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European Neurology|January 1, 1997
Emerging treatments in myopathiesC Antozzi, P Confalonieri, R Mantegazza, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|May 16, 1984
Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiencyS Di Donato, M Rimoldi, B Garavaglia, et al.Italian Journal of Neurological Sciences|March 1, 1985
Brainstem auditory-evoked responses and clinical picture in a one year follow-up of 18 patients with Friedreich ataxiaG Finocchiaro, A Formenti, F Baiocco, et al.European Journal of Neurology|April 29, 2006
The search for cerebral biomarkers of Huntington's disease: a review of genetic models of age at onset predictionF Squitieri, A Ciarmiello, S Di Donato, et al.Neurology|June 1, 1979
Hepatic ketogenesis and muscle carnitine deficiencyS DiDonato, F Cornelio, G Storchi, et al.Neurology|June 1, 1985
Freeze-fracture analysis of the muscle fiber plasma membrane in Duchenne dystrophyD Peluchetti, M Mora, A Protti, et al.Journal of Neuropathology and Experimental Neurology|May 1, 1997
Transforming growth factor-beta 1 in polymyositis and dermatomyositis correlates with fibrosis but not with mononuclear cell infiltrateP Confalonieri, P Bernasconi, F Cornelio, et al.Journal of Neurology|May 1, 1997
Inflammatory myopathies and systemic disorders: a review of immunopathogenetic mechanisms and clinical featuresR Mantegazza, P Bernasconi, P Confalonieri, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1980
Cherry-red spot myoclonus syndrome and alpha-neuraminidase deficiency: neurophysiological, pharmacological and biochemical study in an adultS Franceschetti, G Uziel, S Di Donato, et al.Journal of Neurology|January 1, 1984
Electromyography and nerve conduction study in autosomal dominant olivopontocerebellar atrophyL Carenini, G Finocchiaro, S Di Donato, et al.Pageof 16