Distinguishing primary from secondary Δ4-3-oxosteroid 5β-reductase (SRD5B1, AKR1D1) deficiency by urinary steroid analysis-Reference-Cited by-同舟云学术

Distinguishing primary from secondary Δ4-3-oxosteroid 5β-reductase (SRD5B1, AKR1D1) deficiency by urinary steroid analysis

Published:2014-10-27 Issue:3 Volume:82 Page:346-351
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Yanagi Tadahiro¹,Mizuochi Tatsuki¹²,Homma Keiko³,Ueki Isao¹,Seki Yoshitaka¹,Hasegawa Tomonobu⁴,Takei Hajime⁵,Nittono Hiroshi⁵,Kurosawa Takao⁶,Matsuishi Toyojiro¹,Kimura Akihiko¹

Affiliation:

1. Department of Pediatrics and Child Health; Kurume University School of Medicine; Kurume Japan

2. Division of Gastroenterology; Hepatology and Nutrition; Cincinnati Children's Hospital Medical Center; Cincinnati OH USA

3. Central Clinical Laboratories; Keio University Hospital; Tokyo Japan

4. Department of Pediatrics; Keio University School of Medicine; Tokyo Japan

5. Institution of Bile Acid; Junshin Clinic; Tokyo Japan

6. Faculty of Pharmaceutical Sciences; Health Sciences University of Hokkaido; Hokkaido Japan

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference23 articles.

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2. Inborn errors of bile acid metabolism;Heubi;Seminars in Liver Disease,2007

3. Δ4-3-Oxosteroid 5β-reductase deficiency: failure of ursodeoxycholic acid treatment and response to chenodeoxycholic acid plus cholic acid;Clayton;Gut,1996

4. Oral cholic acid for hereditary defects of primary bile acid synthesis: a safe and effective long-term therapy;Gonzales;Gastroenterology,2009

5. Disorders of bile acid synthesis;Clayton;Journal of Inherited Metabolic Disease,2011

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