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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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Successful induction of sclerostin in human-derived fibroblasts by 4 transcription factors and its regulation by parathyroid hormone, hypoxia, and prostaglandin E2

Bone (New York, N.Y.), 2016-04, Vol.85, p.91-98

2016

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A human skeletal overgrowth mutation increases maximal velocity and blocks desensitization of guanylyl cyclase-B

Bone (New York, N.Y.), 2013-10, Vol.56 (2), p.375-382

2013

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Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reports

American journal of medical genetics. Part A, 2016-02, Vol.170A (2), p.426-434

2016

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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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Serum Fibroblast Growth Factor 23 Is a Useful Marker to Distinguish Vitamin D-Deficient Rickets from Hypophosphatemic Rickets

Hormone research in paediatrics, 2014-01, Vol.81 (4), p.251-257

2014

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Constitutively active form of natriuretic peptide receptor 2 ameliorates experimental pulmonary arterial hypertension

Molecular therapy. Methods & clinical development, 2016-01, Vol.3 (C), p.16044-16044, Article 16044

2016

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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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Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene

American journal of medical genetics. Part A, 2014-01, Vol.164A (1), p.156-163

2014

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Clinical condition and therapy of bone diseases

Clinical calcium, 2013-12, Vol.23 (12), p.1789

2013

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Serum NT-proCNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia

Clinical endocrinology (Oxford), 2016-06, Vol.84 (6), p.845-850

2016

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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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Serum NT ‐pro CNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia

Clinical endocrinology (Oxford), 2016-06, Vol.84 (6), p.845-850

2016

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A Thermal Decomposition Process for the N2O Produced in an Adipic Acid Plant

JOURNAL OF CHEMICAL ENGINEERING OF JAPAN, 2004, Vol.37(6), pp.808-813

2004

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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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Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature

European journal of pediatrics, 2014-06, Vol.173 (6), p.799-804

2014

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Skeletal overgrowth syndrome caused by overexpression of C-type natriuretic peptide in a girl with balanced chromosomal translocation, t(1;2)(q41;q37.1)

American journal of medical genetics. Part A, 2015-05, Vol.167A (5), p.1033-1038

2015

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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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Pediatric aspects of skeletal dysplasia

Pediatric endocrinology reviews : PER, 2012-10, Vol.10 Suppl 1, p.35

2012

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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 (NPR2) gene

International journal of pediatric endocrinology, 2013-10, Vol.2013 (S1), p.O43-O43, Article O43

2013

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Laparoscopic Cholecystectomy in a 8-year-old Girl with Acalcurous Cholecystitis

Journal of the Japanese Society of Pediatric Surgeons, 1993/12/20, Vol.29(7), pp.1260-1265

1993

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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 : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2011, Vol.20 (3), p.65-71

2011

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A Japanese male patient with 'fibular aplasia, tibial campomelia and oligodactyly': an additional case report

Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2009, Vol.18 (3), p.81-86

2009

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EFFECTS OF EXERCISE INTENSITY ON RENAL CLEARANCE PARAMETERS

Japanese Journal of Physical Fitness and Sports Medicine, 1992/04/01, Vol.41(2), pp.147-155

1992

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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

Successful induction of sclerostin in human-derived fibroblasts by 4 transcription factors and its regulation by parathyroid hormone, hypoxia, and prostaglandin E2

A human skeletal overgrowth mutation increases maximal velocity and blocks desensitization of guanylyl cyclase-B

Acromesomelic dysplasia, type maroteaux caused by novel loss-of-function mutations of the NPR2 gene: Three case reports

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

Serum Fibroblast Growth Factor 23 Is a Useful Marker to Distinguish Vitamin D-Deficient Rickets from Hypophosphatemic Rickets

Constitutively active form of natriuretic peptide receptor 2 ameliorates experimental pulmonary arterial hypertension

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

Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene

Clinical condition and therapy of bone diseases

Serum NT-proCNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia

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

Serum NT ‐pro CNP levels increased after initiation of GH treatment in patients with achondroplasia/hypochondroplasia

A Thermal Decomposition Process for the N2O Produced in an Adipic Acid Plant

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

Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature

Skeletal overgrowth syndrome caused by overexpression of C-type natriuretic peptide in a girl with balanced chromosomal translocation, t(1;2)(q41;q37.1)

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

Pediatric aspects of skeletal dysplasia

An overgrowth disorder associated with excessive production of cGMP due to a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene

Laparoscopic Cholecystectomy in a 8-year-old Girl with Acalcurous Cholecystitis

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

A Japanese male patient with 'fibular aplasia, tibial campomelia and oligodactyly': an additional case report

EFFECTS OF EXERCISE INTENSITY ON RENAL CLEARANCE PARAMETERS

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