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G Tomelleri

Showing results (51-60 of 60) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2009
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1CM Filosto, P Tonin, G Vattemi, et al.
Lancet (London, England)|June 8, 1996
Critical illness myopathy and neuropathyN Latronico, F Fenzi, D Recupero, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathyG Vattemi, M Neri, S Piffer, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patientsG Novelli, M Gennarelli, E Menegazzo, et al.
Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2007
Comparative analysis of visual and semi-quantitative assessment of striatal [123I]FP-CIT-SPET binding in Parkinson's diseaseS Ottaviani, M Tinazzi, I Pasquin, et al.
Clinical Neuropathology|February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsyP Bazzi, M Moggio, A Prelle, et al.
Neuromuscular Disorders : NMD|May 3, 2016
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathyV Guglielmi, A Oosterhof, N C Voermans, et al.
Italian Journal of Neurological Sciences|August 1, 1996
Familial cavernous hemangioma with atypical neuroimagingM G Passarin, A Salviati, G Gambina, et al.
European Journal of Neurology|February 18, 2017
Screening for Fabry disease in patients with ischaemic stroke at young age: the Italian Project on Stroke in Young AdultsL Poli, M Zedde, A Zini, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2009
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1CM Filosto, P Tonin, G Vattemi, et al.
Lancet (London, England)|June 8, 1996
Critical illness myopathy and neuropathyN Latronico, F Fenzi, D Recupero, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathyG Vattemi, M Neri, S Piffer, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patientsG Novelli, M Gennarelli, E Menegazzo, et al.
Brain Pathology (Zurich, Switzerland)|April 17, 2001
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophyG Zanusso, G Vattemi, S Ferrari, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 6, 2007
Comparative analysis of visual and semi-quantitative assessment of striatal [123I]FP-CIT-SPET binding in Parkinson's diseaseS Ottaviani, M Tinazzi, I Pasquin, et al.
Clinical Neuropathology|February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsyP Bazzi, M Moggio, A Prelle, et al.
Neuromuscular Disorders : NMD|May 3, 2016
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathyV Guglielmi, A Oosterhof, N C Voermans, et al.
Italian Journal of Neurological Sciences|August 1, 1996
Familial cavernous hemangioma with atypical neuroimagingM G Passarin, A Salviati, G Gambina, et al.
European Journal of Neurology|February 18, 2017
Screening for Fabry disease in patients with ischaemic stroke at young age: the Italian Project on Stroke in Young AdultsL Poli, M Zedde, A Zini, et al.
Pageof 6