Detalhe da pesquisa
1.
Identification of a robust DNA methylation signature for Fanconi anemia.
Am J Hum Genet
; 110(11): 1938-1949, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37865086
2.
Spindle cell lesions with oncogenic EGFR kinase domain aberrations: expanding the spectrum of protein kinase-related mesenchymal tumors.
Mod Pathol
; : 100539, 2024 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38880352
3.
PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven Cases.
Mod Pathol
; 37(2): 100387, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38007157
4.
Growing teratoma syndrome in children and adolescents: Prevalence and surgical outcome.
Pediatr Blood Cancer
; 71(8): e31126, 2024 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-38837659
5.
Role of 18F-Fluorodeoxyglucose Positron Emission Tomography in Children With Germ Cell Tumor After Chemotherapy.
J Pediatr Hematol Oncol
; 46(5): e272-e276, 2024 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38912835
6.
Pediatric BCOR-Altered Tumors From Soft Tissue/Kidney Display Specific DNA Methylation Profiles.
Mod Pathol
; 36(2): 100039, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36853789
7.
Delineation of a KDM2B-related neurodevelopmental disorder and its associated DNA methylation signature.
Genet Med
; 25(1): 49-62, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36322151
8.
Optimizing reirradiation for relapsed medulloblastoma: identifying the ideal patient and tumor profiles.
J Neurooncol
; 163(3): 577-586, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37326761
9.
Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging.
Am J Hum Genet
; 105(3): 493-508, 2019 09 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31447100
10.
Paediatric astroblastoma-like neuroepithelial tumour of the spinal cord with a MAMLD1-BEND2 rearrangement.
Neuropathol Appl Neurobiol
; 48(5): e12814, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35301744
11.
Posterior fossa ependymoma in neurodevelopmental syndrome caused by a de novo germline pathogenic POLR2A variant.
Am J Med Genet A
; 188(9): 2796-2802, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689525
12.
Cerebellar liponeurocytoma in an elderly patient: DNA methylation profiling as a helpful diagnostic tool.
Clin Neuropathol
; 41(1): 12-17, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34672257
13.
Cerebellar liponeurocytoma: clinical, histopathological and molecular features of a series of three cases, including one recurrent tumor.
Neuropathology
; 42(3): 169-180, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35042275
14.
Mesenchymal PLAG1 Tumor With PCMTD1-PLAG1 Fusion in an Infant: A New Type of "Plagoma".
Am J Dermatopathol
; 44(1): 54-57, 2022 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34291746
15.
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome.
Int J Mol Sci
; 23(3)2022 Feb 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35163737
16.
Paediatric-type diffuse high-grade gliomas in the 5th CNS WHO Classification.
Pathologica
; 114(6): 422-435, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36534421
17.
Upfront treatment with mTOR inhibitor everolimus in pediatric low-grade gliomas: A single-center experience.
Int J Cancer
; 148(10): 2522-2534, 2021 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-33320972
18.
Targeting cancer stem cells in medulloblastoma by inhibiting AMBRA1 dual function in autophagy and STAT3 signalling.
Acta Neuropathol
; 142(3): 537-564, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34302498
19.
PATZ1 fusions define a novel molecularly distinct neuroepithelial tumor entity with a broad histological spectrum.
Acta Neuropathol
; 142(5): 841-857, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34417833
20.
Medulloblastoma and familial adenomatous polyposis: Good prognosis and good quality of life in the long-term?
Pediatr Blood Cancer
; 68(4): e28912, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33459525