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Author/Creator Venditti, Martina

1. Co-occurring WARS2 and CHRNA6 mutations in a child with a severe form of infantile parkinsonism. (March 2020)

Authors:
Martinelli, Simone; Cordeddu, Viviana; Galosi, Serena; Lanzo, Ambra; Palma, Eleonora; Pannone, Luca; Ciolfi, Andrea; Di Nottia, Michela; Rizza, Teresa; Bocchinfuso, Gianfranco; Traversa, Alice; Caputo, Viviana; Farrotti, Andrea; Carducci, Claudia; Bernardini, Laura; Cogo, Susanna; Paglione, Maria...
Journal:
Parkinsonism & related disorders
Issue:
Volume 72(2020)
Page Start:
75
Record Type:
Journal Article
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2. Dominantly acting KIF5B variants with pleiotropic cellular consequences cause variable clinical phenotypes. Issue 3 (26th August 2022)

Authors:
Flex, Elisabetta; Albadri, Shahad; Radio, Francesca Clementina; Cecchetti, Serena; Lauri, Antonella; Priolo, Manuela; Kissopoulos, Marta; Carpentieri, Giovanna; Fasano, Giulia; Venditti, Martina; Magliocca, Valentina; Bellacchio, Emanuele; Welch, Carrie L; Colombo, Paolo C; Kochav, Stephanie M; C...
Journal:
Human molecular genetics
Issue:
Volume 32:Issue 3(2023)
Page Start:
473
Record Type:
Journal Article
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3. Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism. (April 2019)

Authors:
Manti, Filippo; Nardecchia, Francesca; Barresi, Sabina; Venditti, Martina; Pizzi, Simone; Hamdan, Fadi F.; Blau, Nenad; Burlina, Alberto; Tartaglia, Marco; Leuzzi, Vincenzo
Journal:
Parkinsonism & related disorders
Issue:
Volume 61(2019)
Page Start:
207
Record Type:
Journal Article
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