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Effect of UDP‐glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome.
- Published in:
- Kaohsiung Journal of Medical Sciences, 2019, v. 35, n. 7, p. 432, doi. 10.1002/kjm2.12077
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- Article
Bilirubin concentrations in thalassemia heterozygotes in university students.
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- European Journal of Haematology, 2011, v. 86, n. 4, p. 317, doi. 10.1111/j.1600-0609.2011.01578.x
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- Article
Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants.
- Published in:
- American Journal of Hematology, 1996, v. 51, n. 1, p. 19, doi. 10.1002/(SICI)1096-8652(199601)51:1<19::AID-AJH4>3.0.CO;2-A
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- Article
Diagnosis of Glucose-6-Phosphate Dehydrogenase (G6PD) Mutations by DNA Amplification and Allele-Specific Oligonucleotide Probes.
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- Acta Haematologica, 1992, v. 88, n. 2/3, p. 92, doi. 10.1159/000204659
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- Article
Bilirubin metabolism and UDP‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response.
- Published in:
- Kaohsiung Journal of Medical Sciences, 2022, v. 38, n. 8, p. 729, doi. 10.1002/kjm2.12579
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- Article
Content of reduced glutathione and consequences in recipients of glucose-6-phosphate dehydrogenase deficient red blood cells.
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- American Journal of Hematology, 1998, v. 57, n. 3, p. 187, doi. 10.1002/(SICI)1096-8652(199803)57:3<187::AID-AJH1>3.0.CO;2-R
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- Article
G6PD NanKang (517 T→C; 173 Phe→Leu): A New Chinese G6PD Variant Associated with Neonatal Jaundice.
- Published in:
- Human Heredity, 1996, v. 46, n. 4, p. 201, doi. 10.1159/000154354
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- Article