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G Meola

Showing results (91-100 of 142) with videos related to

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Muscle & Nerve|March 1, 1994
Expression of the low-affinity NGF receptor during human muscle development, regeneration, and in tissue cultureP Baron, E Scarpini, G Meola, et al.
Lancet (London, England)|July 25, 1987
Muscle G6PD deficiencyN Bresolin, L Bet, M Moggio, et al.
European Journal of Neurology|February 1, 2005
Proximal myotonic dystrophy mimicking progressive muscular atrophyG Rotondo, V Sansone, R Cardani, et al.
European Journal of Histochemistry : EJH|July 26, 2006
Apoptosis induced by proteasome inhibition in human myoblast culturesJ Sassone, A Ciammola, C Tiloca, et al.
Cytotechnology|February 24, 2012
Response to DNA-damaging agents in cultured cells from patients with X-linked duchenne muscular dystrophy phenotype: male DMD, female DMD, possible carriersL Barsi, G Meola, M Velicogna, et al.
European Journal of Neurology|February 23, 2008
Bimodal administration of entacapone in Parkinson's disease patients improves motor controlL Bet, S R Bareggi, F Pacei, et al.
European Journal of Histochemistry : EJH|January 13, 2015
Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 inductionL V Renna, R Cardani, A Botta, et al.
Journal of the Neurological Sciences|November 1, 1978
Myopathy with paroxysmal myoglobinuria and focal muscle necrosis following enfluorane anaesthesiaM R Caccia, C Cerri, V Gravame, et al.
Basic and Applied Histochemistry|January 1, 1986
Analysis of fibronectin expression during human muscle differentiationG Meola, E Scarpini, M Velicogna, et al.
Basic and Applied Histochemistry|January 1, 1984
Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle culturesG Meola, E Scarpini, L Manfredi, et al.
Pageof 15

Showing results (91-100 of 142) with videos related to

Sort By:
Pageof 15
Muscle & Nerve|March 1, 1994
Expression of the low-affinity NGF receptor during human muscle development, regeneration, and in tissue cultureP Baron, E Scarpini, G Meola, et al.
Lancet (London, England)|July 25, 1987
Muscle G6PD deficiencyN Bresolin, L Bet, M Moggio, et al.
European Journal of Neurology|February 1, 2005
Proximal myotonic dystrophy mimicking progressive muscular atrophyG Rotondo, V Sansone, R Cardani, et al.
European Journal of Histochemistry : EJH|July 26, 2006
Apoptosis induced by proteasome inhibition in human myoblast culturesJ Sassone, A Ciammola, C Tiloca, et al.
Cytotechnology|February 24, 2012
Response to DNA-damaging agents in cultured cells from patients with X-linked duchenne muscular dystrophy phenotype: male DMD, female DMD, possible carriersL Barsi, G Meola, M Velicogna, et al.
European Journal of Neurology|February 23, 2008
Bimodal administration of entacapone in Parkinson's disease patients improves motor controlL Bet, S R Bareggi, F Pacei, et al.
European Journal of Histochemistry : EJH|January 13, 2015
Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 inductionL V Renna, R Cardani, A Botta, et al.
Journal of the Neurological Sciences|November 1, 1978
Myopathy with paroxysmal myoglobinuria and focal muscle necrosis following enfluorane anaesthesiaM R Caccia, C Cerri, V Gravame, et al.
Basic and Applied Histochemistry|January 1, 1986
Analysis of fibronectin expression during human muscle differentiationG Meola, E Scarpini, M Velicogna, et al.
Basic and Applied Histochemistry|January 1, 1984
Infantile-acute acid maltase deficiency (Pompe's disease): studies of muscle culturesG Meola, E Scarpini, L Manfredi, et al.
Pageof 15