Detalles de la búsqueda
1.
CEBPA-double-mutated acute myeloid leukemia displays a unique phenotypic profile: a reliable screening method and insight into biological features.
Haematologica
; 102(3): 529-540, 2017 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28250006
2.
Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria.
Haematologica
; 99(2): 262-6, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24038027
3.
Easy genotyping of complement C3 'slow' and 'fast' allotypes by tetra-primer amplification refractory mutation system PCR.
Mol Cell Probes
; 24(6): 401-2, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-20655380
4.
Severe hypoxia selects hematopoietic progenitors with stem cell potential from primary Myelodysplastic syndrome bone marrow cell cultures.
Oncotarget
; 9(12): 10561-10571, 2018 Feb 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-29535827
5.
Eculizumab treatment: stochastic occurrence of C3 binding to individual PNH erythrocytes.
J Hematol Oncol
; 10(1): 126, 2017 06 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-28629435
6.
Multilineage dysplasia as assessed by immunophenotype has no impact on clinical-biological features and outcome of NPM1-mutated acute myeloid leukemia.
Exp Hematol
; 43(10): 869-879.e22, 2015 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-26101160
7.
The frequency of granulocytes with spontaneous somatic mutations: a wide distribution in a normal human population.
PLoS One
; 8(1): e54046, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23342069
8.
Diagnosis of a T-lineage acute lymphoblastic leukemia through digitalized cell analysis of the pleural effusion.
Int Med Case Rep J
; 6: 77-80, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24204177
Resultados
1 -
8
de 8
1
Próxima >
>>