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Glycolytic activity and in vitro effect of the pyruvate kinase activator AG‐946 in red blood cells from low‐risk myelodysplastic syndromes patients: A proof‐of‐concept study.
- Published in:
- American Journal of Hematology, 2024, v. 99, n. 6, p. 1201, doi. 10.1002/ajh.27300
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- Publication type:
- Article
Cellular properties of human erythrocytes preserved in saline-adenine-glucose-mannitol in the presence of L-carnitine.
- Published in:
- American Journal of Hematology, 2007, v. 82, n. 1, p. 31, doi. 10.1002/ajh.20753
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- Publication type:
- Article
Clinical and molecular aspects of 23 patients affected by paroxysmal nocturnal hemoglobinuria.
- Published in:
- American Journal of Hematology, 2004, v. 77, n. 1, p. 36, doi. 10.1002/ajh.20144
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- Publication type:
- Article
Repetitive reddish discoloration of urine in a female adolescent following short-distance walking on a smooth road: Questions.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 12, p. 2253, doi. 10.1007/s00467-017-3596-5
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- Publication type:
- Article
Repetitive reddish discoloration of the urine in an adolescent female following short-distance walking on a smooth road: Answers.
- Published in:
- Pediatric Nephrology, 2017, v. 32, n. 12, p. 2255, doi. 10.1007/s00467-017-3611-x
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- Publication type:
- Article
Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.
- Published in:
- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.949044
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- Publication type:
- Article
Pyruvate Kinase Deficiency: Current Challenges and Future Prospects.
- Published in:
- Journal of Blood Medicine, 2022, v. 13, p. 461, doi. 10.2147/JBM.S353907
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- Publication type:
- Article
Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis.
- Published in:
- 2015
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- Publication type:
- journal article
An unusual febrile nonhemolytic reaction occurred after transfusion in a thalassemia major patient with asymptomatic Plasmodium falciparum infection.
- Published in:
- Transfusion, 2011, v. 51, n. 3, p. 469, doi. 10.1111/j.1537-2995.2010.02853.x
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- Publication type:
- Article
Red cell pyruvate kinase deficiency: 17 new mutations of the PK-LR gene.
- Published in:
- British Journal of Haematology, 2005, v. 129, n. 6, p. 839, doi. 10.1111/j.1365-2141.2005.05520.x
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- Publication type:
- Article
Molecular characterization of six unrelated Italian patients affected by pyrimidine 5′-nucleotidase deficiency.
- Published in:
- British Journal of Haematology, 2003, v. 122, n. 5, p. 847, doi. 10.1046/j.1365-2141.2003.04532.x
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- Publication type:
- Article
Molecular characterization of the PK-LR gene in sixteen pyruvate kinase-deficient patients.
- Published in:
- British Journal of Haematology, 2001, v. 113, n. 1, p. 43, doi. 10.1046/j.1365-2141.2001.02711.x
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- Publication type:
- Article
Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene.
- Published in:
- European Journal of Haematology, 2010, v. 85, n. 2, p. 170, doi. 10.1111/j.1600-0609.2010.01451.x
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- Publication type:
- Article
When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms.
- Published in:
- British Journal of Haematology, 2023, v. 203, n. 4, p. 684, doi. 10.1111/bjh.19038
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- Publication type:
- Article
Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years.
- Published in:
- British Journal of Haematology, 2022, v. 198, n. 5, p. 912, doi. 10.1111/bjh.18106
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- Publication type:
- Article
Iron overload in congenital haemolytic anaemias: role of hepcidin and cytokines and predictive value of ferritin and transferrin saturation.
- Published in:
- British Journal of Haematology, 2019, v. 185, n. 3, p. 523, doi. 10.1111/bjh.15811
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- Publication type:
- Article
Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlations.
- Published in:
- British Journal of Haematology, 2016, v. 175, n. 4, p. 696, doi. 10.1111/bjh.14271
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- Publication type:
- Article
Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants.
- Published in:
- Pediatric Blood & Cancer, 2023, v. 70, n. 9, p. 1, doi. 10.1002/pbc.30344
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- Publication type:
- Article
Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study.
- Published in:
- Frontiers in Physiology, 2021, v. 11, p. 1, doi. 10.3389/fphys.2021.684569
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- Publication type:
- Article
Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.
- Published in:
- Human Mutation, 2009, v. 30, n. 9, p. 1292, doi. 10.1002/humu.21077
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- Publication type:
- Article
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-31571-2
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- Publication type:
- Article
Cytokine polymorphisms in patients with autoimmune hemolytic anemia.
- Published in:
- Frontiers in Immunology, 2023, p. 01, doi. 10.3389/fimmu.2023.1221582
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- Publication type:
- Article
Hereditary red cell membrane defects: diagnostic and clinical aspects.
- Published in:
- Blood Transfusion (17232007), 2011, v. 9, n. 3, p. 274, doi. 10.2450/2011.0086-10
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- Publication type:
- Article
Congenital Hemolytic Anemias: Is There a Role for the Immune System?
- Published in:
- Frontiers in Immunology, 2020, v. 11, p. 1, doi. 10.3389/fimmu.2020.01309
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- Publication type:
- Article
Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families.
- Published in:
- Case Reports in Hematology, 2017, p. 1, doi. 10.1155/2017/2769570
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- Publication type:
- Article
Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases.
- Published in:
- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00467
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- Publication type:
- Article
A case of complete adenylate kinase deficiency due to a nonsense mutation in AK-1 gene (Arg 107 → Stop, CGA → TGA) associated with chronic haemolytic anaemia.
- Published in:
- British Journal of Haematology, 1999, v. 105, n. 1, p. 75, doi. 10.1111/j.1365-2141.1999.01297.x
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- Publication type:
- Article
A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.
- Published in:
- British Journal of Haematology, 1997, v. 98, n. 2, p. 283, doi. 10.1046/j.1365-2141.1997.1983013.x
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- Publication type:
- Article