Detalhe da pesquisa
1.
ROS1 Alterations as a Potential Driver of Gliomas in Infant, Pediatric, and Adult Patients.
Mod Pathol
; 36(11): 100294, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37532182
2.
Agminated presentation of fusion-driven melanocytic neoplasms.
J Cutan Pathol
; 50(10): 913-921, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37407520
3.
Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype-phenotype correlation in congenital central hypoventilation syndrome (CCHS).
Genet Med
; 23(9): 1656-1663, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33958749
4.
Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report.
BMC Infect Dis
; 21(1): 740, 2021 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34344305
5.
The Essentials of Molecular Testing in CNS Tumors: What to Order and How to Integrate Results.
Curr Neurol Neurosci Rep
; 20(7): 23, 2020 05 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32445025
6.
Inv(11)(q21q23); KMT2A-MAML2, a Recurrent Genetic Abnormality in T-Cell Therapy-related Acute Lymphoblastic Leukemia.
J Pediatr Hematol Oncol
; 42(4): e258-e261, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31343482
7.
Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family members.
Am J Med Genet A
; 179(3): 503-506, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30672101
8.
The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing.
Cancer
; 124(16): 3381-3389, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29905933
9.
Variant allelic frequency of driver mutations predicts success of genomic DNA methylation classification in central nervous system tumors.
Acta Neuropathol
; 145(3): 365-367, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36700952
10.
Lineage switch from acute myeloid leukemia to B-lymphoblastic lymphoma with an acquired PIK3R1 loss-of-function mutation.
Am J Hematol
; 98(1): E1-E3, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36288429
11.
Clinical and Electroencephalographic Characteristics of Infantile-Onset Epilepsies Caused by Genetic Mutations.
J Pediatr
; 184: 172-177.e1, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28410084
12.
Early mixed T-cell chimerism is predictive of pediatric AML or MDS relapse after hematopoietic stem cell transplant.
Pediatr Blood Cancer
; 64(9)2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28266766
13.
ALK-rearranged renal cell carcinomas in children.
Genes Chromosomes Cancer
; 55(5): 442-51, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26773439
14.
Primary Cutaneous Mammary Analog Secretory Carcinoma With ETV6-NTRK3 Translocation.
Am J Dermatopathol
; 38(11): 842-845, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27763904
15.
CD4 T cell-restricted IL-2 signaling defect in a patient with a novel IFNGR1 deficiency.
J Allergy Clin Immunol
; 141(1): 435-439.e7, 2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28927822
16.
Uncommon molecular alterations in follicular-derived thyroid carcinoma: A single institution study.
Pathol Res Pract
; 258: 155355, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38763089
17.
Supernatant fluid from endobronchial ultrasound-guided transbronchial needle aspiration for rapid next-generation sequencing.
J Am Soc Cytopathol
; 2024 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-38797657
18.
Integration of individualized and population-level molecular epidemiology data to model COVID-19 outcomes.
Cell Rep Med
; 5(1): 101361, 2024 01 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-38232695
19.
Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: a report from the Children's Oncology Group.
Cancer
; 119(21): 3887-94, 2013 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23983061
20.
BRAF Exon 15 Mutations in the Evaluation of Well-Differentiated Epithelial Nephroblastic Neoplasms in Children: A Report From the Children's Oncology Group Study AREN03B2.
Arch Pathol Lab Med
; 2023 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38116848