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Author/Creator Rubegni, A.

2. Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy. (3rd September 2018)

Authors:
Mancini, C.; Giorgio, E.; Rubegni, A.; Pradotto, L.; Bagnoli, S.; Rubino, E.; Prontera, P.; Cavalieri, S.; Di Gregorio, E.; Ferrero, M.; Pozzi, E.; Riberi, E.; Ferrero, P.; Nigro, P.; Mauro, A.; Zibetti, M.; Tessa, A.; Barghigiani, M.; Antenora, A.; Sirchia, F.
Journal:
European journal of neurology
Issue:
Volume 26:Number 1(2019)
Page Start:
80
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Rare phenotype of ALS4 associated with heterozygous missense mutation c.5842A > G/p.M1948V in helicase domain of SETX gene. Issue 3 (2nd April 2020)

Authors:
Andreini, I.; Moro, F.; Africa, L.M.; Rubegni, A.; Santorelli, F.M.; Scarpini, C.; Sicurelli, F.; Battisti, C.
Journal:
Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:
Volume 21:Issue 3/4(2020)
Page Start:
312
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗