroplasia

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