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Kenji Fujieda

Hokkaido University
Asahikawa Medical College

265

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5962

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

2021 European Journal of Endocrinology
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Citations (1)
Favorable Impact of Growth Hormone Treatment on Cholesterol Levels in Turner Syndrome

2012 Clinical Pediatric Endocrinology
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Favorable Impacts of Growth Hormone (GH) Replacement Therapy on Atherogenic Risks in Japanese Children with GH Deficiency.

2012 Clinical Pediatric Endocrinology
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An observational study of the effectiveness and safety of growth hormone (Humatrope(®)) treatment in Japanese children with growth hormone deficiency or Turner syndrome.

2012 Endocrine Journal
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Citations (11)
Adult height after growth hormone treatment in Japanese children with idiopathic growth hormone deficiency: analysis from the KIGS Japan database.

2011 Journal of Pediatric Endocrinology and Metabolism
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Identification and functional analysis of novel human growth hormone–releasing hormone receptor (GHRHR) gene mutations in Japanese subjects with short stature

2011 Clinical Endocrinology
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5.78 Mb terminal deletion of chromosome 15q in a girl, evaluation of NR2F2 as candidate gene for congenital heart defects.

2011 European Journal of Medical Genetics
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Subject Index Vol. 76, 2011

2011 Hormone Research in Paediatrics
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Long-Term Efficacy and Safety of Two Doses of Growth Hormone in Short Japanese Children Born Small for Gestational Age

2011 Hormone Research in Paediatrics
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The Role of N-Terminal Pro-B-Type Natriuretic Peptide in the Diagnosis of Congestive Heart Failure in Children: Correlation With the Heart Failure Score and Comparison With B-Type Natriuretic Peptide (小児のうっ血性心不全診断におけるN-末端Pro-B型Na利尿ペプチドの役割心不全評点との相関及びB型Na利尿ペプチドとの比較)

2010 Japanese Circulation Journal-english Edition
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Citations (24)