Kenji Fujieda - Publications

A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression.

Journal: European journal of endocrinology

Published: November 12, 2020

A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation.

Journal: European journal of medical genetics

Published: June 26, 2020

Weight-for-height charts for Japanese children based on the year 2000 Report of School Health Statistics Research.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: January 13, 2016

High prevalence of DUOX2 mutations in Japanese patients with permanent congenital hypothyroidism or transient hypothyroidism.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: October 07, 2015

An observational study of the effectiveness and safety of growth hormone (Humatrope(®)) treatment in Japanese children with growth hormone deficiency or Turner syndrome.

Journal: Endocrine journal

Published: September 25, 2012

Development of a bioassay system for human growth hormone determination with close correlation to immunoassay.

Journal: Journal of clinical laboratory analysis

Published: September 25, 2012

Efficacy and Safety of Up to 8 Years of Long-term Growth Hormone Treatment in Short Children Born Small for Gestational Age in Japan: Analysis of the Subpopulation According to the Japanese Guideline.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: June 12, 2012

Favorable impact of growth hormone treatment on cholesterol levels in turner syndrome.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: November 02, 2011