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Medicine|November 1, 1985
Sensory, motor, and autonomic neuropathy in patients with multiple symmetric lipomatosisG Enzi, C Angelini, P Negrin, et al.
Neurology|July 1, 1976
Carnitine deficiency of skeletal muscle: report of a treated caseC Angelini, S Lücke, F Cantarutti
Muscle & Nerve|May 1, 1980
Abnormal myomuscular junctions and AChE in a congenital neuromuscular diseaseS P Bormioli, S Lücke, C Angelini
Rivista Di Neurologia|September 1, 1980
[Lafora disease complicating myoclonus epilepsy. Report of 3 cases]G Testa, M Armani, D Giaretta, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Myopathological findings in progressive myoclonus epilepsyS Pierobon-Bormioli, C Angelini, M Armani, et al.
Minerva Medica|July 7, 1976
[Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract]G Conte, C Angelini, C Locatelli, et al.
Italian Journal of Neurological Sciences|February 1, 1992
Cognitive and psychiatric evaluation of 40 patients with myotonic dystrophyG Colombo, G I Perini, M V Miotti, et al.
Genetic Epidemiology|January 1, 1987
Genetic epidemiology of myotonic dystrophyM L Mostacciuolo, G Barbujani, M Armani, et al.
Journal of Neurology|January 1, 1984
Carnitine and acyltransferase in experimental neurogenic atrophies: changes with treatmentN Bresolin, L Freddo, V Tegazzin, et al.
The Journal of Nervous and Mental Disease|December 1, 1989
Intellectual impairment and cognitive evoked potentials in myotonic dystrophyG I Perini, G Colombo, M Armani, et al.
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