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N Bresolin

Showing results (81-90 of 206) with videos related to

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Clinical Genetics|June 30, 2010
Novel splice-site mutations and a large intragenic deletion in PLA2G6 associated with a severe and rapidly progressive form of infantile neuroaxonal dystrophyA Tonelli, R Romaniello, R Grasso, et al.
Respiratory Physiology & Neurobiology|June 1, 2010
Effects of gender and posture on thoraco-abdominal kinematics during quiet breathing in healthy adultsM Romei, A Lo Mauro, M G D'Angelo, et al.
Brain and Language|April 13, 2007
Evaluation of narrative abilities in patients suffering from Duchenne Muscular DystrophyA Marini, M L Lorusso, M G D'Angelo, et al.
Muscle & Nerve|June 1, 1993
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubesG Meola, J P Tremblay, V Sansone, et al.
Genes and Immunity|August 14, 2009
A population genetics study of the familial Mediterranean fever gene: evidence of balancing selection under an overdominance regimeM Fumagalli, R Cagliani, U Pozzoli, et al.
Perceptual and Motor Skills|June 15, 2007
Language disturbances in a group of participants suffering from Duchenne muscular dystrophy: a pilot studyF Fabbro, A Marini, G Felisari, et al.
Journal of the Neurological Sciences|June 20, 2001
Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscleM Sironi, A Bardoni, G Felisari, et al.
European Neurology|January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult caseT Mongini, C Doriguzzi, L Palmucci, et al.
Neurology|January 13, 2006
Intrathecal chemokine levels in Alzheimer disease and frontotemporal lobar degenerationD Galimberti, N Schoonenboom, P Scheltens, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2001
Intracellular delivery of a Tat-eGFP fusion protein into muscle cellsN J Caron, Y Torrente, G Camirand, et al.
Pageof 21

Showing results (81-90 of 206) with videos related to

Sort By:
Pageof 21
Clinical Genetics|June 30, 2010
Novel splice-site mutations and a large intragenic deletion in PLA2G6 associated with a severe and rapidly progressive form of infantile neuroaxonal dystrophyA Tonelli, R Romaniello, R Grasso, et al.
Respiratory Physiology & Neurobiology|June 1, 2010
Effects of gender and posture on thoraco-abdominal kinematics during quiet breathing in healthy adultsM Romei, A Lo Mauro, M G D'Angelo, et al.
Brain and Language|April 13, 2007
Evaluation of narrative abilities in patients suffering from Duchenne Muscular DystrophyA Marini, M L Lorusso, M G D'Angelo, et al.
Muscle & Nerve|June 1, 1993
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubesG Meola, J P Tremblay, V Sansone, et al.
Genes and Immunity|August 14, 2009
A population genetics study of the familial Mediterranean fever gene: evidence of balancing selection under an overdominance regimeM Fumagalli, R Cagliani, U Pozzoli, et al.
Perceptual and Motor Skills|June 15, 2007
Language disturbances in a group of participants suffering from Duchenne muscular dystrophy: a pilot studyF Fabbro, A Marini, G Felisari, et al.
Journal of the Neurological Sciences|June 20, 2001
Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscleM Sironi, A Bardoni, G Felisari, et al.
European Neurology|January 1, 1992
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult caseT Mongini, C Doriguzzi, L Palmucci, et al.
Neurology|January 13, 2006
Intrathecal chemokine levels in Alzheimer disease and frontotemporal lobar degenerationD Galimberti, N Schoonenboom, P Scheltens, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2001
Intracellular delivery of a Tat-eGFP fusion protein into muscle cellsN J Caron, Y Torrente, G Camirand, et al.
Pageof 21