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S Servidei

Showing results (101-110 of 146) with videos related to

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Neurology|August 26, 2009
Restless legs syndrome with periodic limb movements: a possible cause of idiopathic hyperCKemiaG Della Marca, S Dittoni, M Catteruccia, et al.
Neurology|December 11, 2002
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE geneA Broccolini, M Pescatori, A D'Amico, et al.
Electroencephalography and Clinical Neurophysiology|June 1, 1997
Functional involvement of central nervous system in mitochondrial disordersV Di Lazzaro, D Restuccia, S Servidei, et al.
Neurology|February 19, 2000
GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophyM Mirabella, G Silvestri, G de Rosa, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1993
Myopathy and hypertrophic cardiomyopathy with selective lysis of thick filamentsE Bertini, C Bosman, G Salviati, et al.
Blood|June 20, 1998
Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patientsV De Stefano, P Chiusolo, K Paciaroni, et al.
European Journal of Pediatrics|September 1, 1990
Cardiomyopathy and multicore myopathy with accumulation of intermediate filamentsE Bertini, C Bosman, M Bevilacqua, et al.
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
European Journal of Neurology|May 16, 2012
Muscle MRI in female carriers of dystrophinopathyG Tasca, M Monforte, E Iannaccone, et al.
Muscle & Nerve|May 8, 1998
Functional involvement of cerebral cortex in Duchenne muscular dystrophyV Di Lazzaro, D Restuccia, S Servidei, et al.
Pageof 15

Showing results (101-110 of 146) with videos related to

Sort By:
Pageof 15
Neurology|August 26, 2009
Restless legs syndrome with periodic limb movements: a possible cause of idiopathic hyperCKemiaG Della Marca, S Dittoni, M Catteruccia, et al.
Neurology|December 11, 2002
An Italian family with autosomal recessive inclusion-body myopathy and mutations in the GNE geneA Broccolini, M Pescatori, A D'Amico, et al.
Electroencephalography and Clinical Neurophysiology|June 1, 1997
Functional involvement of central nervous system in mitochondrial disordersV Di Lazzaro, D Restuccia, S Servidei, et al.
Neurology|February 19, 2000
GCG genetic expansions in Italian patients with oculopharyngeal muscular dystrophyM Mirabella, G Silvestri, G de Rosa, et al.
Virchows Archiv. A, Pathological Anatomy and Histopathology|January 1, 1993
Myopathy and hypertrophic cardiomyopathy with selective lysis of thick filamentsE Bertini, C Bosman, G Salviati, et al.
Blood|June 20, 1998
Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patientsV De Stefano, P Chiusolo, K Paciaroni, et al.
European Journal of Pediatrics|September 1, 1990
Cardiomyopathy and multicore myopathy with accumulation of intermediate filamentsE Bertini, C Bosman, M Bevilacqua, et al.
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
European Journal of Neurology|May 16, 2012
Muscle MRI in female carriers of dystrophinopathyG Tasca, M Monforte, E Iannaccone, et al.
Muscle & Nerve|May 8, 1998
Functional involvement of cerebral cortex in Duchenne muscular dystrophyV Di Lazzaro, D Restuccia, S Servidei, et al.
Pageof 15