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Showing results (21-30 of 28) with videos related to

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The Journal of Headache and Pain|September 1, 2018
New CACNA1A deletions are associated to migraine phenotypesG S Grieco, S Gagliardi, I Ricca, et al.
Biochemical and Biophysical Research Communications|December 25, 2012
Inhibition of the de-myelinating properties of Aicardi-Goutières syndrome lymphocytes by cathepsin D silencingA Pulliero, B Marengo, M Longobardi, et al.
European Journal of Neurology|June 12, 2013
A novel compound heterozygous mutation of C20orf54 gene associated with Brown-Vialetto-Van Laere syndrome in an Italian familyM Bandettini di Poggio, S Gagliardi, M Pardini, et al.
Neurobiology of Aging|January 29, 2010
Peripheral expression of key regulatory kinases in Alzheimer's disease and Parkinson's diseaseM T Armentero, E Sinforiani, C Ghezzi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 27, 2011
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosisR Del Bo, C Tiloca, V Pensato, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 2, 2006
Cooperative study by the Italian neuroendoscopy group on the treatment of 61 colloid cystsP Longatti, U Godano, M Gangemi, et al.
Biology Direct|September 13, 2023
Preliminary insights into RNA in CSF of pediatric SMA patients after 6 months of nusinersenM Garofalo, S Bonanno, S Marcuzzo, et al.
European Journal of Neurology|July 11, 2013
Etiology of first-ever ischaemic stroke in European young adults: the 15 cities young stroke studyN Yesilot Barlas, J Putaala, U Waje-Andreassen, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
The Journal of Headache and Pain|September 1, 2018
New CACNA1A deletions are associated to migraine phenotypesG S Grieco, S Gagliardi, I Ricca, et al.
Biochemical and Biophysical Research Communications|December 25, 2012
Inhibition of the de-myelinating properties of Aicardi-Goutières syndrome lymphocytes by cathepsin D silencingA Pulliero, B Marengo, M Longobardi, et al.
European Journal of Neurology|June 12, 2013
A novel compound heterozygous mutation of C20orf54 gene associated with Brown-Vialetto-Van Laere syndrome in an Italian familyM Bandettini di Poggio, S Gagliardi, M Pardini, et al.
Neurobiology of Aging|January 29, 2010
Peripheral expression of key regulatory kinases in Alzheimer's disease and Parkinson's diseaseM T Armentero, E Sinforiani, C Ghezzi, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 27, 2011
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosisR Del Bo, C Tiloca, V Pensato, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 2, 2006
Cooperative study by the Italian neuroendoscopy group on the treatment of 61 colloid cystsP Longatti, U Godano, M Gangemi, et al.
Biology Direct|September 13, 2023
Preliminary insights into RNA in CSF of pediatric SMA patients after 6 months of nusinersenM Garofalo, S Bonanno, S Marcuzzo, et al.
European Journal of Neurology|July 11, 2013
Etiology of first-ever ischaemic stroke in European young adults: the 15 cities young stroke studyN Yesilot Barlas, J Putaala, U Waje-Andreassen, et al.
Pageof 3