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Chiara Fiorillo

Showing results (21-30 of 142) with videos related to

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The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Journal of Child Neurology|February 20, 2013
Elevated serum creatine kinase and small cerebellum prompt diagnosis of congenital muscular dystrophy due to FKRP mutationsRosanna Trovato, Guja Astrea, Laura Bartalena, et al.
Biochemical and Biophysical Research Communications|July 12, 2011
Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNAAsn geneClaudio Bruno, Denise Cassandrini, Fabiana Fattori, et al.
Dimensions of Critical Care Nursing : DCCN|December 7, 2023
Gas Humidification During Helmet Continuous Positive Airway Pressure: A Crossover Randomized Physiologic Study in Healthy SubjectsLorenzo Ambrosetti, Marco Giani, Emanuele Rezoagli, et al.
Antioxidants (Basel, Switzerland)|November 27, 2024
Muscle Proteome Analysis of Facioscapulohumeral Dystrophy Patients Reveals a Metabolic Rewiring Promoting Oxidative/Reductive Stress Contributing to the Loss of Muscle FunctionManuela Moriggi, Lucia Ruggiero, Enrica Torretta, et al.
International Journal of Cardiology|October 19, 2006
Early detection of biventricular involvement in myotonic dystrophy by tissue DopplerMichele Parisi, Maurizio Galderisi, Milena Sidiropulos, et al.
Italian Journal of Pediatrics|November 17, 2017
Congenital myopathies: clinical phenotypes and new diagnostic toolsDenise Cassandrini, Rosanna Trovato, Anna Rubegni, et al.
Neuropediatrics|January 24, 2023
Recurrent Sensory-Motor Neuropathy Mimicking CIDP as Predominant Presentation of PDH DeficiencyCarolina Croci, Matteo Cataldi, Serena Baratto, et al.
Journal of Child Neurology|January 12, 2013
Novel mutations in TSEN54 in pontocerebellar hypoplasia type 2Roberta Battini, Stefano D'Arrigo, Denise Cassandrini, et al.
Neuromuscular Disorders : NMD|October 13, 2019
'Amish Nemaline Myopathy' in 2 Italian siblings harbouring a novel homozygous mutation in Troponin-I geneAdele D'Amico, Fabiana Fattori, Chiara Fiorillo, et al.
Pageof 15

Showing results (21-30 of 142) with videos related to

Sort By:
Pageof 15
The Journal of International Medical Research|December 7, 2017
Detection of early nocturnal hypoventilation in neuromuscular disordersFederica Trucco, Marina Pedemonte, Chiara Fiorillo, et al.
Journal of Child Neurology|February 20, 2013
Elevated serum creatine kinase and small cerebellum prompt diagnosis of congenital muscular dystrophy due to FKRP mutationsRosanna Trovato, Guja Astrea, Laura Bartalena, et al.
Biochemical and Biophysical Research Communications|July 12, 2011
Mitochondrial myopathy in a child with a muscle-restricted mutation in the mitochondrial transfer RNAAsn geneClaudio Bruno, Denise Cassandrini, Fabiana Fattori, et al.
Dimensions of Critical Care Nursing : DCCN|December 7, 2023
Gas Humidification During Helmet Continuous Positive Airway Pressure: A Crossover Randomized Physiologic Study in Healthy SubjectsLorenzo Ambrosetti, Marco Giani, Emanuele Rezoagli, et al.
Antioxidants (Basel, Switzerland)|November 27, 2024
Muscle Proteome Analysis of Facioscapulohumeral Dystrophy Patients Reveals a Metabolic Rewiring Promoting Oxidative/Reductive Stress Contributing to the Loss of Muscle FunctionManuela Moriggi, Lucia Ruggiero, Enrica Torretta, et al.
International Journal of Cardiology|October 19, 2006
Early detection of biventricular involvement in myotonic dystrophy by tissue DopplerMichele Parisi, Maurizio Galderisi, Milena Sidiropulos, et al.
Italian Journal of Pediatrics|November 17, 2017
Congenital myopathies: clinical phenotypes and new diagnostic toolsDenise Cassandrini, Rosanna Trovato, Anna Rubegni, et al.
Neuropediatrics|January 24, 2023
Recurrent Sensory-Motor Neuropathy Mimicking CIDP as Predominant Presentation of PDH DeficiencyCarolina Croci, Matteo Cataldi, Serena Baratto, et al.
Journal of Child Neurology|January 12, 2013
Novel mutations in TSEN54 in pontocerebellar hypoplasia type 2Roberta Battini, Stefano D'Arrigo, Denise Cassandrini, et al.
Neuromuscular Disorders : NMD|October 13, 2019
'Amish Nemaline Myopathy' in 2 Italian siblings harbouring a novel homozygous mutation in Troponin-I geneAdele D'Amico, Fabiana Fattori, Chiara Fiorillo, et al.
Pageof 15