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Author/Creator Nardella, Marta

1. Age and sex prevalence estimate of Joubert syndrome in Italy. (25th February 2020)

Authors:
Nuovo, Sara; Bacigalupo, Ilaria; Ginevrino, Monia; Battini, Roberta; Bertini, Enrico; Borgatti, Renato; Casella, Antonella; Micalizzi, Alessia; Nardella, Marta; Romaniello, Romina; Serpieri, Valentina; Zanni, Ginevra; Valente, Enza Maria; Vanacore, Nicola
Journal:
Neurology
Issue:
Volume 94:Number 8(2020)
Page Start:
Record Type:
Journal Article
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2. Heterozygous missense variants of SPTBN2 are a frequent cause of congenital cerebellar ataxia. Issue 2 (5th June 2019)

Authors:
Nicita, Francesco; Nardella, Marta; Bellacchio, Emanuele; Alfieri, Paolo; Terrone, Gaetano; Piccini, Giorgia; Graziola, Federica; Pignata, Claudio; Capuano, Alessandro; Bertini, Enrico; Zanni, Ginevra
Journal:
Clinical genetics
Issue:
Volume 96:Issue 2(2019)
Page Start:
169
Record Type:
Journal Article
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3. Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia. (May 2017)

Authors:
Travaglini, Lorena; Nardella, Marta; Bellacchio, Emanuele; D'Amico, Adele; Capuano, Alessandro; Frusciante, Roberto; Di Capua, Matteo; Cusmai, Raffaella; Barresi, Sabina; Morlino, Silvia; Fernández-Fernández, José M.; Trivisano, Marina; Specchio, Nicola; Valeriani, Massimiliano; Vigevano, Federic...
Journal:
European journal of paediatric neurology
Issue:
Volume 21:Number 3(2017:May)
Page Start:
450
Record Type:
Journal Article
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