Found: 15
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Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia.
- Published in:
- Clinical Genetics, 1994, v. 46, n. 5, p. 357, doi. 10.1111/j.1399-0004.1994.tb04178.x
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- Article
Red Blood Cell Enzyme Disorders: An Overview.
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- Pediatric Annals, 2008, v. 37, n. 5, p. 303, doi. 10.3928/00904481-20080501-08
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- Publication type:
- Article
Epidemiological shift of glucose-6-phosphate dehydrogenase mutations in northern Italy in the last 15 years.
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- Annals of Hematology, 2021, v. 100, n. 11, p. 2683, doi. 10.1007/s00277-021-04630-9
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- Article
Cholelithiasis in thalassemia major.
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- European Journal of Haematology, 2009, v. 82, n. 1, p. 22, doi. 10.1111/j.1600-0609.2008.01162.x
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- Article
UGT1A1 genotype does not affect tyrosine kinase inhibitors efficacy and safety in chronic myeloid leukemia.
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- American Journal of Hematology, 2019, v. 94, n. 11, p. E283, doi. 10.1002/ajh.25596
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- Article
Circulating cell‐free DNA and ineffective erythropoiesis in nontransfusion‐dependent β‐thalassemia.
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- American Journal of Hematology, 2018, v. 93, n. 11, p. E365, doi. 10.1002/ajh.25248
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- Article
Laboratory Diagnosis of Porphyria.
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- Diagnostics (2075-4418), 2021, v. 11, n. 8, p. 1343, doi. 10.3390/diagnostics11081343
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- Article
HFE genotype influences erythropoiesis support requirement in hemodialysis patients: a prospective study.
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- 2008
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- Publication type:
- journal article
Membrane-bound iron contributes to oxidative damage of β-thalassaemia intermedia erythrocytes.
- Published in:
- British Journal of Haematology, 2001, v. 112, n. 1, p. 48, doi. 10.1046/j.1365-2141.2001.02482.x
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- Article
A novel polymorphism (219G>A) in the transferrin receptor gene.
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- Human Mutation, 2000, v. 15, n. 4, p. 389, doi. 10.1002/(SICI)1098-1004(200004)15:4<389::AID-HUMU28>3.0.CO;2-H
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- Article
Porphyrias at a glance: diagnosis and treatment.
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- Internal & Emergency Medicine, 2010, v. 5, p. 73, doi. 10.1007/s11739-010-0449-7
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- Publication type:
- Article
THE INTERACTION BETWEEN GILBERT'S SYNDROME AND G6PD DEFICIENCY INFLUENCES BILIRUBIN LEVELS.
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- British Journal of Haematology, 1999, v. 104, n. 4, p. 928, doi. 10.1111/j.1365-2141.1999.1331a.x
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- Publication type:
- Article
Metabolic indicators of oxidative stress correlate with haemichrome attachment to membrane, band 3 aggregation and erythrophagocytosis in β-thalassaemia intermedia.
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- British Journal of Haematology, 1999, v. 104, n. 3, p. 504, doi. 10.1046/j.1365-2141.1999.01217.x
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- Publication type:
- Article
Biochemical and molecular characterization of a new sporadic glucose-6-phosphate dehydrogenase variant described in Italy: G6PD Modena.
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- British Journal of Haematology, 1994, v. 87, n. 1, p. 209, doi. 10.1111/j.1365-2141.1994.tb04896.x
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- Publication type:
- Article
Hyperferritinemia, Iron Overload, and Multiple Metabolic Alterations Identify Patients at Risk for Nonalcoholic Steatohepatitis.
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- American Journal of Gastroenterology (Springer Nature), 2001, v. 96, n. 8, p. 2448, doi. 10.1111/j.1572-0241.2001.04052.x
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- Publication type:
- Article