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F Cornelio

Showing results (61-70 of 123) with videos related to

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Archives of Gerontology and Geriatrics. Supplement|June 23, 2004
Aging and vestibular system: specific tests and role of melatonin in cognitive involvementD Alpini, A Cesarani, F Fraschini, et al.
Clinical Neuropathology|January 1, 1985
Centronuclear myopathy with unusual mitochondrial abnormalitiesN Canal, G C Comi, M Comola, et al.
Revista Clinica Espanola|April 1, 1987
[Epidermal growth factor]M D Merino Muñoz, J Gómez Rodrigo, F Cornelio Hernández, et al.
Human Mutation|October 26, 1999
Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenitaR Brugnoni, S Galantini, P Confalonieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Propriospinal myoclonus with life threatening tonic spasms as paraneoplastic presentation of breast cancerE Salsano, C Ciano, S Romano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1994
A unique case of dystrophinopathyF D Worzak, M Mora, L Morandi, et al.
Brain : a Journal of Neurology|April 5, 2001
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skippingC Di Blasi, Y He, L Morandi, et al.
Italian Journal of Neurological Sciences|December 1, 1982
Functional evaluation of Duchenne muscular dystrophy: proposal for a protocolF Cornelio, F Dworzak, L Morandi, et al.
Journal of Neurology|January 1, 1982
Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathyM Rimoldi, E Bottacchi, L Rossi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2002
Is the CACNA1A gene involved in familial migraine with aura?R Brugnoni, M Leone, A Rigamonti, et al.
Pageof 13

Showing results (61-70 of 123) with videos related to

Sort By:
Pageof 13
Archives of Gerontology and Geriatrics. Supplement|June 23, 2004
Aging and vestibular system: specific tests and role of melatonin in cognitive involvementD Alpini, A Cesarani, F Fraschini, et al.
Clinical Neuropathology|January 1, 1985
Centronuclear myopathy with unusual mitochondrial abnormalitiesN Canal, G C Comi, M Comola, et al.
Revista Clinica Espanola|April 1, 1987
[Epidermal growth factor]M D Merino Muñoz, J Gómez Rodrigo, F Cornelio Hernández, et al.
Human Mutation|October 26, 1999
Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenitaR Brugnoni, S Galantini, P Confalonieri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 18, 2006
Propriospinal myoclonus with life threatening tonic spasms as paraneoplastic presentation of breast cancerE Salsano, C Ciano, S Romano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1994
A unique case of dystrophinopathyF D Worzak, M Mora, L Morandi, et al.
Brain : a Journal of Neurology|April 5, 2001
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skippingC Di Blasi, Y He, L Morandi, et al.
Italian Journal of Neurological Sciences|December 1, 1982
Functional evaluation of Duchenne muscular dystrophy: proposal for a protocolF Cornelio, F Dworzak, L Morandi, et al.
Journal of Neurology|January 1, 1982
Cytochrome-C-oxidase deficiency in muscles of a floppy infant without mitochondrial myopathyM Rimoldi, E Bottacchi, L Rossi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|July 12, 2002
Is the CACNA1A gene involved in familial migraine with aura?R Brugnoni, M Leone, A Rigamonti, et al.
Pageof 13