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Author/Creator Valente, E.M.

1. A clinical diagnostic algorithm for early onset cerebellar ataxia. (September 2019)

Authors:
Brandsma, R.; Verschuuren-Bemelmans, C.C.; Amrom, D.; Barisic, N.; Baxter, P.; Bertini, E.; Blumkin, L.; Brankovic-Sreckovic, V.; Brouwer, O.F.; Bürk, K.; Catsman-Berrevoets, C.E.; Craiu, D.; de Coo, I.F.M.; Gburek, J.; Kennedy, C.; de Koning, T.J.; Kremer, H.P.H.; Kumar, R.; Macaya, A.; Micalizz...
Journal:
European journal of paediatric neurology
Issue:
Volume 23:Number 5(2019:Sep.)
Page Start:
692
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia. Issue 3 (25th May 2016)

Authors:
Torraco, A.; Bianchi, M.; Verrigni, D.; Gelmetti, V.; Riley, L.; Niceta, M.; Martinelli, D.; Montanari, A.; Guo, Y.; Rizza, T.; Diodato, D.; Di Nottia, M.; Lucarelli, B.; Sorrentino, F.; Piemonte, F.; Francisci, S.; Tartaglia, M.; Valente, E.M.; Dionisi‐Vici, C.; Christodoulou, J.
Journal:
Clinical genetics
Issue:
Volume 91:Issue 3(2017)
Page Start:
441
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Ataxia rating scales are age‐dependent in healthy children. (7th January 2014)

Authors:
Brandsma, Rick; Spits, Anne H; Kuiper, Marieke J; Lunsing, Roelinka J; Burger, Huibert; Kremer, Hubertus P; Sival, Deborah A; Barisic, N.; Baxter, P.; Brankovic‐Sreckovic, V.; Calabrò, G.E.; Catsman‐Berrevoets, C.; de, IFM; Craiu, D.; Dan, B.; Gburek‐Augustat, J.; Kammoun‐Feki, F.; Kennedy, C.; M...
Journal:
Developmental medicine & child neurology
Issue:
Volume 56:Number 6(2014:Jun.)
Page Start:
556
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗