K. Miyako

发表

Improved diabetes control by using ‘close adjustment algorithms’

T. Hara, K. Miyako, R. Kuromaru, 2004, Pediatrics international : official journal of the Japan Pediatric Society.

PD-1 gene haplotype is associated with the development of type 1 diabetes mellitus in Japanese children

K. Ihara, T. Hara, K. Miyako, 2007, Human Genetics.

The Leu544Ile polymorphism of the growth hormone receptor gene affects the serum cholesterol levels during GH treatment in children with GH deficiency

K. Ihara, N. Kinukawa, T. Hara, 2007, Clinical endocrinology.

A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency

K. Miyako, H. Kohno, Atsuko Kawano, 2014, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

PAPA-1 Is a nuclear binding partner of IGFBP-2 and modulates its growth-promoting actions.

H. Ariga, P. Cohen, J. Pintar, 2009, Molecular endocrinology.

Association study of human MTH1 gene polymorphisms with type 1 diabetes mellitus.

K. Ihara, T. Hara, N. Matsuura, 2004, Endocrine journal.

Association study between interleukin-12 receptor β1/β2 genes and type 1 diabetes or asthma in the Japanese population

K. Ihara, T. Hara, K. Kusuhara, 2003, Immunogenetics.

Clinical features of 57 patients with lipoid congenital adrenal hyperplasia: criteria for nonclassic form revisited.

S. Ida, K. Miyako, K. Kashimada, 2020, The Journal of clinical endocrinology and metabolism.

Association study of polymorphisms in SOCS family genes with type 1 diabetes mellitus

K. Ihara, T. Hara, N. Matsuura, 2006, International journal of immunogenetics.

Vitamin D deficiency rickets caused by improper lifestyle in Japanese children

K. Miyako, H. Kohno, Saori Kinjo, 2005, Pediatrics international : official journal of the Japan Pediatric Society.

Association study of the NRAMP1 gene promoter polymorphism and early-onset type 1 diabetes

K. Ihara, T. Hara, N. Matsuura, 2002, Immunogenetics.

Association study between CD30 and CD30 ligand genes and type 1 diabetes in the Japanese population

K. Ihara, T. Hara, N. Matsuura, 2002, Genes and Immunity.

H. Koga, K. Miyako, Naohiro Suga, 2010, Pediatric Cardiology.

Case Report: Adjuvant Therapy with a High Dose of Mitotane for Adrenocortical Carcinoma in a 4-year-old Boy

K. Ihara, T. Hara, M. Sanefuji, 2008, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Premature mortality and hypopituitarism

K. Miyako, R. Kuromaru, H. Kohno, 2001, The Lancet.

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

K. Nakanishi, K. Miyako, K. Nozu, 2018, Kidney international reports.

Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus

K. Miyako, Naohiro Suga, N. Takahashi, 2011, Pediatrics international : official journal of the Japan Pediatric Society.

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7

H. Okano, K. Ihara, T. Hara, 2016, Nature Genetics.

Association studies of CTLA-4, CD28, and ICOS gene polymorphisms with type 1 diabetes in the Japanese population

Nobuo Matsuura, Naoko Kinukawa, Toshiro Hara, 2001, Immunogenetics.

Hormonal regulation of IGFBP‐2 proteolysis is attenuated with progression to androgen insensitivity in the LNCaP progression model

L. Rejtõ, P. Cohen, R. Sikes, 2007, Journal of cellular physiology.