Results 231 to 240 of about 1,555,906 (271)

TREATMENT OF GILBERT'S SYNDROME WITH PHENOBARBITONE

The Lancet, 1970
Abstract Thirteen patients with Gilbert's syndrome have been treated with phenobarbitone. In all instances there was a rapid fall in the plasma-bilirubin, and in three of the ten symptomatic patients the symptoms improved. The reduction in the plasma-bilirubin was associated with, and thought to be the result of, an increase in hepatic bilirubin U.D.P.
M, Black, S, Sherlock
openaire   +2 more sources

Neonatal hyperbilirubinemia and Gilbert's syndrome

Journal of Perinatal Medicine, 2002
The role of Gilbert's syndrome (GS) in neonatal hyperbilirubinemia, characterized by bilirubin levels higher than 223 microMol/L during the first seven days of life, has been investigated, evaluating the frequency of GS genotype (A(TA)7TAA polymorphism in the promoter of the gene encoding UGT1).
LAFORGIA N, FAIENZA MF, RINALDI A, D'AMATO G, RINALDI G, IOLASCON, ACHILLE   +5 more
openaire   +4 more sources

Variation in UGT1A1 activity in Gilbert's syndrome

Journal of Hepatology, 2001
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Ostrow, Jd, TIRIBELLI, CLAUDIO
openaire   +4 more sources

Gilbert's Syndrome

Vrachebnoe delo, 1979
M M, Eselev, P G, Stsepuro
openaire   +3 more sources

A Case of Acquired Gilbert’s Syndrome

Clinical Pediatrics, 2016
Leong, Jonathan, Serrano, Maria-Stella
openaire   +5 more sources

Gilbert of Gilbert's syndrome

Gastroenterology, 1998
openaire   +1 more source

Hyperbilirubinemia, Augmentation of Endothelial Function, and Decrease in Oxidative Stress in Gilbert Syndrome

Circulation, 2012
Ayumu Nakashima, Tatsuya Maruhashi, Masato Kajikawa   +2 more
exaly  

Diagnosis of Gilbert's Syndrome

Scandinavian Journal of Gastroenterology, 1981
F Hardt, E Juhl
exaly  

Haem catabolism: a novel modulator of inflammation in Gilbert's syndrome

European Journal of Clinical Investigation, 2013
Karl-Heinz Wagner, Andrew C Bulmer
exaly  

Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase () gene to phenotypes of Gilbert's syndrome and Crigler–Najjar syndrome type II

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 1998
Yukio Doida
exaly