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Neuroimage. Clinical|October 12, 2022
Clinical relevance of single-subject brain metabolism patterns in amyotrophic lateral sclerosis mutation carriersGiacomo Tondo, Letizia Mazzini, Silvia Paola Caminiti, et al.
Neurorehabilitation and Neural Repair|November 12, 2013
Intensive rehabilitation increases BDNF serum levels in parkinsonian patients: a randomized studyGiuseppe Frazzitta, Roberto Maestri, Maria Felice Ghilardi, et al.
Frontiers in Neurology|January 9, 2019
Multiplex Matrix Metalloproteinases Analysis in the Cerebrospinal Fluid Reveals Potential Specific Patterns in Multiple Sclerosis PatientsMassimiliano Castellazzi, Daniela Ligi, Elena Contaldi, et al.
Journal of the Neurological Sciences|October 31, 2007
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple SclerosisDaniela Galimberti, Diego Scalabrini, Chiara Fenoglio, et al.
Frontiers in Neuroscience|June 29, 2023
A novel GRN mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case reportVeronica Castelnovo, Elisa Canu, Teuta Domi, et al.
Neuroscience Letters|July 26, 2005
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosisDiego Scalabrini, Daniela Galimberti, Chiara Fenoglio, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 17, 2013
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteriaMiryam Carecchio, Monia Magliozzi, Massimiliano Copetti, et al.
Neuroscience Letters|August 31, 2011
Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosisChiara Fenoglio, Claudia Cantoni, Milena De Riz, et al.
Movement Disorders Clinical Practice|April 10, 2024
Comparing Essential Tremor with and without Soft Dystonic Signs and Tremor Combined with Dystonia: The TITAN StudyRoberto Erro, Giulia Lazzeri, Carmen Terranova, et al.
Human Immunology|March 20, 2012
The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas functionElena Boggio, Matteo Melensi, Sara Bocca, et al.
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