Detalhe da pesquisa
1.
Atypical Molecular Features of Pediatric Tectal Glioma: A Single Institutional Series.
J Pediatr Hematol Oncol
; 45(3): e410-e414, 2023 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36730386
2.
The role of methylation profiling in histologically diagnosed neurocytoma: a case series.
J Neurooncol
; 159(3): 725-733, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35994156
3.
Recurrent TTN metatranscript-only c.39974-11T>G splice variant associated with autosomal recessive arthrogryposis multiplex congenita and myopathy.
Hum Mutat
; 41(2): 403-411, 2020 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-31660661
4.
Nivolumab in the Treatment of Recurrent or Refractory Pediatric Brain Tumors: A Single Institutional Experience.
J Pediatr Hematol Oncol
; 41(4): e235-e241, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30681550
5.
Cooperativity between H3.3K27M and PDGFRA poses multiple therapeutic vulnerabilities in human iPSC-derived diffuse midline glioma avatars.
bioRxiv
; 2023 Feb 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36865329
6.
Circular extrachromosomal DNA promotes tumor heterogeneity in high-risk medulloblastoma.
Nat Genet
; 55(12): 2189-2199, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37945900
7.
Atypical anaplastic astrocytoma with unique molecular features and diffuse leptomeningeal spread in a child with long-term survival.
BMJ Case Rep
; 12(2)2019 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-30765449
8.
Atypical central neurocytoma with novel EWSR1-ATF1 fusion and MUTYH mutation detected by next-generation sequencing.
BMJ Case Rep
; 12(1)2019 Jan 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30642852
9.
Biallelic loss of GNAS in a patient with pediatric medulloblastoma.
Cold Spring Harb Mol Case Stud
; 5(5)2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31624069
10.
Clinical, genetic, and pathologic characterization of FKRP Mexican founder mutation c.1387A>G.
Neurol Genet
; 5(2): e315, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-31041397
11.
Unusual case of occipital lobe dysembryoplastic neuroepithelial tumour with GNAi1-BRAF fusion.
BMJ Case Rep
; 14(1)2021 Jan 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-33504544
12.
Unusual extradural chordoma in an adolescent presenting with lumbar radiculopathy.
BMJ Case Rep
; 13(4)2020 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32265215
13.
Atypical central neurocytoma with aggressive features in a child.
BMJ Case Rep
; 13(6)2020 Jun 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32565441
14.
Low-grade glioneuronal tumour with novel molecular features associated with unusual partial epilepsy in a child.
BMJ Case Rep
; 13(9)2020 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32900747
15.
Rare gain of chromosome 5 in a supratentorial hemispheric paediatric pilomyxoid astrocytoma.
BMJ Case Rep
; 13(3)2020 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32188622
16.
TPM3-NTRK1 fusion in a pleomorphic xanthoastrocytoma presenting with haemorrhage in a child.
BMJ Case Rep
; 13(3)2020 Mar 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32169993
17.
Pituitary tumor apoplexy in adolescents.
World Neurosurg
; 83(4): 644-51, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25527883
18.
Atypical Teratoid Rhabdoid Tumor in a Teenager with Unusual Infiltration Into the Jugular Foramen.
World Neurosurg
; 84(6): 2075.e13-6, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26187115
19.
Characterization of a white bass (Morone chrysops) embryonic cell line with epithelial features.
In Vitro Cell Dev Biol Anim
; 39(1-2): 29-35, 2003.
Artigo
em Inglês
| MEDLINE | ID: mdl-12892524
20.
Unusual high-grade and low-grade glioma in an infant with PPP1CB-ALK gene fusion.
BMJ Case Rep
; 12(2)2019 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30709888