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Author/Creator Barilaro, A.

1. A novel PAX1 null homozygous mutation in autosomal recessive otofaciocervical syndrome associated with severe combined immunodeficiency. Issue 6 (24th October 2017)

Authors:
Paganini, I.; Sestini, R.; Capone, G.L.; Putignano, A.L.; Contini, E.; Giotti, I.; Gensini, F.; Marozza, A.; Barilaro, A.; Porfirio, B.; Papi, L.
Journal:
Clinical genetics
Issue:
Volume 92:Issue 6(2017)
Page Start:
664
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Safety and efficacy of autologous hematopoietic stem‐cell transplantation following natalizumab discontinuation in aggressive multiple sclerosis. (14th December 2018)

Authors:
Mariottini, A.; Innocenti, C.; Forci, B.; Magnani, E.; Mechi, C.; Barilaro, A.; Nistri, R.; Fani, A.; Saccardi, R.; Massacesi, L.; Repice, A. M.
Journal:
European journal of neurology
Issue:
Volume 26:Number 4(2019)
Page Start:
624
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Subgroup comparison according to clinical phenotype and serostatus in autoimmune encephalitis: a multicenter retrospective study. (14th January 2020)

Authors:
Gastaldi, M.; Mariotto, S.; Giannoccaro, M. P.; Iorio, R.; Zoccarato, M.; Nosadini, M.; Benedetti, L.; Casagrande, S.; Di Filippo, M.; Valeriani, M.; Ricci, S.; Bova, S.; Arbasino, C.; Mauri, M.; Versino, M.; Vigevano, F.; Papetti, L.; Romoli, M.; Lapucci, C.; Massa, F.
Journal:
European journal of neurology
Issue:
Volume 27:Number 4(2020)
Page Start:
633
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗