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G Meola

Showing results (31-40 of 142) with videos related to

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Italian Journal of Neurological Sciences|April 1, 1991
Increased acetylcholine sensitivity in Duchenne muscular dystrophy myotubesG Meola, E Mancinelli, L Geremia, et al.
Journal of Neurology|November 1, 1977
Quantitative EMG and histological carrier detection of Duchenne muscular dystrophyG Scarlato, G Valli, G Meola, et al.
European Journal of Histochemistry : EJH|April 11, 2003
Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathiesG Meola, V Sansone, G Rotondo, et al.
Lancet (London, England)|November 17, 1984
AIDS in an Italian drug addictA Lazzarin, C L Parravicini, G Meola, et al.
Archivio Monaldi Per La Tisiologia E Le Malattie Dell'Apparato Respiratorio|July 1, 1970
[Behavior of blood levels of rifampicin during the course of treatment]V Nitti, F Delli Veneri, A Ninni, et al.
Chemotherapy|January 1, 1972
Rifampicin blood serum levels and half-life during prolonged administration in tuberculous patientsV Nitti, F Delli Veneri, A Ninni, et al.
Theriogenology|July 1, 2004
Hair whorl patterns on the bovine forehead may be related to breeding soundness measuresMelissa G Meola, Temple Grandin, Patrick Burns, et al.
Italian Journal of Neurological Sciences|December 1, 1994
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) familyV Sansone, G Rotondo, L J Ptacek, et al.
Neuromuscular Disorders : NMD|July 26, 2008
A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1R Cardani, E Mancinelli, G Saino, et al.
Minerva Pediatrica|November 15, 1982
[Clinical and histomorphological study of congenital myopathy with minimal lesions]G Meola, E Scarpini, C Minetti, et al.
Pageof 15

Showing results (31-40 of 142) with videos related to

Sort By:
Pageof 15
Italian Journal of Neurological Sciences|April 1, 1991
Increased acetylcholine sensitivity in Duchenne muscular dystrophy myotubesG Meola, E Mancinelli, L Geremia, et al.
Journal of Neurology|November 1, 1977
Quantitative EMG and histological carrier detection of Duchenne muscular dystrophyG Scarlato, G Valli, G Meola, et al.
European Journal of Histochemistry : EJH|April 11, 2003
Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathiesG Meola, V Sansone, G Rotondo, et al.
Lancet (London, England)|November 17, 1984
AIDS in an Italian drug addictA Lazzarin, C L Parravicini, G Meola, et al.
Archivio Monaldi Per La Tisiologia E Le Malattie Dell'Apparato Respiratorio|July 1, 1970
[Behavior of blood levels of rifampicin during the course of treatment]V Nitti, F Delli Veneri, A Ninni, et al.
Chemotherapy|January 1, 1972
Rifampicin blood serum levels and half-life during prolonged administration in tuberculous patientsV Nitti, F Delli Veneri, A Ninni, et al.
Theriogenology|July 1, 2004
Hair whorl patterns on the bovine forehead may be related to breeding soundness measuresMelissa G Meola, Temple Grandin, Patrick Burns, et al.
Italian Journal of Neurological Sciences|December 1, 1994
Mutation in the S4 segment of the adult skeletal sodium channel gene in an Italian paramyotonia congenita (PC) familyV Sansone, G Rotondo, L J Ptacek, et al.
Neuromuscular Disorders : NMD|July 26, 2008
A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1R Cardani, E Mancinelli, G Saino, et al.
Minerva Pediatrica|November 15, 1982
[Clinical and histomorphological study of congenital myopathy with minimal lesions]G Meola, E Scarpini, C Minetti, et al.
Pageof 15