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Carlo Minetti

Showing results (21-30 of 190) with videos related to

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Neuromuscular Disorders : NMD|May 29, 2002
Two new mutations in the myophosphorylase gene in Italian patients with McArdle's diseaseClaudio Bruno, Roberta Lanzillo, Claudia Biedi, et al.
Cell Cycle (Georgetown, Tex.)|May 15, 2007
Localized treatment with a novel FDA-approved proteasome inhibitor blocks the degradation of dystrophin and dystrophin-associated proteins in mdx miceGloria Bonuccelli, Federica Sotgia, Franco Capozza, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 1, 2002
Altered aquaporin-4 expression in human muscular dystrophies: a common feature?Antonio Frigeri, Grazia Paola Nicchia, Silvia Repetto, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 27, 2007
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutationRoberta Biancheri, Andrea Rossi, Giannina Alpigiani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Dramatic response to levetiracetam in post-ischaemic Holmes' tremorPasquale Striano, Andrea Elefante, Antonietta Coppola, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Respiratory Medicine|October 4, 2016
Respiratory pattern in a FSHD pediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Muscle & Nerve|March 31, 2004
Motor function-muscle strength relationship in spinal muscular atrophyLuciano Merlini, Enrico Bertini, Carlo Minetti, et al.
Neuropediatrics|December 21, 2012
Magnetic resonance imaging "tigroid pattern" in Alexander diseaseRoberta Biancheri, Andrea Rossi, Isabella Ceccherini, et al.
Respiratory Medicine|April 9, 2017
Respiratory pattern in a FSDH paediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Pageof 19

Showing results (21-30 of 190) with videos related to

Sort By:
Pageof 19
Neuromuscular Disorders : NMD|May 29, 2002
Two new mutations in the myophosphorylase gene in Italian patients with McArdle's diseaseClaudio Bruno, Roberta Lanzillo, Claudia Biedi, et al.
Cell Cycle (Georgetown, Tex.)|May 15, 2007
Localized treatment with a novel FDA-approved proteasome inhibitor blocks the degradation of dystrophin and dystrophin-associated proteins in mdx miceGloria Bonuccelli, Federica Sotgia, Franco Capozza, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|June 1, 2002
Altered aquaporin-4 expression in human muscular dystrophies: a common feature?Antonio Frigeri, Grazia Paola Nicchia, Silvia Repetto, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|January 27, 2007
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutationRoberta Biancheri, Andrea Rossi, Giannina Alpigiani, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 21, 2007
Dramatic response to levetiracetam in post-ischaemic Holmes' tremorPasquale Striano, Andrea Elefante, Antonietta Coppola, et al.
Neuromuscular Disorders : NMD|December 5, 2006
Inherited neuromyotonia: a clinical and genetic study of a familyAntonio Falace, Pasquale Striano, Fiore Manganelli, et al.
Respiratory Medicine|October 4, 2016
Respiratory pattern in a FSHD pediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Muscle & Nerve|March 31, 2004
Motor function-muscle strength relationship in spinal muscular atrophyLuciano Merlini, Enrico Bertini, Carlo Minetti, et al.
Neuropediatrics|December 21, 2012
Magnetic resonance imaging "tigroid pattern" in Alexander diseaseRoberta Biancheri, Andrea Rossi, Isabella Ceccherini, et al.
Respiratory Medicine|April 9, 2017
Respiratory pattern in a FSDH paediatric populationFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Pageof 19