Detalhe da pesquisa
1.
Identification of an atypical microdeletion generating the RNF135-SUZ12 chimeric gene and causing a position effect in an NF1 patient with overgrowth.
Hum Genet
; 136(10): 1329-1339, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28776093
2.
DNA microarray analysis identifies CKS2 and LEPR as potential markers of meningioma recurrence.
Oncologist
; 16(10): 1440-50, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21948653
3.
Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients.
Genes (Basel)
; 11(6)2020 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32575496
4.
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients.
Genes (Basel)
; 10(11)2019 11 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31694342
5.
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype-Phenotype Correlations in A Large Independent Cohort.
Cancers (Basel)
; 11(12)2019 11 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-31766501
6.
Methylation of O6-methylguanine DNA methyltransferase and loss of heterozygosity on 19q and/or 17p are overlapping features of secondary glioblastomas with prolonged survival.
Clin Cancer Res
; 13(9): 2606-13, 2007 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17473190
7.
126 novel mutations in Italian patients with neurofibromatosis type 1.
Mol Genet Genomic Med
; 3(6): 513-25, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26740943