Detalhe da pesquisa
1.
Post-transfusion biotin-labeled red blood cell survival studies in pediatric sickle cell disease with antibodies of uncertain significance.
Transfusion
; 64(5): 800-807, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38506450
2.
Survival of transfused red blood cells from a donor with alpha-thalassemia trait in a recipient with sickle cell disease.
Transfusion
; 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38693059
3.
Sites of regulated phosphorylation that control K-Cl cotransporter activity.
Cell
; 138(3): 525-36, 2009 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-19665974
4.
Extracellular fluid tonicity impacts sickle red blood cell deformability and adhesion.
Blood
; 130(24): 2654-2663, 2017 12 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-28978568
5.
Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review.
Ann Intern Med
; 169(9): 619-627, 2018 11 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30383109
6.
Losartan therapy decreases albuminuria with stable glomerular filtration and permselectivity in sickle cell anemia.
Blood Cells Mol Dis
; 69: 65-70, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28951038
7.
Sickle Mice Are Sensitive to Hypoxia/Ischemia-Induced Stroke but Respond to Tissue-Type Plasminogen Activator Treatment.
Stroke
; 48(12): 3347-3355, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29127268
8.
Normal saline is associated with increased sickle red cell stiffness and prolonged transit times in a microfluidic model of the capillary system.
Microcirculation
; 24(5)2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28106307
9.
Hydroxyurea effectiveness in children and adolescents with sickle cell anemia: A large retrospective, population-based cohort.
Am J Hematol
; 92(1): 77-81, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27761932
10.
Changes in urine albumin to creatinine ratio with the initiation of hydroxyurea therapy among children and adolescents with sickle cell disease.
Pediatr Blood Cancer
; 64(12)2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28612449
11.
Biochemical surrogate markers of hemolysis do not correlate with directly measured erythrocyte survival in sickle cell anemia.
Am J Hematol
; 91(12): 1195-1201, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27648808
12.
Covid-19 will not "magically disappear": Why access to widespread testing is paramount.
Am J Hematol
; 96(2): 174-178, 2021 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33576528
13.
Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease.
Blood
; 121(11): 2099-107, 2013 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-23349388
14.
Eculizumab for complement mediated thrombotic microangiopathy in sickle cell disease.
Haematologica
; 105(12): 2887-2891, 2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33256394
15.
Activation of protein kinase C by phorbol ester increases red blood cell scramblase activity and external phosphatidylserine.
Eur J Haematol
; 95(5): 405-10, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25600460
16.
Use of an oral stable isotope label to confirm variation in red blood cell mean age that influences HbA1c interpretation.
Am J Hematol
; 90(1): 50-55, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25293624
17.
Pharmacological inhibition of calpain-1 prevents red cell dehydration and reduces Gardos channel activity in a mouse model of sickle cell disease.
FASEB J
; 27(2): 750-9, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23085996
18.
Angiogenic growth factors augment K-Cl cotransporter expression in erythroid cells via hypoxia-inducible factor-1α.
Am J Hematol
; 89(3): 273-81, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24227191
19.
Contribution of alternative complement pathway to delayed hemolytic transfusion reaction in sickle cell disease.
Haematologica
; 103(10): e483-e485, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29794144
20.
Hereditary xerocytosis: Diagnostic considerations.
Am J Hematol
; 93(3): E67-E69, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29210095