Lucia Trevisan (L Trevisan)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 6

Top Topics

Chronic Kidney Disease

Mild Cognitive Impairment

Patient Reported Outcomes

Top Venues

British medical bulletin

Molecular genetics & genomic medicine

Clinical case reports

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Lucia Trevisan, A Gaudio, E Monfrini, L Avanzino, A Di Fonzo, P Mandich
Genetics in Parkinson's disease, state-of-the-art and future perspectives. British medical bulletin (2024)
Lucia Trevisan, A Gaudio, E Monfrini, L Avanzino, A Di Fonzo, P Mandich
Genetics in Parkinson's disease, state-of-the-art and future perspectives. British medical bulletin 149 (1) (2024)
Lucia Trevisan, A Gaudio, E Monfrini, L Avanzino, A Di Fonzo, P Mandich
Genetics in Parkinson's disease, state-of-the-art and future perspectives. British medical bulletin 149 (1) (2024)
Federica Ruscitti, Paola Origone, Giulia Rosti, Lucia Trevisan, Roberta Marchese, Andrea Brugnolo, Federico Massa, Paola Castellini, Paola Mandich
A case of Huntington disease-like 2 in a patient of African ancestry: the everlasting support of clinical examination in the molecular era. Clinical case reports 10 (10) (2022)
Federica Ruscitti, Lucia Trevisan, Giulia Rosti, Fabio Gotta, Annalia Cianflone, Alessandro Geroldi, Paola Origone, Anna Pichiecchio, Simona Viglio, Maria Iascone, Paola Mandich
A novel mutation in COL3A1 associates to vascular Ehlers-Danlos syndrome with predominant musculoskeletal involvement. Molecular genetics & genomic medicine 9 (9) (2021)
Fabio Gotta, Merit Lamp, Alessandro Geroldi, Lucia Trevisan, Paola Origone, Giuseppina Fugazza, Sabrina Fabbri, Claudia Nesti, Anna Rubegni, Federica Morani, Filippo Maria Santorelli, Emilia Bellone, Paola Mandich
A novel mutation of Twinkle in Perrault syndrome: A not rare diagnosis? Annals of human genetics 84 (5) (2020)