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Showing results (151-160 of 206) with videos related to

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European Journal of Neurology|January 26, 2007
CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical courseD Galimberti, D Scalabrini, C Fenoglio, et al.
Human Molecular Genetics|November 1, 1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patientG P Comi, E Ciafaloni, H A de Silva, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Nuclear Medicine and Biology|November 17, 2001
Biodistribution studies of 99mTc-labeled myoblasts in a murine model of muscular dystrophyF R Colombo, Y Torrente, R Casati, et al.
Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2008
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patientsR Del Bo, S Ghezzi, S Corti, et al.
Human Mutation|May 18, 2006
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGLS Lucchiari, S Pagliarani, S Salani, et al.
Neurology|April 10, 2003
A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafnessM Crimi, S Galbiati, M P Perini, et al.
Acta Neuropathologica|February 18, 2020
Synaptotagmin 13 is neuroprotective across motor neuron diseasesM Nizzardo, M Taiana, F Rizzo, et al.
Clinical Genetics|January 11, 2011
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutationsA Arnoldi, C Crimella, E Tenderini, et al.
Pageof 21

Showing results (151-160 of 206) with videos related to

Sort By:
Pageof 21
European Journal of Neurology|January 26, 2007
CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical courseD Galimberti, D Scalabrini, C Fenoglio, et al.
Human Molecular Genetics|November 1, 1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patientG P Comi, E Ciafaloni, H A de Silva, et al.
Neuromuscular Disorders : NMD|May 23, 2001
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuriaR Cagliani, G P Comi, L Tancredi, et al.
Nuclear Medicine and Biology|November 17, 2001
Biodistribution studies of 99mTc-labeled myoblasts in a murine model of muscular dystrophyF R Colombo, Y Torrente, R Casati, et al.
Neurology|March 15, 2006
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutationR Del Bo, F Locatelli, S Corti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 19, 2008
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patientsR Del Bo, S Ghezzi, S Corti, et al.
Human Mutation|May 18, 2006
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGLS Lucchiari, S Pagliarani, S Salani, et al.
Neurology|April 10, 2003
A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafnessM Crimi, S Galbiati, M P Perini, et al.
Acta Neuropathologica|February 18, 2020
Synaptotagmin 13 is neuroprotective across motor neuron diseasesM Nizzardo, M Taiana, F Rizzo, et al.
Clinical Genetics|January 11, 2011
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutationsA Arnoldi, C Crimella, E Tenderini, et al.
Pageof 21