Detalhe da pesquisa
1.
Clofarabine increases the eradication of minimal residual disease of primary B-precursor acute lymphoblastic leukemia compared to high-dose cytarabine without improvement of outcome. Results from the randomized clinical trial 08-09 of the Cooperative Acute Lymphoblastic Leukemia Study Group.
Haematologica
; 107(5): 1026-1033, 2022 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34348455
2.
High sensitivity and clonal stability of the genomic fusion as single marker for response monitoring in ETV6-RUNX1-positive acute lymphoblastic leukemia.
Pediatr Blood Cancer
; 66(8): e27780, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31034759
3.
Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoire.
Eur J Immunol
; 47(2): 364-373, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27925643
4.
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome.
Blood
; 127(8): 997-1006, 2016 Feb 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-26744459
5.
Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease.
Pediatr Blood Cancer
; 65(11): e27344, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30070073
6.
Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis.
J Clin Immunol
; 37(8): 770-780, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28936583
7.
Lineage switch under blinatumomab treatment of relapsed common acute lymphoblastic leukemia without MLL rearrangement.
Pediatr Blood Cancer
; 64(11)2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28453885
8.
Malignancy-associated haemophagocytic lymphohistiocytosis in children and adolescents.
Br J Haematol
; 170(4): 539-49, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25940575
9.
Novel Patient with Late-Onset Familial Hemophagocytic Lymphohistiocytosis with STXBP2 Mutations Presenting with Autoimmune Hepatitis, Neurological Manifestations and Infections Associated with Hypogammaglobulinemia.
J Clin Immunol
; 35(1): 22-5, 2015 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25491289
10.
Hemophagocytic lymphohistiocytosis in syntaxin-11-deficient mice: T-cell exhaustion limits fatal disease.
Blood
; 121(4): 604-13, 2013 Jan 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-23190531
11.
The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2.
Blood
; 121(15): 2943-51, 2013 Apr 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-23403622
12.
Ulceration in Prolidase Deficiency: Successful Treatment with Anticoagulants.
Acta Derm Venereol
; 100(1): adv00002, 2020 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31573664
13.
Syntaxin 11 is required for NK and CD8⺠T-cell cytotoxicity and neutrophil degranulation.
Eur J Immunol
; 43(1): 194-208, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-23042080
14.
A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.
Blood
; 119(12): 2754-63, 2012 Mar 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22294731
15.
Distinct mutations in STXBP2 are associated with variable clinical presentations in patients with familial hemophagocytic lymphohistiocytosis type 5 (FHL5).
Blood
; 119(25): 6016-24, 2012 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22451424
16.
Clofarabine in combination with pegylated asparaginase in the frontline treatment of childhood acute lymphoblastic leukaemia: a feasibility report from the CoALL 08-09 trial.
Br J Haematol
; 163(2): 240-7, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23937310
17.
Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome.
Blood
; 118(17): 4620-9, 2011 Oct 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-21878672
18.
Persistent defective membrane trafficking in epithelial cells of patients with familial hemophagocytic lymphohistiocytosis type 5 due to STXBP2/MUNC18-2 mutations.
Pediatr Blood Cancer
; 60(7): 1215-22, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23382066
19.
Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation.
J Allergy Clin Immunol
; 140(6): 1721-1724, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28633876
20.
Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11.
Am J Hum Genet
; 85(4): 482-92, 2009 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-19804848