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I Moroni

Showing results (21-30 of 34) with videos related to

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Gait & Posture|April 23, 2011
Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: results from a multitask locomotor protocolM Ferrarin, G Bovi, M Rabuffetti, et al.
Gait & Posture|September 28, 2011
Gait pattern classification in children with Charcot-Marie-Tooth disease type 1AM Ferrarin, G Bovi, M Rabuffetti, et al.
AJNR. American Journal of Neuroradiology|May 17, 2008
Classification of childhood white matter disorders using proton MR spectroscopic imagingA Bizzi, G Castelli, M Bugiani, et al.
Neuromuscular Disorders : NMD|February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagyA Ruggieri, N Ramachandran, P Wang, et al.
Biochimica Et Biophysica Acta|December 4, 2004
Clinical and molecular findings in children with complex I deficiencyM Bugiani, F Invernizzi, S Alberio, et al.
Journal of the Neurological Sciences|May 5, 2012
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain diseaseS Saredi, A Ardissone, A Ruggieri, et al.
Comprehensive Psychiatry|December 6, 2016
Adult Autism Subthreshold Spectrum (AdAS Spectrum): Validation of a questionnaire investigating subthreshold autism spectrumL Dell'Osso, C Gesi, E Massimetti, et al.
Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
Neurology|March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patientsS Benedetti, I Menditto, M Degano, 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.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Gait & Posture|April 23, 2011
Reliability of instrumented movement analysis as outcome measure in Charcot-Marie-Tooth disease: results from a multitask locomotor protocolM Ferrarin, G Bovi, M Rabuffetti, et al.
Gait & Posture|September 28, 2011
Gait pattern classification in children with Charcot-Marie-Tooth disease type 1AM Ferrarin, G Bovi, M Rabuffetti, et al.
AJNR. American Journal of Neuroradiology|May 17, 2008
Classification of childhood white matter disorders using proton MR spectroscopic imagingA Bizzi, G Castelli, M Bugiani, et al.
Neuromuscular Disorders : NMD|February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagyA Ruggieri, N Ramachandran, P Wang, et al.
Biochimica Et Biophysica Acta|December 4, 2004
Clinical and molecular findings in children with complex I deficiencyM Bugiani, F Invernizzi, S Alberio, et al.
Journal of the Neurological Sciences|May 5, 2012
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain diseaseS Saredi, A Ardissone, A Ruggieri, et al.
Comprehensive Psychiatry|December 6, 2016
Adult Autism Subthreshold Spectrum (AdAS Spectrum): Validation of a questionnaire investigating subthreshold autism spectrumL Dell'Osso, C Gesi, E Massimetti, et al.
Neuromuscular Disorders : NMD|June 26, 2012
Respiratory and cardiac function in congenital muscular dystrophies with alpha dystroglycan deficiencyM Pane, S Messina, G Vasco, et al.
Neurology|March 23, 2007
Phenotypic clustering of lamin A/C mutations in neuromuscular patientsS Benedetti, I Menditto, M Degano, 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.
Pageof 4