Inherited Unconjugated Hyperbilirubinemias and Radical Cancer Surgery: Perioperative Concerns for Bilateral Modified Radical Mastectomy.
- Published in:
- Archives of Anesthesiology & Critical Care, 2022, v. 8, n. 4, p. 336
- By:
- Publication type:
- Article
Works matching DE "HEREDITARY hyperbilirubinemia"
Results: 16
1
2
A Rare Case of Rivaroxaban Causing Delayed Symptomatic Hepatocellular Injury and Hyperbilirubinemia.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
3
High-colored plasma: a red signal for transfusion.
- Published in:
- 2018
- By:
- Publication type:
- journal article
4
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
- By:
- Publication type:
- Article
5
The impact of SLCO1B1 genetic polymorphisms on neonatal hyperbilirubinemia: a systematic review with meta-analysis.
- Published in:
- Jornal de Pediatria, 2013, v. 89, n. 5, p. 434, doi. 10.1016/j.jped.2013.01.008
- By:
- Publication type:
- Article
6
Perioperative management of a patient with Gilberts syndrome and rheumatic heart disease.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
7
Microarray with LNA-probes for genotyping of polymorphic variants of Gilbert's syndrome gene UGT1A1(TA)n.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 6, p. 1177, doi. 10.1515/cclm-2012-0656
- By:
- Publication type:
- Article
8
Radionuclide cholescintigraphy in genetically confirmed Rotor syndrome.
- Published in:
- Pediatrics International, 2015, v. 57, n. 5, p. 981, doi. 10.1111/ped.12676
- By:
- Publication type:
- Article
9
Two Different UGT1A1 Mutations causing Crigler-Najjar Syndrome types I and II in an Iranian Family.
- Published in:
- 2015
- By:
- Publication type:
- Case Study
10
The Prevalence of Abnormal Cerebro-Placental Doppler Indices Ratio [CPR] in Hypertensive Disorders of Pregnancy.
- Published in:
- Journal of the Medical Association of Thailand, 2018, v. 101, n. 8, p. 1025
- By:
- Publication type:
- Article
11
Case report: multiple UGT1A1 gene variants in a patient with Crigler-Najjar syndrome.
- Published in:
- 2018
- By:
- Publication type:
- journal article
12
The first Turkish family with Rotor syndrome diagnosed at the molecular level.
- Published in:
- Türk Pediatri Arşivi, 2020, v. 55, n. 4, p. 430, doi. 10.14744/TurkPediatriArs.2019.55798
- By:
- Publication type:
- Article
13
GENOTYPE-PHENOTYPE CORRELATION IN TUNISIAN RETT SYNDROME PATIENTS.
- Published in:
- Archives de l'Institut Pasteur de Tunis, 2020, v. 97, n. 1-4, p. 72
- By:
- Publication type:
- Article
14
Approach to Hereditary Storage Diseases in Patients with Hepatosplenomegaly.
- Published in:
- 2015
- By:
- Publication type:
- Abstract
15
Diagnostic criteria and contributors to Gilbert’s syndrome.
- Published in:
- Critical Reviews in Clinical Laboratory Sciences, 2018, v. 55, n. 2, p. 129, doi. 10.1080/10408363.2018.1428526
- By:
- Publication type:
- Article
16
Gilbert's syndrome and the risk of death: A population-based cohort study.
- Published in:
- Journal of Gastroenterology & Hepatology, 2013, v. 28, n. 10, p. 1643, doi. 10.1111/jgh.12279
- By:
- Publication type:
- Article