Detalhe da pesquisa
1.
Base editing of haematopoietic stem cells rescues sickle cell disease in mice.
Nature
; 595(7866): 295-302, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34079130
2.
Erythroblastic islands foster granulopoiesis in parallel to terminal erythropoiesis.
Blood
; 140(14): 1621-1634, 2022 10 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35862735
3.
Red cell abnormalities characterized by ektacytometry in children with cholestasis.
Pediatr Res
; 95(4): 1035-1040, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38040987
4.
Rapid measurement of hemoglobin-oxygen dissociation by leveraging Bohr effect and Soret band bathochromic shift.
Analyst
; 149(9): 2561-2572, 2024 Apr 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38501195
5.
Navigating the marrow sea towards erythromyeloblastic islands under normal and inflammatory conditions.
Curr Opin Hematol
; 30(3): 80-85, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36718814
6.
Crosstalk between terminal erythropoiesis and granulopoiesis within their common niche: the erythromyeloblastic island.
Curr Opin Hematol
; 30(4): 99-105, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254853
7.
VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects.
Am J Hum Genet
; 107(6): 1149-1156, 2020 12 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33186543
8.
Etavopivat, a Pyruvate Kinase Activator in Red Blood Cells, for the Treatment of Sickle Cell Disease.
J Pharmacol Exp Ther
; 380(3): 210-219, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35031585
9.
Red cell membrane disorders: structure meets function.
Blood
; 136(11): 1250-1261, 2020 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32702754
10.
Altered erythropoiesis in newborns with congenital heart disease.
Pediatr Res
; 91(3): 606-611, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33531673
11.
Early initiation of hydroxyurea (hydroxycarbamide) using individualised, pharmacokinetics-guided dosing can produce sustained and nearly pancellular expression of fetal haemoglobin in children with sickle cell anaemia.
Br J Haematol
; 194(3): 617-625, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-34227124
12.
Rasa3 regulates stage-specific cell cycle progression in murine erythropoiesis.
Blood Cells Mol Dis
; 87: 102524, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33341069
13.
Congenital dyserythropoietic anemia type I: First report from the Congenital Dyserythropoietic Anemia Registry of North America (CDAR).
Blood Cells Mol Dis
; 87: 102534, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33401150
14.
Implementation of near-universal hydroxyurea uptake among children with sickle cell anemia: A single-center experience.
Pediatr Blood Cancer
; 68(6): e29008, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33742510
15.
How I approach hereditary hemolytic anemia and splenectomy.
Pediatr Blood Cancer
; 67(11): e28337, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32391969
16.
RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis.
Blood
; 130(Suppl_1): 8, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31940662
17.
Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis.
Blood
; 130(16): 1845-1856, 2017 10 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-28716860
18.
Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.
Am J Hematol
; 94(8): 871-879, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31106898
19.
Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency.
Am J Hematol
; 94(1): 149-161, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30358897
20.
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity.
Pediatr Blood Cancer
; 66(2): e27531, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30393954