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Author/Creator Bassi, Maria T.

2. A novel heterozygous SETX mutation in a patient presenting with chorea and motor neuron disease. Issue 1 (March 2014)

Authors:
Saracchi, Enrico; Castelli, Marianna; Bassi, Maria T.; Brighina, Erika; Cereda, Diletta; Marzorati, Laura; Patassini, Mirko; Appollonio, Ildebrando; Ferrarese, Carlo; Brighina, Laura
Journal:
Amyotrophic lateral sclerosis and frontotemporal degeneration
Issue:
Volume 15:Issue 1/2(2014)
Page Start:
138
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum. (January 2017)

Authors:
Romaniello, Romina; Marelli, Susan; Giorda, Roberto; Bedeschi, Maria F.; Bonaglia, Maria C.; Arrigoni, Filippo; Triulzi, Fabio; Bassi, Maria T.; Borgatti, Renato
Journal:
Journal of child neurology
Issue:
Volume 32:Number 1(2017:Jan.)
Page Start:
60
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗