Detalhe da pesquisa
1.
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.
Am J Hematol
; 99(6): 1201-1204, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38563490
2.
Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years.
Br J Haematol
; 198(5): 912-915, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35277856
3.
Rasburicase-induced Methemoglobinemia: A Case Report and Literature Review.
J Pediatr Hematol Oncol
; 43(6): e886-e890, 2021 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33122582
4.
Iron overload in congenital haemolytic anaemias: role of hepcidin and cytokines and predictive value of ferritin and transferrin saturation.
Br J Haematol
; 185(3): 523-531, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30828802
5.
When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms.
Br J Haematol
; 203(4): 684-687, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37565283
6.
Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants.
Pediatr Blood Cancer
; : e30344, 2023 Apr 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37057369
7.
A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to Heat.
J Pediatr Hematol Oncol
; 40(7): e458-e460, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29309376
8.
Detection of red blood cell antibodies in mitogen-stimulated cultures from patients with hereditary spherocytosis.
Transfusion
; 55(12): 2930-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26259504
9.
A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemia.
Clin Lab
; 59(3-4): 421-4, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23724634
10.
Cytokine polymorphisms in patients with autoimmune hemolytic anemia.
Front Immunol
; 14: 1221582, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38022547
11.
Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency.
Sci Rep
; 13(1): 4395, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-36927785
12.
A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: molecular and functional characterization.
Mol Genet Metab
; 106(4): 455-61, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22705348
13.
Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics.
Haematologica
; 97(4): 516-23, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22058213
14.
Pyruvate Kinase Deficiency: Current Challenges and Future Prospects.
J Blood Med
; 13: 461-471, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36072510
15.
Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis.
Front Physiol
; 13: 949044, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36035481
16.
Case report: Transfusion independence and abolition of extravascular hemolysis in a PNH patient treated with pegcetacoplan.
Front Immunol
; 13: 1060923, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36532073
17.
Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study.
Front Physiol
; 12: 684569, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34093240
18.
CDAII presenting as hydrops foetalis: molecular characterization of two cases.
Blood Cells Mol Dis
; 45(1): 20-2, 2010 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20381388
19.
Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene.
Eur J Haematol
; 85(2): 170-3, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20374271
20.
Congenital Hemolytic Anemias: Is There a Role for the Immune System?
Front Immunol
; 11: 1309, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32655575