Valentina Monti

ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients

Miryam Carecchio, Niccolò E. Mencacci, Alessandro Iodice et al. · Parkinsonism & Related Disorders · 2017 · 88 citations · Full text

Pediatrics, Adcy5-related Movement Disorders, Motor Disorder +7

Mitochondrial dysfunction in Parkinson disease: evidence in mutant PARK2 fibroblasts

Maria Clara Zanellati, Valentina Monti, Chiara Barzaghi et al. · Frontiers in Genetics · 2015 · 70 citations · Full text

DNA methylation analysis by bisulfite next-generation sequencing for early detection of oral squamous cell carcinoma and high-grade squamous intraepithelial lesion from oral brushing

Luca Morandi, Davide Bartolomeo Gissi, Achille Tarsitano et al. · Journal of Cranio-Maxillofacial Surgery · 2015 · 51 citations · Full text

Cancer Research, Oral Brushing, Medicine +13

Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotype

Miryam Carecchio, Celeste Panteghini, Chiara Reale et al. · Parkinsonism & Related Disorders · 2015 · 44 citations

Disease Heterogeneity, Mendelian Disorder, Genetic Disorder +6

Toward the Standardization of Mitochondrial Proteomics: The Italian Mitochondrial Human Proteome Project Initiative

Tiziana Alberio, Luisa Pieroni, Maurizio Ronci et al. · Journal of Proteome Research · 2017 · 31 citations · Full text

Proteomic Technology, Other Organelles, Mitochondrial Proteome +15