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M Sabatelli

Showing results (51-60 of 77) with videos related to

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European Journal of Neurology|September 2, 2014
Nerve ultrasound findings in neuropathy associated with anti-myelin-associated glycoprotein antibodiesM Lucchetta, L Padua, G Granata, et al.
Neurology|July 4, 2008
Natural history of young-adult amyotrophic lateral sclerosisM Sabatelli, F Madia, A Conte, et al.
Journal of the Neurological Sciences|August 16, 2011
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlationA Del Grande, A Conte, S Lattante, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
Journal of the Neurological Sciences|January 7, 2010
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiencyM Luigetti, A Pizzuti, S Bartoletti, et al.
Journal of the Neurological Sciences|September 28, 2010
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotypeM Luigetti, G M Fabrizi, F Madia, 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.
European Journal of Neurology|April 7, 2020
SOD1 p.D12Y variant is associated with amyotrophic lateral sclerosis/distal myopathy spectrumG Tasca, S Lattante, G Marangi, et al.
American Journal of Medical Genetics|February 25, 1998
Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entityM Sabatelli, T Mignogna, G Lippi, et al.
Pageof 8

Showing results (51-60 of 77) with videos related to

Sort By:
Pageof 8
European Journal of Neurology|September 2, 2014
Nerve ultrasound findings in neuropathy associated with anti-myelin-associated glycoprotein antibodiesM Lucchetta, L Padua, G Granata, et al.
Neurology|July 4, 2008
Natural history of young-adult amyotrophic lateral sclerosisM Sabatelli, F Madia, A Conte, et al.
Journal of the Neurological Sciences|August 16, 2011
D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlationA Del Grande, A Conte, S Lattante, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
Journal of the Neurological Sciences|January 7, 2010
Triple A syndrome: a novel compound heterozygous mutation in the AAAS gene in an Italian patient without adrenal insufficiencyM Luigetti, A Pizzuti, S Bartoletti, et al.
Journal of the Neurological Sciences|September 28, 2010
A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotypeM Luigetti, G M Fabrizi, F Madia, 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.
European Journal of Neurology|April 7, 2020
SOD1 p.D12Y variant is associated with amyotrophic lateral sclerosis/distal myopathy spectrumG Tasca, S Lattante, G Marangi, et al.
American Journal of Medical Genetics|February 25, 1998
Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entityM Sabatelli, T Mignogna, G Lippi, et al.
Pageof 8