Gilbert Syndrome
Mostrando 1-12 de 18 artigos, teses e dissertações.
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1. Associations between Gilbert’s syndrome and personality characteristics
Abstract Objective Gilbert’s syndrome (GS) is a benign genetic disorder that is characterized by intermittent mild jaundice in which the liver doesn’t process bilirubin properly. The aim of this study was to determine whether GS patients have a different personality structure and if there are associations between properties of temperament and character
Trends Psychiatry Psychother.. Publicado em: 2021-06
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2. Host genetic and epigenetic factors in toxoplasmosis
Analysing human genetic variation provides a powerful tool in understanding risk factors for disease. Toxoplasma gondii acquired by the mother can be transmitted to the fetus. Infants with the most severe clinical signs in brain and eye are those infected early in pregnancy when fetal immunity is least well developed. Genetic analysis could provide unique in
Memórias do Instituto Oswaldo Cruz. Publicado em: 2009-03
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3. Frequency of UGT1A1*28 (Gibert´s syndrome) in patients with chronic hepatitis C virus and healthy donors / Freqüência do alelo UGT1A1*28 (síndrome de Gilbert) em pacientes portadores de hepatite crônica C e em controles sadios
Gilberts syndrome is a benign condition characterized by unconjugated hiperbilurubinemia that occurs in the absence of hemolysis or liver chronic disease. It is clinically manifested by intermittently jaundice, triggered by exposition to physical stress, low calory diet, among others. The genetic base is the reduction of the activity of UDP-glucuronosyltrans
Publicado em: 2009
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4. Population studies on Gilbert's syndrome.
Total serum bilirubin concentration was measured by an Autoanalyzer technique in 197 normal males and 102 normal females. The mean bilirubin concentration was significantly lower in the females than in the males. Total bilirubin concentration in the males showed a bimodal distribution with an antimode at 24 mumol/1 (1.4 mg/100ml). Individuals with bilirubin
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5. Unconjugated Bilirubin and an Increased Proportion of Bilirubin Monoconjugates in the Bile of Patients with Gilbert's Syndrome and Crigler-Najjar Disease
Bilirubin pigments were studied in the bile of 20 normal adults, 25 patients with Gilbert's syndrome, 9 children with Crigler-Najjar disease, and 6 patients with hemolysis, to determine how a deficiency of hepatic bilirubin UDP-glucuronosyltransferase would affect the end products of bilirubin biotransformation.
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6. Familial increased serum intestinal alkaline phosphatase: a new variant associated with Gilbert's syndrome.
Investigation of mild, inherited increased serum alkaline phosphatase activity partially combined with Gilbert's syndrome in one family showed, apart from a normal liver fraction, an intestinal isoenzyme pattern and an extra band in the agar electrophoresis. Analysis by agarose electrophoresis before and after incubation of neuraminidase showed that the extr
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7. Bone mineral densities in individuals with Gilbert’s syndrome: A cross-sectional, case-control pilot study
Pulsus Group Inc.
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8. Screening for Down's syndrome: effects, safety, and cost effectiveness of first and second trimester strategies
BMJ Group.
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9. Medical genetics: advances in brief: Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
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10. Typing of porcine reproductive and respiratory syndrome viruses by a multiplex PCR assay.
A rapid multiplex PCR assay was developed to distinguish between North American and European genotypes of porcine reproductive and respiratory syndrome (PRRS) virus after a portion of the polymerase gene (open reading frame 1b) was sequenced for two North American PRRS virus strains. DNA products with unique sizes characteristic of each genotype were obtaine
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11. Mild abnormalities in liver histology associated with chronic hepatitis: distinction from normal liver histology.
BACKGROUND: Chronic hepatitis C virus infection associated with contaminated anti-D immunoglobulin has become an issue of recent concern. The clinical course of chronic hepatitis C infection is unpredictable and histological assessment is felt to be the most reliable means of assessing disease status. Semiquantitative scoring systems have been devised, which
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12. Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.
We report the molecular characterisation of two families with Angelman syndrome referred for prenatal diagnosis, in which atypical molecular findings resulted in counselling dilemmas. The first is a familial case of Angelman syndrome in which the two affected children have mutations which affect the imprinting mechanism, as shown by the presence of paternal