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C Antozzi

Showing results (41-50 of 53) with videos related to

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Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.
Journal of the Neurological Sciences|December 1, 1991
Prognosis of myasthenia gravis: a multicenter follow-up study of 844 patientsE Beghi, C Antozzi, A P Batocchi, et al.
Neurology|April 13, 2005
Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotoniaC Antozzi, C Frassoni, A Vincent, et al.
Neurology|May 29, 2001
Epileptic phenotypes associated with mitochondrial disordersL Canafoglia, S Franceschetti, C Antozzi, et al.
Neurology|April 7, 2010
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravisP Cavalcante, M Barberis, M Cannone, et al.
Brain : a Journal of Neurology|February 4, 2005
Pathogenesis, diagnosis and treatment of Rasmussen encephalitis: a European consensus statementC G Bien, T Granata, C Antozzi, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.
Neurology|December 25, 2003
Experience with immunomodulatory treatments in Rasmussen's encephalitisT Granata, L Fusco, G Gobbi, et al.
Journal of the Neurological Sciences|August 20, 2016
Early effect of dalfampridine in patients with MS: A multi-instrumental approach to better investigate responsivenessL Brambilla, D Rossi Sebastiano, D Aquino, et al.
Annals of Neurology|February 1, 1996
Clinical heterogeneity of adhalin deficiencyL Morandi, R Barresi, C Di Blasi, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Journal of Neurology|May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNAC Mariotti, N Savarese, A Suomalainen, et al.
Journal of the Neurological Sciences|December 1, 1991
Prognosis of myasthenia gravis: a multicenter follow-up study of 844 patientsE Beghi, C Antozzi, A P Batocchi, et al.
Neurology|April 13, 2005
Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotoniaC Antozzi, C Frassoni, A Vincent, et al.
Neurology|May 29, 2001
Epileptic phenotypes associated with mitochondrial disordersL Canafoglia, S Franceschetti, C Antozzi, et al.
Neurology|April 7, 2010
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravisP Cavalcante, M Barberis, M Cannone, et al.
Brain : a Journal of Neurology|February 4, 2005
Pathogenesis, diagnosis and treatment of Rasmussen encephalitis: a European consensus statementC G Bien, T Granata, C Antozzi, et al.
Neuromuscular Disorders : NMD|July 19, 2000
Phenotypic manifestations associated with CAG-repeat expansion in the androgen receptor gene in male patients and heterozygous females: a clinical and molecular study of 30 familiesC Mariotti, B Castellotti, D Pareyson, et al.
Neurology|December 25, 2003
Experience with immunomodulatory treatments in Rasmussen's encephalitisT Granata, L Fusco, G Gobbi, et al.
Journal of the Neurological Sciences|August 20, 2016
Early effect of dalfampridine in patients with MS: A multi-instrumental approach to better investigate responsivenessL Brambilla, D Rossi Sebastiano, D Aquino, et al.
Annals of Neurology|February 1, 1996
Clinical heterogeneity of adhalin deficiencyL Morandi, R Barresi, C Di Blasi, et al.
Pageof 6