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An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene

PloS one, 2012-08, Vol.7 (8), p.e42180

2012

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Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta

Journal of bone and mineral metabolism, 2011-09, Vol.29 (5), p.598-605

2011

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A Japanese Male Patient with `Fibular Aplasia, Tibial Campomelia and Oligodactyly': An Additional Case Report

Clinical Pediatric Endocrinology, 2009, Vol.18(3), pp.81-86

2009

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A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Clinical Pediatric Endocrinology, 2011, Vol.20(3), pp.65-71

2011

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Circulating Levels of Soluble α-Klotho Are Markedly Elevated in Human Umbilical Cord Blood

The journal of clinical endocrinology and metabolism, 2011-06, Vol.96 (6), p.E943-E947

2011

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Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

Endocrine Journal, 2006, Vol.53(3), pp.371-376

2006

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Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss

Clinical Pediatric Endocrinology, 2006, Vol.15(3), pp.101-107

2006

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A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Clinical Pediatric Endocrinology, 2011, Vol.20 (3), p.65-71

2011

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A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

Clinical Pediatric Endocrinology, 2006, Vol.15(1), pp.23-28

2006

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A Japanese Male Patient with ‘Fibular Aplasia, Tibial Campomelia and Oligodactyly’: An Additional Case Report

Clinical Pediatric Endocrinology, 2009, Vol.18 (3), p.81-86

2009

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Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

ENDOCRINE JOURNAL, 2006, Vol.53 (3), p.371-376

2006

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Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates

Journal of bone and mineral metabolism, 2003-01, Vol.21 (2), p.103-108

2003

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Detection and Characterization of Two Novel Mutations in the HNF4A Gene in Maturity-Onset Diabetes of the Young Type 1 in Two Japanese Families

Hormone research in paediatrics, 2013-01, Vol.79 (4), p.220-226

2013

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A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

Clinical Pediatric Endocrinology, 2006, Vol.15 (1), p.23-28

2006

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A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period

Clinical and experimental nephrology, 2001-03, Vol.5 (1), p.44-46

2001

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Examination of megalin in renal tubular epithelium from patients with Dent disease

Pediatric nephrology (Berlin, West), 2004-06, Vol.19 (6), p.612-615

2004

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P5-10-5 Klotho is expressed in placenta and its soluble form modulates canonical Wnt signaling in bone

ENDOCRINE JOURNAL, 2010, Vol.57 (suppl.2-2), p.S500-S500

2010

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Successful stenting for renal artery stenosis in a patient with Alagille syndrome

Pediatric nephrology (Berlin, West), 2005-06, Vol.20 (6), p.831-833

2005

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Isolation and characterization of the human pyruvate kinase M gene

European journal of biochemistry, 1991-05, Vol.198 (1), p.101-106

1991

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Familial hypoparathyroidism

Nihon rinshō, 2005-10, Vol.63 Suppl 10, p.330

2005

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Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 1998, Vol.7 (2), p.81-85

1998

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Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Clinical Pediatric Endocrinology, 1998, Vol.7 (2), p.81-85

1998

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Rapid deterioration of renal artery dysplasia in tuberous sclerosis

The Journal of pediatrics, 2003-09, Vol.143 (3), p.406-406

2003

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Shift of serum osteocalcin components between cord blood and blood at day 5 of life

Pediatric research, 2002-11, Vol.52 (5), p.656-659

2002

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A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

Journal of human genetics, 2001-01, Vol.46 (1), p.41-44

2001

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An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 gene

Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta

A Japanese Male Patient with `Fibular Aplasia, Tibial Campomelia and Oligodactyly': An Additional Case Report

A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

Circulating Levels of Soluble α-Klotho Are Markedly Elevated in Human Umbilical Cord Blood

Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

Beneficial Effect of Oral Bisphosphonate Treatment on Bone Loss Induced by Chronic Administration of Furosemide without Alteration of Its Administration and Urinary Calcium Loss

A Male Patient with Humoral Hypercalcemia of Malignancy (HHM) with Leukocytosis Caused by Cutaneous Squamous Cell Carcinoma Resulting from Recessive Dystrophic Epidermolysis Bullosa

A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

A Japanese Male Patient with ‘Fibular Aplasia, Tibial Campomelia and Oligodactyly’: An Additional Case Report

Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome

Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates

Detection and Characterization of Two Novel Mutations in the HNF4A Gene in Maturity-Onset Diabetes of the Young Type 1 in Two Japanese Families

A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency

A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period

Examination of megalin in renal tubular epithelium from patients with Dent disease

P5-10-5 Klotho is expressed in placenta and its soluble form modulates canonical Wnt signaling in bone

Successful stenting for renal artery stenosis in a patient with Alagille syndrome

Isolation and characterization of the human pyruvate kinase M gene

Familial hypoparathyroidism

Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Treatment with Cytochrome c and Evaluation of Insulin Secretion in a Patient with Kearns-Sayre Syndrome

Rapid deterioration of renal artery dysplasia in tuberous sclerosis

Shift of serum osteocalcin components between cord blood and blood at day 5 of life

A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

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