Literature DB >> 4897277

Chronic nonhemolytic unconjugated hyperbilirubinemia with glucuronyl transferase deficiency. Clinical, biochemical, pharmacologic and genetic evidence for heterogeneity.

I M Arias, L M Gartner, M Cohen, J B Ezzer, A J Levi.   

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Year:  1969        PMID: 4897277     DOI: 10.1016/0002-9343(69)90224-1

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


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  57 in total

1.  Molecular biology and the diagnosis and treatment of liver diseases.

Authors:  Howard J Worman; Lin Feng; Naoto Mamiya
Journal:  World J Gastroenterol       Date:  1998-06       Impact factor: 5.742

2.  Comparison of treatments for congenital nonobstructive nonhaemolytic hyperbilirubinaemia.

Authors:  W A Arrowsmith; R B Payne; J M Littlewood
Journal:  Arch Dis Child       Date:  1975-03       Impact factor: 3.791

3.  Treatment of an atazanivir associated grade 4 hyperbilirubinaemia with efavirenz.

Authors:  O Kummer; E Mossdorf; M Battegay; L Elzi; M Bodmer; S Krähenbühl; M Haschke
Journal:  Gut       Date:  2007-10       Impact factor: 23.059

4.  Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice.

Authors:  Yoshihiro Maruo; Yoriko Morioka; Hiroshi Fujito; Sayuri Nakahara; Takahide Yanagi; Katsuyuki Matsui; Asami Mori; Hiroshi Sato; Robert H Tukey; Yoshihiro Takeuchi
Journal:  J Pediatr       Date:  2014-03-17       Impact factor: 4.406

5.  N-acetylation and debrisoquine hydroxylation polymorphisms in patients with Gilbert's syndrome.

Authors:  W Siegmund; J D Fengler; G Franke; M Zschiesche; O Eike; E Eike; P Meisel; R Wulkow
Journal:  Br J Clin Pharmacol       Date:  1991-10       Impact factor: 4.335

6.  Crigler-Najjar type II disease inheritance: a family study.

Authors:  P Labrune; A Myara; C Hennion; J P Gout; F Trivin; M Odievre
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

7.  Cosegregation of intragenic markers with a novel mutation that causes Crigler-Najjar syndrome type I: implication in carrier detection and prenatal diagnosis.

Authors:  N Moghrabi; D J Clarke; B Burchell; M Boxer
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

8.  The use of jejunal transplants to treat a genetic enzyme deficiency.

Authors:  B M Jaffe; A A Burgos; M Martinez-Noack
Journal:  Ann Surg       Date:  1996-06       Impact factor: 12.969

9.  Marked delay in indocyanine green plasma clearance with a near-normal bromosulphophthalein retention test: a constitutional abnormality?

Authors:  K Okuda; H Ohkubo; H Musha; K Kotoda; H Abe; K Tanikawa
Journal:  Gut       Date:  1976-08       Impact factor: 23.059

10.  Mapping of the mouse bilirubin UDP-glucuronosyltransferase gene (Gnt-1) to chromosome 1 by restriction fragment length variations.

Authors:  H Sato; Y Sakai; O Koiwai; T Watanabe
Journal:  Biochem Genet       Date:  1992-08       Impact factor: 1.890

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