Detalhe da pesquisa
1.
How Many Tests Does It Take to Diagnose a Triple-Hit B-Lymphoblastic Lymphoma? (Hint, It's A Lot).
Pediatr Dev Pathol
; 27(2): 193-197, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38032739
2.
Multicenter study of pediatric Epstein-Barr virus-negative monomorphic post solid organ transplant lymphoproliferative disorders.
Cancer
; 129(5): 780-789, 2023 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36571557
3.
Burkitt lymphoma after solid-organ transplant: Treatment and outcomes in the paediatric PTLD collaborative.
Br J Haematol
; 200(3): 297-305, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36454546
4.
Characterization of HLH-like manifestations as a CRS variant in patients receiving CD22 CAR T cells.
Blood
; 138(24): 2469-2484, 2021 12 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-34525183
5.
Comprehensive molecular and clinical characterization of NUP98 fusions in pediatric acute myeloid leukemia.
Haematologica
; 108(8): 2044-2058, 2023 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36815378
6.
Pathologic, cytogenetic, and molecular features of acute myeloid leukemia with megakaryocytic differentiation: A report from the Children's Oncology Group.
Pediatr Blood Cancer
; 70(5): e30251, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36789545
7.
A Malignant Mimicker: Features of Kikuchi-Fujimoto Disease in the Pediatric Population.
Pediatr Dev Pathol
; 25(5): 538-547, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35583198
8.
Clinical, immunophenotypic and genomic findings of NK lymphoblastic leukemia: a study from the Bone Marrow Pathology Group.
Mod Pathol
; 34(7): 1358-1366, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33526873
9.
Lineage Switch in an Infant B-Lymphoblastic Leukemia With t(1;11)(p32;q23); KMT2A/EPS15, Following Blinatumomab Therapy.
Pediatr Dev Pathol
; 24(4): 378-382, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33749383
10.
Effects of Tumor Necrosis Factor Alpha Inhibitors on Lymph Node and Ileocecal Mucosa-Associated Lymphoid Tissue Architecture in Patients With Inflammatory Bowel Disease.
Pediatr Dev Pathol
; 23(2): 115-120, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31362580
11.
IRF4 translocation status in pediatric follicular and diffuse large B-cell lymphoma patients enrolled in Children's Oncology Group trials.
Pediatr Blood Cancer
; 66(8): e27770, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31012208
12.
Bone Marrow Morphology Associated With Germline RUNX1 Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy.
Pediatr Dev Pathol
; 22(4): 315-328, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30600763
13.
An analysis of blastic plasmacytoid dendritic cell neoplasm with translocations involving the MYC locus identifies t(6;8)(p21;q24) as a recurrent cytogenetic abnormality.
Histopathology
; 73(5): 767-776, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-29884995
14.
Classification of Preterm Birth With Placental Correlates.
Pediatr Dev Pathol
; 21(6): 548-560, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29759046
15.
How Rare Is an Oral Presentation of Myeloid Sarcoma in the Infant?
J Oral Maxillofac Surg
; 76(3): 561-568, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28943463
16.
A study of the mutational landscape of pediatric-type follicular lymphoma and pediatric nodal marginal zone lymphoma.
Mod Pathol
; 29(10): 1212-20, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27338637
17.
Heme oxygenase-1 confers protection and alters T-cell populations in a mouse model of neonatal intestinal inflammation.
Pediatr Res
; 77(5): 640-8, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25665053
18.
Mutations in mitochondrial histidyl tRNA synthetase HARS2 cause ovarian dysgenesis and sensorineural hearing loss of Perrault syndrome.
Proc Natl Acad Sci U S A
; 108(16): 6543-8, 2011 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-21464306
19.
Heme oxygenase-1 deficiency promotes the development of necrotizing enterocolitis-like intestinal injury in a newborn mouse model.
Am J Physiol Gastrointest Liver Physiol
; 304(11): G991-G1001, 2013 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23578787
20.
Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome.
Am J Hum Genet
; 87(2): 282-8, 2010 Aug 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-20673864