Detalhe da pesquisa
1.
Mild dyserythropoiesis and ß-like globin gene expression imbalance due to the loss of histone chaperone ASF1B.
Hum Genomics
; 14(1): 39, 2020 10 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-33066815
2.
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with ß-Thalassemia Trait Results in Severe Hemolytic Anemia.
Hemoglobin
; 43(2): 77-82, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31190578
3.
Residual pyruvate kinase activity in PKLR-deficient erythroid precursors of a patient suffering from severe haemolytic anaemia.
Eur J Haematol
; 98(6): 584-589, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28295642
4.
Rh-null phenotype and stomatocytosis.
Br J Haematol
; 194(5): 803, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33901315
5.
Rapid diagnosis of hereditary haemolytic anaemias using automated rheoscopy and supervised machine learning.
Br J Haematol
; 190(4): e250-e255, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32627174
6.
Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis.
Am J Hematol
; 90(3): E35-9, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25388786
7.
Two novel haemoglobin variants that affect haemoglobin A1c measurement by ion-exchange chromatography.
Clin Chem Lab Med
; 53(9): 1465-71, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26035110
8.
Hemoglobin analyses in the Netherlands reveal more than 80 different variants including six novel ones.
Hemoglobin
; 38(1): 1-7, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24200101
9.
The Gardos effect drives erythrocyte senescence and leads to Lu/BCAM and CD44 adhesion molecule activation.
Blood Adv
; 4(24): 6218-6229, 2020 12 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-33351118
10.
Comparison of Spectrophotometry, Chromate Inhibition, and Cytofluorometry Versus Gene Sequencing for Detection of Heterozygously Glucose-6-Phosphate Dehydrogenase-Deficient Females.
J Histochem Cytochem
; 65(11): 627-636, 2017 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-28902532
11.
Intrinsic defects in erythroid cells from familial hemophagocytic lymphohistiocytosis type 5 patients identify a role for STXBP2/Munc18-2 in erythropoiesis and phospholipid scrambling.
Exp Hematol
; 43(12): 1072-1076.e2, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26320718