Found: 19
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Hemolysis and Hyperbilirubinemia in an African American Neonate Heterozygous for Glucose-6-Phosphate Dehydrogenase Deficiency.
- Published in:
- Journal of Perinatology, 2002, v. 22, n. 7, p. 577, doi. 10.1038/sj.jp.7210769
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- Publication type:
- Article
Early non-neutralizing, afucosylated antibody responses are associated with COVID-19 severity.
- Published in:
- Science Translational Medicine, 2022, v. 14, n. 635, p. 1, doi. 10.1126/scitranslmed.abm7853
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- Publication type:
- Article
Antibodies elicited by SARS-CoV-2 infection or mRNA vaccines have reduced neutralizing activity against Beta and Omicron pseudoviruses.
- Published in:
- Science Translational Medicine, 2022, v. 14, n. 634, p. 1, doi. 10.1126/scitranslmed.abn7842
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- Publication type:
- Article
The effect of HFE genotypes on measurements of iron overload in patients attending a health appraisal clinic.
- Published in:
- 2000
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- Publication type:
- journal article
SLC40A1 c.1402G→A Results in Aberrant Splicing, Ferroportin Truncation after Glycine 330, and an Autosomal Dominant Hemochromatosis Phenotype.
- Published in:
- Acta Haematologica, 2007, v. 118, n. 4, p. 237, doi. 10.1159/000112830
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- Publication type:
- Article
Soluble Transferrin Receptor-1 Levels in Mice Do Not Affect Iron Absorption.
- Published in:
- Acta Haematologica, 2006, v. 116, n. 4, p. 249, doi. 10.1159/000095875
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- Publication type:
- Article
Relationship between Molecular Variants and Clinical Manifestions in Twelve Glucose-6-Phosphate Dehydrogenase-Deficient Patients in Jordan.
- Published in:
- Acta Haematologica, 2005, v. 114, n. 2, p. 125, doi. 10.1159/000086589
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- Publication type:
- Article
Relationship of Body Iron Stores to Levels of Serum Ferritin, Serum Iron, Unsaturated Iron Binding Capacity and Transferrin Saturation in Patients with Iron Storage Disease.
- Published in:
- Acta Haematologica, 2002, v. 107, n. 3, p. 145, doi. 10.1159/000057632
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- Publication type:
- Article
Three Gaucher-Disease-Producing Mutations in a Patient with Gaucher Disease: Mechanism and Diagnostic Implications.
- Published in:
- Acta Haematologica, 2000, v. 104, n. 2/3, p. 103, doi. 10.1159/000039760
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- Publication type:
- Article
Effect of Ozone on Red Blood Cell Enzymes and Intermediates.
- Published in:
- Acta Haematologica, 1999, v. 102, n. 3, p. 148, doi. 10.1159/000040990
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- Publication type:
- Article
G-6-PD Walter Reed: Possible insight into 'structural' NADP in G-6-PD.
- Published in:
- American Journal of Hematology, 1986, v. 23, n. 1, p. 25, doi. 10.1002/ajh.2830230105
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- Publication type:
- Article
Glucocerebrosidase (Gaucher disease).
- Published in:
- Human Mutation, 1996, v. 8, n. 3, p. 207, doi. 10.1002/(SICI)1098-1004(1996)8:3<207::AID-HUMU2>3.0.CO;2-6
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- Publication type:
- Article
Erroneous assignment of Gaucher disease genotype as a consequence of a complete gene deletion.
- Published in:
- Human Mutation, 1994, v. 4, n. 3, p. 212, doi. 10.1002/humu.1380040307
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- Publication type:
- Article
Gaucher disease mutations in non-Jewish patients.
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- British Journal of Haematology, 1993, v. 85, n. 2, p. 401, doi. 10.1111/j.1365-2141.1993.tb03185.x
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- Publication type:
- Article
Blood cell phosphogluconolactonase: assay and properties.
- Published in:
- British Journal of Haematology, 1986, v. 62, n. 3, p. 577, doi. 10.1111/j.1365-2141.1986.tb02970.x
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- Publication type:
- Article
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's disease.
- Published in:
- Movement Disorders, 2002, v. 17, n. 6, p. 1302, doi. 10.1002/mds.10253
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- Publication type:
- Article
Suppression of the hepcidin-encoding gene Hamp permits iron overload in mice lacking both hemojuvelin and matriptase-2/TMPRSS6.
- Published in:
- British Journal of Haematology, 2009, v. 147, n. 4, p. 571, doi. 10.1111/j.1365-2141.2009.07873.x
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- Publication type:
- Article
Haematological effects of the C282Y HFE mutation in homozygous and heterozygous states among subjects of northern and southern European ancestry.
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- British Journal of Haematology, 2003, v. 120, n. 5, p. 887, doi. 10.1046/j.1365-2141.2003.04215.x
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- Publication type:
- Article
Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies.
- Published in:
- British Journal of Haematology, 2001, v. 112, n. 2, p. 475, doi. 10.1046/j.1365-2141.2001.02526.x
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- Publication type:
- Article