Literature DB >> 9446675

UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis.

A Iolascon, M F Faienza, A Moretti, S Perrotta, E Miraglia del Giudice.   

Abstract

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Year:  1998        PMID： 9446675

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  6 in total

Review 1.  Gilbert syndrome.

Authors:  Andrew Fretzayas; Maria Moustaki; Olga Liapi; Themistocles Karpathios
Journal:  Eur J Pediatr       Date:  2011-12-09       Impact factor: 3.183

2.  Intractable neonatal jaundice due to hereditary spherocytosis and Gilbert's syndrome.

Authors:  Abdul Qader Tahir Ismail; Anjum Gandhi; Nagui El-Shimy
Journal:  BMJ Case Rep       Date:  2011-07-28

Review 3.  A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.

Authors:  Robert D Christensen; Hassan M Yaish; Patrick G Gallagher
Journal:  Pediatrics       Date:  2015-06       Impact factor: 7.124

4.  Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.

Authors:  Ann M Moyer; Jennifer M Skierka; Katrina E Kotzer; Michelle L Kluge; John L Black; Linnea M Baudhuin
Journal:  Mol Diagn Ther       Date:  2017-06       Impact factor: 4.074

5.  Jaundice with hypertrophic pyloric stenosis as an early manifestation of Gilbert syndrome.

Authors:  P Trioche; J Chalas; J Francoual; L Capel; A Lindenbaum; M Odièvre; P Labrune
Journal:  Arch Dis Child       Date:  1999-10       Impact factor: 3.791

6.  Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?

Authors:  E Beutler; T Gelbart; A Demina
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-07       Impact factor: 11.205
  6 in total

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