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Electromyography and Clinical Neurophysiology|March 1, 1989
Trigemino-cervical reflex in pathology of the brain stem and of the first cervical cord segmentsB Rossi, S L Pasca, F Sartucci, et al.Current Medicinal Chemistry|August 10, 2011
Targeting mitochondrial dysfunction and neurodegeneration by means of coenzyme Q10 and its analoguesD Orsucci, M Mancuso, E Caldarazzo Ienco, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 19, 2001
Mitochondrial DNA rearrangements in young onset parkinsonism: two case reportsG Siciliano, M Mancuso, R Ceravolo, et al.The Journal of Clinical Endocrinology and Metabolism|November 5, 1997
Clinical and biochemical features of muscle dysfunction in subclinical hypothyroidismF Monzani, N Caraccio, G Siciliano, et al.Case Reports in Neurological Medicine|January 16, 2019
Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY GeneC Simoncini, V Montano, G Alì, et al.Clinical Neurology and Neurosurgery|January 1, 1992
Ocular myopathy without ophthalmoplegia can be a form of mitochondrial myopathyG Siciliano, P Viacava, B Rossi, et al.European Neurology|January 1, 1993
Evoked potentials in the evaluation of patients with mitochondrial myopathyF Sartucci, B Rossi, G Tognoni, et al.Current Molecular Medicine|September 15, 2009
Diagnostic approach to mitochondrial disorders: the need for a reliable biomarkerM Mancuso, D Orsucci, F Coppedè, et al.Mutagenesis|December 19, 2003
Evaluation of cytogenetic and DNA damage in mitochondrial disease patients: effects of coenzyme Q10 therapyL Migliore, S Molinu, A Naccarati, et al.Archives Italiennes De Biologie|July 18, 2017
The proposal of a clinical protocol to assess central and peripheral fatigue in myotonic dystrophy type 1S Baldanzi, G Ricci, M Bottari, et al.Pageof 16