Detalhe da pesquisa
1.
A case-control study of bleeding risk in children with 22q11.2 deletion syndrome undergoing cardiac surgery.
Platelets
; 35(1): 2290108, 2024 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38099325
2.
Genetic variants in toll-like receptor 4 are associated with lack of steroid-responsiveness in pediatric ITP patients.
Am J Hematol
; 95(4): 395-400, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31903617
3.
Association of a positive direct antiglobulin test with chronic immune thrombocytopenia and use of second line therapies in children: A multi-institutional review.
Am J Hematol
; 94(4): 461-466, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30663792
4.
The 22q11.2 deletion syndrome: Cancer predisposition, platelet abnormalities and cytopenias.
Am J Med Genet A
; 176(10): 2121-2127, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28940864
5.
Racial variation in ITP prevalence and chronic disease phenotype suggests biological differences.
Blood
; 136(5): 640-643, 2020 07 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-32559763
6.
2-O, 3-O desulfated heparin mitigates murine chemotherapy- and radiation-induced thrombocytopenia.
Blood Adv
; 2(7): 754-761, 2018 04 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29599195