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A Uncini

Showing results (101-110 of 117) with videos related to

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American Journal of Medical Genetics|January 2, 1995
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disordersA Ferlini, M C Patrosso, D Guidetti, et al.
Acta Neurologica Scandinavica|September 1, 1991
HTLV-1-associated myeloneuropathy in an ItalianA Lugaresi, A Uncini, A M Porrini, et al.
Neuroradiology|July 6, 2017
Spinal cord microstructure integrating phase-sensitive inversion recovery and diffusional kurtosis imagingV Panara, R Navarra, P A Mattei, et al.
International Journal of Immunopathology and Pharmacology|April 19, 2011
CD1A and CD1E gene polymorphisms are associated with susceptibility to multiple sclerosisC M Caporale, F Notturno, M Pace, et al.
Annals of Neurology|September 1, 1990
IgM deposits at nodes of Ranvier in a patient with amyotrophic lateral sclerosis, anti-GM1 antibodies, and multifocal motor conduction blockM Santoro, F P Thomas, M E Fink, et al.
European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.
Muscle & Nerve|June 1, 1995
Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplicationA Uncini, G Di Guglielmo, A Di Muzio, et al.
Muscle & Nerve|June 1, 1994
Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a nameA Uncini, S Servidei, G Silvestri, et al.
Thrombosis and Haemostasis|May 11, 1999
Haemostatic abnormalities, cardiac involvement and serum tumor necrosis factor levels in X-linked dystrophic patientsE Porreca, M D Guglielmi, A Uncini, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 7, 2004
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutationM Capasso, A Di Muzio, M Ferrarini, et al.
Pageof 12

Showing results (101-110 of 117) with videos related to

Sort By:
Pageof 12
American Journal of Medical Genetics|January 2, 1995
Androgen receptor gene (CAG)n repeat analysis in the differential diagnosis between Kennedy disease and other motoneuron disordersA Ferlini, M C Patrosso, D Guidetti, et al.
Acta Neurologica Scandinavica|September 1, 1991
HTLV-1-associated myeloneuropathy in an ItalianA Lugaresi, A Uncini, A M Porrini, et al.
Neuroradiology|July 6, 2017
Spinal cord microstructure integrating phase-sensitive inversion recovery and diffusional kurtosis imagingV Panara, R Navarra, P A Mattei, et al.
International Journal of Immunopathology and Pharmacology|April 19, 2011
CD1A and CD1E gene polymorphisms are associated with susceptibility to multiple sclerosisC M Caporale, F Notturno, M Pace, et al.
Annals of Neurology|September 1, 1990
IgM deposits at nodes of Ranvier in a patient with amyotrophic lateral sclerosis, anti-GM1 antibodies, and multifocal motor conduction blockM Santoro, F P Thomas, M E Fink, et al.
European Journal of Neurology|November 27, 2019
Antibody- and macrophage-mediated segmental demyelination in chronic inflammatory demyelinating polyneuropathy: clinical, electrophysiological, immunological and pathological correlatesJ-M Vallat, S Mathis, E Vegezzi, et al.
Muscle & Nerve|June 1, 1995
Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplicationA Uncini, G Di Guglielmo, A Di Muzio, et al.
Muscle & Nerve|June 1, 1994
Ophthalmoplegia, demyelinating neuropathy, leukoencephalopathy, myopathy, and gastrointestinal dysfunction with multiple deletions of mitochondrial DNA: a mitochondrial multisystem disorder in search of a nameA Uncini, S Servidei, G Silvestri, et al.
Thrombosis and Haemostasis|May 11, 1999
Haemostatic abnormalities, cardiac involvement and serum tumor necrosis factor levels in X-linked dystrophic patientsE Porreca, M D Guglielmi, A Uncini, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 7, 2004
Inter-nerves and intra-nerve conduction heterogeneity in CMTX with Arg(15)Gln mutationM Capasso, A Di Muzio, M Ferrarini, et al.
Pageof 12