Works matching DE "HEREDITARY hyperbilirubinemia"
Results: 16
Inherited Unconjugated Hyperbilirubinemias and Radical Cancer Surgery: Perioperative Concerns for Bilateral Modified Radical Mastectomy.
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- Archives of Anesthesiology & Critical Care, 2022, v. 8, n. 4, p. 336
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- Article
Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.
- Published in:
- 2015
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- Publication type:
- Case Study
The Prevalence of Abnormal Cerebro-Placental Doppler Indices Ratio [CPR] in Hypertensive Disorders of Pregnancy.
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- Journal of the Medical Association of Thailand, 2018, v. 101, n. 8, p. 1025
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- Article
Diagnostic criteria and contributors to Gilbert’s syndrome.
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- Critical Reviews in Clinical Laboratory Sciences, 2018, v. 55, n. 2, p. 129, doi. 10.1080/10408363.2018.1428526
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- Article
Radionuclide cholescintigraphy in genetically confirmed Rotor syndrome.
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- Pediatrics International, 2015, v. 57, n. 5, p. 981, doi. 10.1111/ped.12676
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- Article
Perioperative management of a patient with Gilberts syndrome and rheumatic heart disease.
- Published in:
- 2012
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- Publication type:
- Case Study
The first Turkish family with Rotor syndrome diagnosed at the molecular level.
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- Türk Pediatri Arşivi, 2020, v. 55, n. 4, p. 430, doi. 10.14744/TurkPediatriArs.2019.55798
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- Article
GENOTYPE-PHENOTYPE CORRELATION IN TUNISIAN RETT SYNDROME PATIENTS.
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- Archives de l'Institut Pasteur de Tunis, 2020, v. 97, n. 1-4, p. 72
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- Article
Gilbert's syndrome and the risk of death: A population-based cohort study.
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- Journal of Gastroenterology & Hepatology, 2013, v. 28, n. 10, p. 1643, doi. 10.1111/jgh.12279
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- Article
Approach to Hereditary Storage Diseases in Patients with Hepatosplenomegaly.
- Published in:
- 2015
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- Publication type:
- Abstract
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
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- 2018
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- Publication type:
- journal article
A Rare Case of Rivaroxaban Causing Delayed Symptomatic Hepatocellular Injury and Hyperbilirubinemia.
- Published in:
- 2017
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- Publication type:
- Case Study
Microarray with LNA-probes for genotyping of polymorphic variants of Gilbert's syndrome gene UGT1A1(TA)n.
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- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 6, p. 1177, doi. 10.1515/cclm-2012-0656
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- Article
High-colored plasma: a red signal for transfusion.
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- 2018
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- Publication type:
- journal article
Validation of transcutaneous bilirubin nomogram for identifying neonatal hyperbilirubinemia in healthy Chinese term and late-preterm infants: a multicenter study.
- Published in:
- Jornal de Pediatria, 2014, v. 90, n. 3, p. 273, doi. 10.1016/j.jpedp.2013.08.014
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- Publication type:
- Article
The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis.
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- Jornal de Pediatria, 2013, v. 89, n. 5, p. 434, doi. 10.1016/j.jped.2013.01.008
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- Publication type:
- Article