H. Hirai

发表

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

M. Taniike, S. Nakajima, S. Okada, 1998 .

Interferon treatment on glomerulonephritis associated with hepatitis C virus

Y. Etani, Yasushi Kobayashi, S. Nakajima, 2000, Pediatric Nephrology.

Circulating levels of soluble alpha-Klotho are markedly elevated in human umbilical cord blood.

Y. Nabeshima, K. Ozono, A. Imura, 2011, The Journal of clinical endocrinology and metabolism.

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

K. Ozono, T. Kubota, N. Namba, 2011, Journal of Bone and Mineral Metabolism.

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

T. Kanzaki, K. Ozono, N. Tsugawa, 2003, Journal of Bone and Mineral Metabolism.

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

K. Ozono, T. Kubota, N. Namba, 2006, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

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

T. Nagai, S. Okada, M. Shima, 2001, Clinical and Experimental Nephrology.

The Role of Cytokines for the Pathogenesis of Hemolytic Uremic Syndrome Caused by Escherichia coli O 157:H7 Infections.

M. Monden, T. Shimazu, T. Honda, 1998 .

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

Y. Etani, S. Kurotobi, S. Kogaki, 2005, Pediatric Nephrology.

An Overgrowth Disorder Associated with Excessive Production of cGMP Due to a Gain-of-Function Mutation of the Natriuretic Peptide Receptor 2 Gene

H. Yoshikawa, K. Ozono, T. Kubota, 2012, PloS one.

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

S. Kurotobi, S. Kogaki, K. Ozono, 2006, Clinical Pediatric Endocrinology.

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

K. Ozono, T. Michigami, A. Miyauchi, 2001, Journal of Human Genetics.

Rapid deterioration of renal artery dysplasia in tuberous sclerosis.

T. Matsushita, K. Ozono, S. Nakajima, 2003, The Journal of pediatrics.

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

K. Ozono, H. Kondou, N. Namba, 2013, Hormone Research in Paediatrics.

Lack of puberty despite elevated estradiol in a 46,XY phenotypic female with Frasier syndrome.

K. Ozono, Kanako Tachikawa, T. Michigami, 2006, Endocrine journal.

Shift of Serum Osteocalcin Components between Cord Blood and Blood at Day 5 of Life

S. Nakajima, S. Okada, K. Yamaoka, 2002, Pediatric Research.

Development of hyperthyroidism in a patient with idiopathic nephrotic syndrome

T. Kubota, H. Kondou, A. Sawada, 2002, Pediatric Nephrology.

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

K. Ozono, T. Michigami, S. Nakajima, 2004, Pediatric Nephrology.

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

M. Kogo, K. Ozono, T. Kubota, 2009, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Abstracts at the 38th Kansai Calcium Conference April 26, 1997 Restaurant Palace, New Hankyu Building, Osaka, Japan

T. Fujita, Y. Fujii, S. Nakajima, 2006, Journal of Bone and Mineral Metabolism.

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

Y. Etani, S. Kogaki, K. Ozono, 2011, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.