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1.
Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen-sensing pathway from primary familial and congenital polycythaemia.
Br J Haematol;
202(3): 674-685, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-37246471
2.
Czech and Slovak Diamond-Blackfan Anemia (DBA) Registry update: Clinical data and novel causative genetic lesions.
Blood Cells Mol Dis;
81: 102380, 2020 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-31855845
3.
Two novel mutations (p.(Ser160Pro) and p.(Arg472Cys)) causing glucose-6-phosphate isomerase deficiency are associated with erythroid dysplasia and inappropriately suppressed hepcidin.
Blood Cells Mol Dis;
69: 23-29, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28803808
4.
Molecular Characterization of ß-Thalassemia in the Czech and Slovak Populations: Mediterranean, Asian and Unique Mutations.
Hemoglobin;
40(3): 156-62, 2016 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-26956563
5.
[The prospects for children with acute lymphoblastic leukemia of being cured has increased in the Czech Republic in the 21st century to 90% - outcome of the ALL-IC BFM 2002 trial]. / Sance na vylécení detí s akutní lymfoblastickou leukémií stoupla v Ceské republicev 21. století na 90 % - výsledky studie ALL IC-BFM 2002.
Cas Lek Cesk;
154(2): 79-89, 2015.
Artículo
en Checo
| MEDLINE | ID: mdl-25994910
6.
Minimal residual disease in peripheral blood at day 15 identifies a subgroup of childhood B-cell precursor acute lymphoblastic leukemia with superior prognosis.
Haematologica;
96(12): 1815-21, 2011 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-21880630
7.
Prognosis of children with mixed phenotype acute leukemia treated on the basis of consistent immunophenotypic criteria.
Haematologica;
95(6): 928-35, 2010 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-20145275
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