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Neurology

Showing results (121-130 of 44,188) with videos related to

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Neurology|October 23, 2002
Inherited myoclonus-dystonia: how many causative genes and clinical phenotypes?Yoshiaki Furukawa, Ali H Rajput
Neurology|October 23, 2002
Assessment of low-flow CSF drainage as a treatment for AD: results of a randomized pilot studyG D Silverberg, E Levinthal, E V Sullivan, et al.
Neurology|October 23, 2002
A novel locus for inherited myoclonus-dystonia on 18p11D A Grimes, F Han, A E Lang, et al.
Neurology|October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMAM Mancuso, L Salviati, S Sacconi, et al.
Neurology|October 23, 2002
Acute disseminated encephalomyelitis: a long-term follow-up study of 84 pediatric patientsSilvia Tenembaum, Nestor Chamoles, Natalio Fejerman
Neurology|October 23, 2002
Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndromeV Leuzzi, Ca Carducci, Cl Carducci, et al.
Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.
Neurology|June 17, 1999
Interferon beta-1b treatment modulates TNFalpha and IFNgamma spontaneous gene expression in MSA Gayo, L Mozo, A Suárez, et al.
Neurology|June 17, 1999
Immunoglobulin G Fc-receptor (FcgammaR) IIA and IIIB polymorphisms related to disability in MSK M Myhr, G Raknes, H Nyland, et al.
Neurology|June 17, 1999
Surgical and endovascular treatment of unruptured cerebral aneurysms at university hospitalsS C Johnston, R A Dudley, D R Gress, et al.
Pageof 4,419

Showing results (121-130 of 44,188) with videos related to

Sort By:
Pageof 4,419
Neurology|October 23, 2002
Inherited myoclonus-dystonia: how many causative genes and clinical phenotypes?Yoshiaki Furukawa, Ali H Rajput
Neurology|October 23, 2002
Assessment of low-flow CSF drainage as a treatment for AD: results of a randomized pilot studyG D Silverberg, E Levinthal, E V Sullivan, et al.
Neurology|October 23, 2002
A novel locus for inherited myoclonus-dystonia on 18p11D A Grimes, F Han, A E Lang, et al.
Neurology|October 23, 2002
Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMAM Mancuso, L Salviati, S Sacconi, et al.
Neurology|October 23, 2002
Acute disseminated encephalomyelitis: a long-term follow-up study of 84 pediatric patientsSilvia Tenembaum, Nestor Chamoles, Natalio Fejerman
Neurology|October 23, 2002
Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndromeV Leuzzi, Ca Carducci, Cl Carducci, et al.
Neurology|October 23, 2002
Clinical findings of a myoclonus-dystonia family with two distinct mutationsD Doheny, F Danisi, C Smith, et al.
Neurology|June 17, 1999
Interferon beta-1b treatment modulates TNFalpha and IFNgamma spontaneous gene expression in MSA Gayo, L Mozo, A Suárez, et al.
Neurology|June 17, 1999
Immunoglobulin G Fc-receptor (FcgammaR) IIA and IIIB polymorphisms related to disability in MSK M Myhr, G Raknes, H Nyland, et al.
Neurology|June 17, 1999
Surgical and endovascular treatment of unruptured cerebral aneurysms at university hospitalsS C Johnston, R A Dudley, D R Gress, et al.
Pageof 4,419