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Barbara Garavaglia

Showing results (21-30 of 129) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2007
Normal cardiovascular reflex testing in patients with parkin diseaseFrancesca Del Sorbo, Antonio E Elia, Gabriella De Joanna, et al.
Parkinsonism & Related Disorders|January 4, 2016
Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotypeMiryam Carecchio, Celeste Panteghini, Chiara Reale, et al.
European Journal of Medical Genetics|April 6, 2018
Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?Federica Invernizzi, Giovanna Zorzi, Andrea Legati, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Frequency of DYT1 mutation in early onset primary dystonia in Italian patientsGiovanna Zorzi, Barbara Garavaglia, Federica Invernizzi, et al.
Frontiers in Genetics|December 6, 2014
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFederica Invernizzi, Anna Ardissone, Eleonora Lamantea, et al.
Frontiers in Genetics|December 25, 2018
Clinical and Biochemical Features in a Patient With <i>Mitochondrial Fission Factor</i> Gene AlterationAlessia Nasca, Francesca Nardecchia, Anna Commone, et al.
Neurobiology of Disease|April 4, 2015
Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patientsPaolo Santambrogio, Sabrina Dusi, Michela Guaraldo, et al.
Brain & Development|October 18, 2011
Early-onset neurodegeneration with brain iron accumulation due to PANK2 mutationDaniela Rossi, Elisa De Grandis, Chiara Barzaghi, et al.
Radiology|June 30, 2009
Age-related iron deposition in the basal ganglia: quantitative analysis in healthy subjectsDomenico Aquino, Alberto Bizzi, Marina Grisoli, et al.
JIMD Reports|March 17, 2015
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of LiteratureAnna Ardissone, Tiziana Granata, Andrea Legati, et al.
Pageof 13

Showing results (21-30 of 129) with videos related to

Sort By:
Pageof 13
Movement Disorders : Official Journal of the Movement Disorder Society|January 19, 2007
Normal cardiovascular reflex testing in patients with parkin diseaseFrancesca Del Sorbo, Antonio E Elia, Gabriella De Joanna, et al.
Parkinsonism & Related Disorders|January 4, 2016
Novel GNAL mutation with intra-familial clinical heterogeneity: Expanding the phenotypeMiryam Carecchio, Celeste Panteghini, Chiara Reale, et al.
European Journal of Medical Genetics|April 6, 2018
Benign hereditary chorea and deletions outside NKX2-1: What's the role of MBIP?Federica Invernizzi, Giovanna Zorzi, Andrea Legati, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2002
Frequency of DYT1 mutation in early onset primary dystonia in Italian patientsGiovanna Zorzi, Barbara Garavaglia, Federica Invernizzi, et al.
Frontiers in Genetics|December 6, 2014
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutationsFederica Invernizzi, Anna Ardissone, Eleonora Lamantea, et al.
Frontiers in Genetics|December 25, 2018
Clinical and Biochemical Features in a Patient With <i>Mitochondrial Fission Factor</i> Gene AlterationAlessia Nasca, Francesca Nardecchia, Anna Commone, et al.
Neurobiology of Disease|April 4, 2015
Mitochondrial iron and energetic dysfunction distinguish fibroblasts and induced neurons from pantothenate kinase-associated neurodegeneration patientsPaolo Santambrogio, Sabrina Dusi, Michela Guaraldo, et al.
Brain & Development|October 18, 2011
Early-onset neurodegeneration with brain iron accumulation due to PANK2 mutationDaniela Rossi, Elisa De Grandis, Chiara Barzaghi, et al.
Radiology|June 30, 2009
Age-related iron deposition in the basal ganglia: quantitative analysis in healthy subjectsDomenico Aquino, Alberto Bizzi, Marina Grisoli, et al.
JIMD Reports|March 17, 2015
Mitochondrial Complex III Deficiency Caused by TTC19 Defects: Report of a Novel Mutation and Review of LiteratureAnna Ardissone, Tiziana Granata, Andrea Legati, et al.
Pageof 13