Relevance of urinary coproporphyrin isomers in hereditary hyperbilirubinemias-Reference-Cited by-同舟云学术

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Relevance of urinary coproporphyrin isomers in hereditary hyperbilirubinemias

Published:1989-06 Issue:3 Volume:22 Page:221-222
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Frank Margareta,Doss Manfred O.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference8 articles.

1. Alcohol and porphyrin metabolism;Doss,1985

2. Relevanz der Koproporphyrin-Isomerenbestimmung im Urin im Vergleich zur intrahepatischen (alkoholtoxischen) Cholestase;Both;Zeitschrift für Gastroenterologie,1988

3. Urinary coproporphyrin isomer distribution in Dubin-Johnson syndrome;Koskelo;Clin Chem,1967

4. Separation of the isomers I and III by thin-layer chromatography;Schermuly;Z Klin Chem Klin Bio chem,1975

5. Metabolic fate of exogenous delta-aminolevulinic acid in Dubin-Johnson syndrome;Kondo;J Lab Clin Med,1979

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Practical recommendations for biochemical and genetic diagnosis of the porphyrias;Liver International;2024-06-28

2. Rotor Syndrome Presenting as Dubin-Johnson Syndrome;Case Reports in Gastroenterology;2022-08-16

3. Dubin-Johnson Syndrome as Differential Diagnosis for Neonatal Cholestasis;Journal of Pediatric Gastroenterology & Nutrition;2021-01-28

4. Developmental changes in urinary coproporphyrin ratio in premature infants;Pediatrics International;2020-01

5. The porphyrias: fundamentals and laboratory assessment;Contemporary Practice in Clinical Chemistry;2020

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