Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Isabella Moroni

Showing results (1-10 of 159) with videos related to

Pageof 16
Sort By:
Muscle & Nerve|January 27, 2015
Childhood onset of acquired neuromyotonia: association with a ganglioneuromaAnna Ardissone, Giovanna Zorzi, Claudia Ciano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
Congenital myasthenic syndrome: phenotypic variability in patients harbouring p.T159P mutation in <i>CHRNE</i> geneAnna Ardissone, Isabella Moroni, Pia Bernasconi, et al.
The Lancet. Neurology|September 21, 2013
Peripheral neuropathy in mitochondrial disordersDavide Pareyson, Giuseppe Piscosquito, Isabella Moroni, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|March 30, 2023
Nutritional status of children affected by X-linked adrenoleukodystrophyIsabella Moroni, Ramona De Amicis, Anna Ardissone, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 9, 2016
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander diseaseDavide Tonduti, Anna Ardissone, Isabella Ceccherini, et al.
Journal of Neuroengineering and Rehabilitation|July 4, 2013
Changes of gait pattern in children with Charcot-Marie-Tooth disease type 1A: a 18 months follow-up studyMaurizio Ferrarin, Tiziana Lencioni, Marco Rabuffetti, et al.
Molecular Genetics and Metabolism Reports|March 1, 2016
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive <i>SDHB</i> mutation with reduced penetranceAnna Ardissone, Federica Invernizzi, Alessia Nasca, et al.
Frontiers in Neurology|June 18, 2021
Pediatric Paroxysmal Exercise-Induced Neurological Symptoms: Clinical Spectrum and Diagnostic AlgorithmFederica Rachele Danti, Federica Invernizzi, Isabella Moroni, et al.
European Journal of Neurology|April 11, 2023
Phenotyping mitochondrial DNA-related diseases in childhood: A cohort study of 150 patientsAnna Ardissone, Giulia Ferrera, Costanza Lamperti, et al.
Brain & Development|June 2, 2006
Effects of riboflavin in children with complex II deficiencyMarianna Bugiani, Eleonora Lamantea, Federica Invernizzi, et al.
Pageof 16

Showing results (1-10 of 159) with videos related to

Sort By:
Pageof 16
Muscle & Nerve|January 27, 2015
Childhood onset of acquired neuromyotonia: association with a ganglioneuromaAnna Ardissone, Giovanna Zorzi, Claudia Ciano, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 11, 2017
Congenital myasthenic syndrome: phenotypic variability in patients harbouring p.T159P mutation in <i>CHRNE</i> geneAnna Ardissone, Isabella Moroni, Pia Bernasconi, et al.
The Lancet. Neurology|September 21, 2013
Peripheral neuropathy in mitochondrial disordersDavide Pareyson, Giuseppe Piscosquito, Isabella Moroni, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|March 30, 2023
Nutritional status of children affected by X-linked adrenoleukodystrophyIsabella Moroni, Ramona De Amicis, Anna Ardissone, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 9, 2016
Unusual presentations and intrafamilial phenotypic variability in infantile onset Alexander diseaseDavide Tonduti, Anna Ardissone, Isabella Ceccherini, et al.
Journal of Neuroengineering and Rehabilitation|July 4, 2013
Changes of gait pattern in children with Charcot-Marie-Tooth disease type 1A: a 18 months follow-up studyMaurizio Ferrarin, Tiziana Lencioni, Marco Rabuffetti, et al.
Molecular Genetics and Metabolism Reports|March 1, 2016
Mitochondrial leukoencephalopathy and complex II deficiency associated with a recessive <i>SDHB</i> mutation with reduced penetranceAnna Ardissone, Federica Invernizzi, Alessia Nasca, et al.
Frontiers in Neurology|June 18, 2021
Pediatric Paroxysmal Exercise-Induced Neurological Symptoms: Clinical Spectrum and Diagnostic AlgorithmFederica Rachele Danti, Federica Invernizzi, Isabella Moroni, et al.
European Journal of Neurology|April 11, 2023
Phenotyping mitochondrial DNA-related diseases in childhood: A cohort study of 150 patientsAnna Ardissone, Giulia Ferrera, Costanza Lamperti, et al.
Brain & Development|June 2, 2006
Effects of riboflavin in children with complex II deficiencyMarianna Bugiani, Eleonora Lamantea, Federica Invernizzi, et al.
Pageof 16