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Cerebroretinal microangiopathy with calcifications and cysts associated with CTC1 and NDP mutations. [electronic resource] by
- Romaniello, Romina
- Arrigoni, Filippo
- Citterio, Andrea
- Tonelli, Alessandra
- Sforzini, Cinzia
- Rizzari, Carmelo
- Pessina, Marco
- Triulzi, Fabio
- Bassi, Maria Teresa
- Borgatti, Renato
Producer: 20140630
In:
Journal of child neurology vol. 28
Availability: No items available.
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7.
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A novel ATP1A2 gene mutation in familial hemiplegic migraine and epilepsy. [electronic resource] by
- Costa, Cinzia
- Prontera, Paolo
- Sarchielli, Paola
- Tonelli, Alessandra
- Bassi, Maria Teresa
- Cupini, Letizia Maria
- Caproni, Stefano
- Siliquini, Sabrina
- Donti, Emilio
- Calabresi, Paolo
Producer: 20140814
In:
Cephalalgia : an international journal of headache vol. 34
Availability: No items available.
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8.
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A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. [electronic resource] by
- Romaniello, Romina
- Zucca, Claudio
- Tonelli, Alessandra
- Bonato, Sara
- Baschirotto, Cinzia
- Zanotta, Nicoletta
- Epifanio, Roberta
- Righini, Andrea
- Bresolin, Nereo
- Bassi, Maria T
- Borgatti, Renato
Producer: 20150422
In:
Journal of neurology, neurosurgery, and psychiatry vol. 81
Availability: No items available.
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Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene. [electronic resource] by
- Tonelli, Alessandra
- D'Angelo, Maria Grazia
- Salati, Roberto
- Villa, Laura
- Germinasi, Chiara
- Frattini, Tiziano
- Meola, Giovanni
- Turconi, Anna Carla
- Bresolin, Nereo
- Bassi, Maria Teresa
Producer: 20060425
In:
Journal of the neurological sciences vol. 241
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A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function. [electronic resource] by
- Vantaggiato, Chiara
- Redaelli, Francesca
- Falcone, Sestina
- Perrotta, Cristiana
- Tonelli, Alessandra
- Bondioni, Sara
- Morbin, Michela
- Riva, Daria
- Saletti, Veronica
- Bonaglia, Maria C
- Giorda, Roberto
- Bresolin, Nereo
- Clementi, Emilio
- Bassi, Maria Teresa
Producer: 20090923
In:
Human mutation vol. 30
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Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin. [electronic resource] by
- Airoldi, Giovanni
- Guidarelli, Andrea
- Cantoni, Orazio
- Panzeri, Chris
- Vantaggiato, Chiara
- Bonato, Sara
- Grazia D'Angelo, Maria
- Falcone, Sestina
- De Palma, Clara
- Tonelli, Alessandra
- Crimella, Claudia
- Bondioni, Sara
- Bresolin, Nereo
- Clementi, Emilio
- Bassi, Maria Teresa
Producer: 20100322
In:
Neurogenetics vol. 11
Availability: No items available.
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A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia. [electronic resource] by
- Arnoldi, Alessia
- Tonelli, Alessandra
- Crippa, Francesca
- Villani, Gaetano
- Pacelli, Consiglia
- Sironi, Manuela
- Pozzoli, Uberto
- D'Angelo, Maria Grazia
- Meola, Giovanni
- Martinuzzi, Andrea
- Crimella, Claudia
- Redaelli, Francesca
- Panzeri, Chris
- Renieri, Alessandra
- Comi, Giacomo Pietro
- Turconi, Anna Carla
- Bresolin, Nereo
- Bassi, Maria Teresa
Producer: 20080416
In:
Human mutation vol. 29
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Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia. [electronic resource] by
- Crippa, Francesca
- Panzeri, Chris
- Martinuzzi, Andrea
- Arnoldi, Alessia
- Redaelli, Francesca
- Tonelli, Alessandra
- Baschirotto, Cinzia
- Vazza, Giovanni
- Mostacciuolo, Maria Luisa
- Daga, Andrea
- Orso, Genny
- Profice, Paolo
- Trabacca, Antonio
- D'Angelo, Maria Grazia
- Comi, Giacomo Pietro
- Galbiati, Sara
- Lamperti, Costanza
- Bonato, Sara
- Pandolfo, Massimo
- Meola, Giovanni
- Musumeci, Olimpia
- Toscano, Antonio
- Trevisan, Carlo Pietro
- Bresolin, Nereo
- Bassi, Maria Teresa
Producer: 20060628
In:
Archives of neurology vol. 63
Availability: No items available.
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