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Claudio Bruno

Showing results (131-140 of 302) with videos related to

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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 17, 2018
Italian recommendations for diagnosis and management of congenital myasthenic syndromesLorenzo Maggi, Pia Bernasconi, Adele D'Amico, et al.
Biochemical and Biophysical Research Communications|November 14, 2012
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 geneChiara Fiorillo, Giacomo Brisca, Denise Cassandrini, et al.
Neuromuscular Disorders : NMD|February 13, 2017
Corrigendum to "Response to: Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both" [Neuromuscular Disorders 26/8 (2016) 549]Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, et al.
Epilepsy & Behavior : E&B|November 30, 2006
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutationsPasquale Striano, Nicola Specchio, Roberta Biancheri, et al.
Human Mutation|May 18, 2004
Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathyAldobrando Broccolini, Enzo Ricci, Denise Cassandrini, et al.
Human Mutation|June 21, 2006
McArdle disease: the mutation spectrum of PYGM in a large Italian cohortClaudio Bruno, Denise Cassandrini, Andrea Martinuzzi, et al.
Journal of Neurology|May 11, 2024
JEWELFISH: 24-month results from an open-label study in non-treatment-naïve patients with SMA receiving treatment with risdiplamClaudia A Chiriboga, Claudio Bruno, Tina Duong, et al.
Parkinsonism & Related Disorders|December 3, 2014
Swallowing disturbances in Parkinson's disease: a multivariate analysis of contributing factorsEmanuele Cereda, Roberto Cilia, Catherine Klersy, et al.
Clinical Nutrition (Edinburgh, Scotland)|March 21, 2021
Predictive fat mass equations for spinal muscular atrophy type I children: Development and internal validationAndrea Foppiani, Ramona De Amicis, Alessandro Leone, et al.
Acta Neuropathologica Communications|April 13, 2018
Zidovudine ameliorates pathology in the mouse model of Duchenne muscular dystrophy via P2RX7 purinoceptor antagonismRasha Al-Khalidi, Chiara Panicucci, Paul Cox, et al.
Pageof 31

Showing results (131-140 of 302) with videos related to

Sort By:
Pageof 31
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 17, 2018
Italian recommendations for diagnosis and management of congenital myasthenic syndromesLorenzo Maggi, Pia Bernasconi, Adele D'Amico, et al.
Biochemical and Biophysical Research Communications|November 14, 2012
Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 geneChiara Fiorillo, Giacomo Brisca, Denise Cassandrini, et al.
Neuromuscular Disorders : NMD|February 13, 2017
Corrigendum to "Response to: Mitochondrial neuropathy affects peripheral and cranial nerves and is primary or secondary or both" [Neuromuscular Disorders 26/8 (2016) 549]Michelangelo Mancuso, Daniele Orsucci, Corrado Angelini, et al.
Epilepsy & Behavior : E&B|November 30, 2006
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutationsPasquale Striano, Nicola Specchio, Roberta Biancheri, et al.
Human Mutation|May 18, 2004
Novel GNE mutations in Italian families with autosomal recessive hereditary inclusion-body myopathyAldobrando Broccolini, Enzo Ricci, Denise Cassandrini, et al.
Human Mutation|June 21, 2006
McArdle disease: the mutation spectrum of PYGM in a large Italian cohortClaudio Bruno, Denise Cassandrini, Andrea Martinuzzi, et al.
Journal of Neurology|May 11, 2024
JEWELFISH: 24-month results from an open-label study in non-treatment-naïve patients with SMA receiving treatment with risdiplamClaudia A Chiriboga, Claudio Bruno, Tina Duong, et al.
Parkinsonism & Related Disorders|December 3, 2014
Swallowing disturbances in Parkinson's disease: a multivariate analysis of contributing factorsEmanuele Cereda, Roberto Cilia, Catherine Klersy, et al.
Clinical Nutrition (Edinburgh, Scotland)|March 21, 2021
Predictive fat mass equations for spinal muscular atrophy type I children: Development and internal validationAndrea Foppiani, Ramona De Amicis, Alessandro Leone, et al.
Acta Neuropathologica Communications|April 13, 2018
Zidovudine ameliorates pathology in the mouse model of Duchenne muscular dystrophy via P2RX7 purinoceptor antagonismRasha Al-Khalidi, Chiara Panicucci, Paul Cox, et al.
Pageof 31