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Author/Creator Balistreri, Francesca

1. ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy. Issue 1 (21st April 2020)

Authors:
Caporali, Leonardo; Magri, Stefania; Legati, Andrea; Del Dotto, Valentina; Tagliavini, Francesca; Balistreri, Francesca; Nasca, Alessia; La Morgia, Chiara; Carbonelli, Michele; Valentino, Maria L.; Lamantea, Eleonora; Baratta, Silvia; Schöls, Ludger; Schüle, Rebecca; Barboni, Piero; Cascavilla, M...
Journal:
Annals of neurology
Issue:
Volume 88:Issue 1(2020)
Page Start:
18
Record Type:
Journal Article
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2. Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations. Issue 5 (4th May 2021)

Authors:
Abati, Elena; Magri, Stefania; Meneri, Megi; Manenti, Giulia; Velardo, Daniele; Balistreri, Francesca; Pisciotta, Chiara; Saveri, Paola; Bresolin, Nereo; Comi, Giacomo Pietro; Ronchi, Dario; Pareyson, Davide; Taroni, Franco; Corti, Stefania
Journal:
Annals of clinical and translational neurology
Issue:
Volume 8:Issue 5(2021)
Page Start:
1158
Record Type:
Journal Article
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3. DNAJB2‐related Charcot‐Marie‐Tooth disease type 2: Pathomechanism insights and phenotypic spectrum widening. (23rd March 2022)

Authors:
Saveri, Paola; Magri, Stefania; Maderna, Emanuela; Balistreri, Francesca; Lombardi, Raffaella; Ciano, Claudia; Moda, Fabio; Garavaglia, Barbara; Reale, Chiara; Lauria Pinter, Giuseppe; Taroni, Franco; Pareyson, Davide; Pisciotta, Chiara
Journal:
European journal of neurology
Issue:
Volume 29:Number 7(2022)
Page Start:
2056
Record Type:
Journal Article
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