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G Meola

Showing results (51-60 of 142) with videos related to

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Muscle & Nerve|September 25, 2004
Concurrence of facioscapulohumeral muscular dystrophy and myasthenia gravisV Sansone, D S Saperstein, R J Barohn, et al.
Neuromuscular Disorders : NMD|May 1, 1996
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studiesG Meola, V Sansone, S Radice, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1978
The syndrome of carnitine deficiency: morphological and metabolic correlations in two casesG Scarlato, G Pellegrini, C Cerri, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Pentazocine-blocked myogenesis in human foetal muscle culturesG Meola, E Scarpini, L Manfredi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 27, 2016
Drug resistant focal epilepsy in a patient with myotonic dystrophy type 2: casual or causal association?L Giuliano, V Sofia, R Cardani, et al.
Histochemistry and Cell Biology|June 19, 2012
Nuclear ribonucleoprotein-containing foci increase in size in non-dividing cells from patients with myotonic dystrophy type 2M Giagnacovo, M Malatesta, R Cardani, et al.
Experimental Neurology|December 1, 1978
Physiological and histochemical changes of the extensor digitorum longus and soleus muscles after lateral cordotomy in the albino ratM R Caccia, G Meola, G Brignoli, et al.
European Journal of Histochemistry : EJH|January 1, 1994
Enzymatic activity and morphological differentiation in de novo innervated human muscle culturesG Meola, V Sansone, S Radice, et al.
Italian Journal of Neurological Sciences|March 1, 1980
Type 2 atrophy in a pentazocine addicted patientC Mariani, M G Albizzati, S Boni, et al.
European Journal of Histochemistry : EJH|January 1, 1993
Cytoplasmic restoration and persistence of glucose-6-phosphate dehydrogenase activity in stable hybrid myotubesV Sansone, G Rotondo, G Bottiroli, et al.
Pageof 15

Showing results (51-60 of 142) with videos related to

Sort By:
Pageof 15
Muscle & Nerve|September 25, 2004
Concurrence of facioscapulohumeral muscular dystrophy and myasthenia gravisV Sansone, D S Saperstein, R J Barohn, et al.
Neuromuscular Disorders : NMD|May 1, 1996
A family with an unusual myotonic and myopathic phenotype and no CTG expansion (proximal myotonic myopathy syndrome): a challenge for future molecular studiesG Meola, V Sansone, S Radice, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1978
The syndrome of carnitine deficiency: morphological and metabolic correlations in two casesG Scarlato, G Pellegrini, C Cerri, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Pentazocine-blocked myogenesis in human foetal muscle culturesG Meola, E Scarpini, L Manfredi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 27, 2016
Drug resistant focal epilepsy in a patient with myotonic dystrophy type 2: casual or causal association?L Giuliano, V Sofia, R Cardani, et al.
Histochemistry and Cell Biology|June 19, 2012
Nuclear ribonucleoprotein-containing foci increase in size in non-dividing cells from patients with myotonic dystrophy type 2M Giagnacovo, M Malatesta, R Cardani, et al.
Experimental Neurology|December 1, 1978
Physiological and histochemical changes of the extensor digitorum longus and soleus muscles after lateral cordotomy in the albino ratM R Caccia, G Meola, G Brignoli, et al.
European Journal of Histochemistry : EJH|January 1, 1994
Enzymatic activity and morphological differentiation in de novo innervated human muscle culturesG Meola, V Sansone, S Radice, et al.
Italian Journal of Neurological Sciences|March 1, 1980
Type 2 atrophy in a pentazocine addicted patientC Mariani, M G Albizzati, S Boni, et al.
European Journal of Histochemistry : EJH|January 1, 1993
Cytoplasmic restoration and persistence of glucose-6-phosphate dehydrogenase activity in stable hybrid myotubesV Sansone, G Rotondo, G Bottiroli, et al.
Pageof 15