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G Scarlato

Showing results (1-10 of 234) with videos related to

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Rivista Di Istochimica, Normale E Patologica|January 1, 1975
[Contribution of histochemistry to the classification of neuromuscular diseases]G Scarlato
The Medical Journal of Australia|January 22, 1977
Clonazepam in cranial neuralgiasS Smirne, G Scarlato
Recenti Progressi in Medicina|December 1, 1990
[The chronic fatigue syndrome. A multifactorial approach and the treatment possibilities]G Pinardi, G Scarlato
Journal of Neurology|January 1, 1980
A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parentsG Pellegrini, G Scarlato, M Moggio
Acta Neuropathologica. Supplementum|January 1, 1981
Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven casesG Pellegrini, G Scarlato, M Moggio
Journal of Neurology|April 23, 1976
Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophyG Valli, G Scarlato, M Contartese
Journal of Neuropathology and Experimental Neurology|January 1, 1978
Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular diseaseG Scarlato, G Pellegrini, A Veicsteinas
Rivista Di Patologia Nervosa E Mentale|May 1, 1977
[Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]G Scarlato, G Valli, G Meola
Magnetic Resonance in Medicine|December 24, 1997
Energetics of 3.5 s neural activation in humans: a 31P MR spectroscopy studyM Rango, A Castelli, G Scarlato
Acta Neuropathologica. Supplementum|January 1, 1981
Biochemical and morphological studies on a case of systemic carnitine deficiencyC Cerri, G Meola, G Scarlato
Pageof 24

Showing results (1-10 of 234) with videos related to

Sort By:
Pageof 24
Rivista Di Istochimica, Normale E Patologica|January 1, 1975
[Contribution of histochemistry to the classification of neuromuscular diseases]G Scarlato
The Medical Journal of Australia|January 22, 1977
Clonazepam in cranial neuralgiasS Smirne, G Scarlato
Recenti Progressi in Medicina|December 1, 1990
[The chronic fatigue syndrome. A multifactorial approach and the treatment possibilities]G Pinardi, G Scarlato
Journal of Neurology|January 1, 1980
A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parentsG Pellegrini, G Scarlato, M Moggio
Acta Neuropathologica. Supplementum|January 1, 1981
Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven casesG Pellegrini, G Scarlato, M Moggio
Journal of Neurology|April 23, 1976
Quantitative electromyography in the detection of the carriers in Duchenne type muscular dystrophyG Valli, G Scarlato, M Contartese
Journal of Neuropathology and Experimental Neurology|January 1, 1978
Morphologic and metabolic studies in a case of oculo-cranio-somatic neuromuscular diseaseG Scarlato, G Pellegrini, A Veicsteinas
Rivista Di Patologia Nervosa E Mentale|May 1, 1977
[Prevention of duchenne's muscular dystrophy: methodological problems in the detection of carriers (author's transl)]G Scarlato, G Valli, G Meola
Magnetic Resonance in Medicine|December 24, 1997
Energetics of 3.5 s neural activation in humans: a 31P MR spectroscopy studyM Rango, A Castelli, G Scarlato
Acta Neuropathologica. Supplementum|January 1, 1981
Biochemical and morphological studies on a case of systemic carnitine deficiencyC Cerri, G Meola, G Scarlato
Pageof 24