Hirokazu Sato

发表

Association of HLA-DR, -DQ Genotype and CTLA-4 Gene Polymorphism with Graves’ Disease in Japanese Children

S. Sugihara, S. Iwama, A. Ikezaki, 2005, Hormone Research in Paediatrics.

Color Doppler ultrasonography: diagnosis of ectopic thyroid gland in patients with congenital hypothyroidism caused by thyroid dysgenesis.

N. Sasaki, Hirokazu Sato, H. Inomata, 2003, The Journal of clinical endocrinology and metabolism.

Comparison of Final Height in Monozygotic Twins, One with Idiopathic and Isolated Growth Hormone Deficiency Treated with Low Dose of Growth Hormone

S. Miyamoto, N. Sasaki, Hirokazu Sato, 2003, Hormone Research in Paediatrics.

Tachycardia-induced Cardiomyopathy in Growth Hormone Deficient Child Treated with Growth Hormone

H. Aotsuka, S. Miyamoto, Hirokazu Sato, 1996 .

Children With Irreversible Brain Damage Associated With Hypothyroidism and Multiple Intracranial Calcifications

Y. Kohno, Hirokazu Sato, J. Arii, 2002, Journal of child neurology.

Guidelines for the treatment of childhood-onset Graves’ disease in Japan, 2016

Hirokazu Sato, O. Arisaka, S. Harada, 2017, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Clinical utility of thyroid ultrasonography in the diagnosis of congenital hypothyroidism.

Hirokazu Sato, Tomoyuki Watanabe, K. Sanayama, 2002, Endocrine journal.

The Committee on Pharmaceutical Affairs, Japanese Society for Pediatric Endocrinology, and the Pediatric Thyroid Disease Committee, Japan Thyroid Association (Taskforce for the Revision of the Guidelines for the Treatment of Childhood-Onset Graves’ Disease),

Hirokazu Sato, O. Arisaka, S. Harada, 2017 .

Growth of patients with congenital hypothyroidism detected by neonatal screening in Japan

Y. Kuroda, N. Sasaki, Hirokazu Sato, 2007, Pediatrics international : official journal of the Japan Pediatric Society.

Quality of life of young adults with congenital hypothyroidism

N. Sasaki, Hirokazu Sato, N. Kakee, 2009, Pediatrics international : official journal of the Japan Pediatric Society.

Absence of Heterozygous K83E and R257X Mutations of the AIRE-1 Gene in 46 Children with Type 1 Diabetes and 44 Children with Graves’ Disease

S. Sugihara, S. Miyamoto, S. Iwama, 2005, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Comparison of methimazole and propylthiouracil in the management of children and adolescents with Graves’ disease: efficacy and adverse reactions during initial treatment and long-term outcome

Y. Kohno, S. Sugihara, N. Sasaki, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Necrosis of Femoral Capital Epiphysis (NFCE) in a Girl with Growth Hormone (GH) Deficiency Treated with Recombinant Human Growth Hormone

S. Miyamoto, N. Sasaki, Hirokazu Sato, 1994 .

Recovery Period of Hypersecretion of Thyroid‐Stimulating Hormone in Patients with Congenital Hypothyroidism Treated with Thyroid Hormone

N. Sasaki, Hirokazu Sato, H. Nakajima, 1987, Acta paediatrica Japonica : Overseas edition.

Higher dose of methimazole causes frequent adverse effects in the management of Graves’ disease in children and adolescents

Y. Kohno, S. Sugihara, N. Sasaki, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Treatment for childhood-onset Graves' disease in Japan: results of a nationwide questionnaire survey of pediatric endocrinologists and thyroidologists.

M. Mori, Toshiaki Tanaka, N. Sasaki, 2007, Thyroid : official journal of the American Thyroid Association.

EXAMINATION OF % BODY IN INFANT CASES OF ALLERGY

Hirokazu Sato, F. Iwata, M. Hara, 1996 .

Effects of bodyweight on health‐related quality of life in school‐aged children and adolescents

N. Sasaki, Hirokazu Sato, N. Nakamura, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Clinical features at diagnosis and responses to antithyroid drugs in younger children with Graves’ disease compared with adolescent patients

Y. Kohno, S. Sugihara, N. Sasaki, 2014, Journal of pediatric endocrinology & metabolism : JPEM.

Cytotoxic T lymphocyte antigen 4 gene polymorphism confers susceptibility to Type 1 diabetes in Japanese children: analysis of association with HLA genotypes and autoantibodies

S. Sugihara, S. Miyamoto, N. Sasaki, 2001, Clinical endocrinology.

Klinefelter's Syndrome with Growth Hormone Deficiency

S. Miyamoto, N. Sasaki, Hirokazu Sato, 1995 .

High prevalence of antineutrophil cytoplasmic antibody positivity in childhood onset Graves' disease treated with propylthiouracil.

M. Hattori, S. Sugihara, S. Miyamoto, 2000, The Journal of clinical endocrinology and metabolism.