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E Bertini

Showing results (191-200 of 205) with videos related to

Pageof 21
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Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric studyE Mercuri, S Messina, R Battini, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
Neurology|March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patientsS Benedetti, I Menditto, M Degano, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.
Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.
Neuromuscular Disorders : NMD|July 2, 2013
Six minute walk test in type III spinal muscular atrophy: a 12month longitudinal studyE Mazzone, F Bianco, M Main, et al.
Neuromuscular Disorders : NMD|February 5, 2014
Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patientsE Mazzone, R De Sanctis, L Fanelli, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Cerebroretinal microangiopathy with calcifications and cysts (CRMCC)T A Briggs, G M H Abdel-Salam, M Balicki, et al.
Journal of Neurology|July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian NetworkD Orsucci, C Angelini, E Bertini, et al.
Pageof 21

Showing results (191-200 of 205) with videos related to

Sort By:
Pageof 21
Neurology|September 19, 2008
Neurodegeneration associated with genetic defects in phospholipase A(2)A Gregory, S K Westaway, I E Holm, et al.
Neuromuscular Disorders : NMD|January 24, 2006
Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric studyE Mercuri, S Messina, R Battini, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
Neurology|March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patientsS Benedetti, I Menditto, M Degano, et al.
Neurology|September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population studyS Messina, C Bruno, I Moroni, et al.
Neuromuscular Disorders : NMD|June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian studyS Messina, M Mora, E Pegoraro, et al.
Neuromuscular Disorders : NMD|July 2, 2013
Six minute walk test in type III spinal muscular atrophy: a 12month longitudinal studyE Mazzone, F Bianco, M Main, et al.
Neuromuscular Disorders : NMD|February 5, 2014
Hammersmith Functional Motor Scale and Motor Function Measure-20 in non ambulant SMA patientsE Mazzone, R De Sanctis, L Fanelli, et al.
American Journal of Medical Genetics. Part A|December 14, 2007
Cerebroretinal microangiopathy with calcifications and cysts (CRMCC)T A Briggs, G M H Abdel-Salam, M Balicki, et al.
Journal of Neurology|July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian NetworkD Orsucci, C Angelini, E Bertini, et al.
Pageof 21