TRITTO, VIVIANA

TRITTO, VIVIANA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autori Tipo File Abstract
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort 2023 Paola BettinaglioEleonora ManganoViviana TrittoClaudia CesarettiRoberta BordoniMarco MoscatelliPaola Riva + Article (author) -
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes 2023 Tritto, VivianaCapitanio, DanieleGelfi, CeciliaRiva, Paola Article (author) -
Deregulated expression of polycomb repressive complex 2 target genes in a NF1 patient with microdeletion generating the RNF135-SUZ12 chimeric gene 2023 Viviana TrittoFederico GrilliDonatella MilaniPaola Riva Article (author) -
Expression analysis of NF1-mutated alleles in a rare compound heterozygous spinal NF1 patient by digital PCR 2023 Bettinaglio, PaolaTritto, VivianaRiva, Paola + Article (author) -
New insights into the molecular basis of spinal neurofibromatosis type 1 2023 Bettinaglio, PaolaMangano, EleonoraTritto, VivianaBordoni, RobertaBattaglia, CristinaCesaretti, ClaudiaRiva, Paola + Article (author) -
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes 2022 Tritto, VivianaRusconi, FrancescoRiva, Paola + Article (author) -
Position effect and of modifier Ras pathway genes in Neurofibromatosis type I microdeletion syndrome 2022 V. TrittoC. BattagliaP. Riva + Article (author) -
Preclinical and clinical evidence on the approach-avoidance conflict evaluation as an integrative tool for psychopathology 2022 Rusconi, FForastieri, CTritto, VBattaglioli, E + Article (author) -
Role of hypomorphic variants in variable expressivity of Noonan syndrome 2022 V. TrittoC. BattagliaP. Riva + Article (author) -
NF1 Gene Mutation Mediates Neuronal Signaling De-Regulation Triggering Pediatric Optic Glioma Development: Another Small Step towards a Cure of NF1 Disorder? 2021 P. RivaV. Tritto Article (author) -
Prevalence of NF1 missense mutations and candidate modifier genes in 12 familial and 15 sporadic spinal neurofibromatosis patients 2020 P. RivaV. TrittoC. Battaglia + Article (author) -
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 2019 Tritto, VivianaFerrari, LucaZuccotti, PaolaRiva, Paola + Article (author) -