K. Miki

发表

The sugar permeability test reflects disease activity in children and adolescents with inflammatory bowel disease.

E. Southcott, G. Davidson, R. Couper, 1998, The Journal of pediatrics.

Congenital hypothyroidism caused by a mutation in the Na+/l− symporter

N. Amino, K. Miyai, K. Tatsumi, 1997, Nature Genetics.

Prediction of non-responsiveness to standard high-dose gamma-globulin therapy in patients with acute Kawasaki disease before starting initial treatment

S. Kurotobi, T. Sano, S. Kogaki, 2006, European Journal of Pediatrics.

Pulse methylprednisolone with gammaglobulin as an initial treatment for acute Kawasaki disease

T. Sano, T. Nishigaki, K. Okada, 2009, European Journal of Pediatrics.

Hypophosphatemic Rickets Accompanying Congenital Microvillous Atrophy

Takehisa Yamamoto, M. Shima, H. Tajiri, 1998, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Effect of sho-saiko-to(xiao-chai-hu-tang) on HBeAg clearance in children with chronic hepatitis B virus infection and with sustained liver disease.

H. Tajiri, K. Miki, K. Shimuzu, 1991, The American journal of Chinese medicine.

Guidelines for the treatment of Crohn’s disease in children

T. Tomomasa, M. Konno, H. Kaneko, 2006, Pediatrics international : official journal of the Japan Pediatric Society.

Prediction of later development of thyrotoxicosis or central hypothyroidism from the cord serum thyroid-stimulating hormone level in neonates born to mothers with Graves disease.

Y. Iwatani, N. Amino, J. Tachi, 1989, The Journal of pediatrics.

Rapid and simultaneous quantification of rhamnose, mannitol, and lactulose in urine by HPLC for estimating intestinal permeability in pediatric practice.

G. Davidson, R. Butler, K. Miki, 1996, Clinical chemistry.

Recurrent T354P mutation of the Na+/I- symporter in patients with iodide transport defect.

N. Amino, K. Tatsumi, K. Miki, 1998, The Journal of clinical endocrinology and metabolism.

Mechanism for the development of ovarian cysts in patients with congenital lipoid adrenal hyperplasia.

A. Tanae, N. Katsumata, T. Tanaka,, 2000, European journal of endocrinology.

Long-term Outcome in Physical Growth, Intellectual Development and Thyroid Function of Five Patients with Transient Neonatal Thyroid Dysfunction Born to Mothers with Graves’ Disease

Y. Iwatani, N. Amino, N. Mitsuda, 1999 .

Mass Protection Program of Perinatal Hepatitis B Virus Infection in Japan and Impact of an Optional Booster Vaccination on Its Efficacy

H. Tajiri, K. Miki, S. Okada, 1991, Acta paediatrica Japonica : Overseas edition.

Case Report: Three paediatric cases of primary sclerosing cholangitis treated with ursodeoxycholic acid and sulphasalazine

Y. Etani, H. Tajiri, K. Miki, 1998, Journal of gastroenterology and hepatology.

Relationship between dose of antithyroid drugs and adverse events in pediatric patients with Graves’ disease

T. Takano, K. Ozono, N. Namba, 2017, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Congenital hypothyroidism: assessment with ultrasound.

S. Takashima, K. Miki, Y. Itoh, 1995, AJNR. American journal of neuroradiology.

Transient infantile hyperthyrotrophinaemia.

K. Miyai, H. Yabuuchi, K. Miki, 1989, Archives of disease in childhood.

Two Novel Mutations in the ED1 Gene in Japanese Families With X-Linked Hypohidrotic Ectodermal Dysplasia

Gunadi, H. Nishio, M. Matsuo, 2009, Pediatric Research.

Corrigendum: Congenital hypothyroidism caused by a mutation in the Na+/I− symporter

N. Amino, K. Miyai, K. Tatsumi, 1997, Nature Genetics.

Longitudinal Observation of a Patient with Leri-Weill Dyschondrosteosis and SHOX Haploinsufficiency

Y. Etani, K. Ozono, S. Mushiake, 2005, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Urinary sulfated bile acid concentrations in infants with biliary atresia and breast‐feeding jaundice

M. Obatake, Takanobu Moriuchi, C. Tsugawa, 2003, Pediatrics international : official journal of the Japan Pediatric Society.

A novel mutation of the down-regulated in adenoma gene in a Japanese case with congential chloride diarrhea. Mutations in brief no. 198. Online.

Y. Etani, K. Ozono, S. Mushiake, 1998, Human mutation.

A novel mutation of the down-regulated in adenoma (DRA) gene in a Japanese case with congenital chloride diarrhea

Y. Etani, K. Ozono, S. Mushiake, 1998 .

Efficacy of a multiple insulin injection regimen in teenagers with insulin-dependent diabetes. Carbohydrate and lipid oxidation measured by continuous indirect calorimetry.

M. Shichiri, H. Yabuuchi, H. Tajiri, 1987, Diabetes research and clinical practice.