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European Journal of Neurology|June 21, 2016
Cognition in myotonic dystrophy type 1: a 5-year follow-up studyS Winblad, L Samuelsson, C Lindberg, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 30, 2005
Human skeletal muscle sodium channelopathiesS Vicart, D Sternberg, B Fontaine, et al.Muscle & Nerve|November 1, 1996
Computerized tomography and magnetic resonance muscle imaging in Miyoshi's myopathyG Meola, V Sansone, G Rotondo, et al.Journal of Neurology|June 16, 1978
Muscular carnitine synthesis and palmitate metabolism in vitroG Scarlato, G Meola, E Scarpini, et al.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.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.Critical Reviews in Biotechnology|January 1, 1991
Principles and biotechnological applications of bacterial ice nucleationA Margaritis, A S BassiPageof 54