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Andrea Martinuzzi

Showing results (121-130 of 163) with videos related to

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Clinical Psychology & Psychotherapy|July 18, 2013
Validation of the COURAGE Built Environment Self-Reported QuestionnaireAlberto Raggi, Rui Quintas, Paola Bucciarelli, et al.
Brain : a Journal of Neurology|September 14, 2013
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, et al.
Pediatric Neurology|March 1, 2006
New mutations in TK2 gene associated with mitochondrial DNA depletionSara Galbiati, Andreina Bordoni, Dimitra Papadimitriou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 14, 2020
Safety and efficacy of interferon γ in friedreich's ataxiaMarinela Vavla, Maria Grazia D'Angelo, Filippo Arrigoni, et al.
Human Molecular Genetics|February 19, 2013
The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexesAnna Ghelli, Concetta V Tropeano, Maria Antonietta Calvaruso, et al.
International Journal of Molecular Sciences|February 13, 2025
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome <i>b</i> (<i>MT-CYB</i>) GeneConcetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, et al.
Clinical Psychology & Psychotherapy|July 18, 2013
Mapping SAGE questionnaire to the International Classification of Functioning, Disability and Health (ICF)Alberto Raggi, Rui Quintas, Emanuela Russo, et al.
Human Molecular Genetics|December 24, 2009
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilizationAnna Maria Porcelli, Anna Ghelli, Claudio Ceccarelli, et al.
Human Mutation|January 18, 2008
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegiaAlessia Arnoldi, Alessandra Tonelli, Francesca Crippa, et al.
Neurology|July 19, 2022
Muscle MRI in McArdle Disease: A European Multicenter Observational StudyNicoline Løkken, Karoline Lolk Revsbech, Laura Nørager Jacobsen, et al.
Pageof 17

Showing results (121-130 of 163) with videos related to

Sort By:
Pageof 17
Clinical Psychology & Psychotherapy|July 18, 2013
Validation of the COURAGE Built Environment Self-Reported QuestionnaireAlberto Raggi, Rui Quintas, Paola Bucciarelli, et al.
Brain : a Journal of Neurology|September 14, 2013
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, et al.
Pediatric Neurology|March 1, 2006
New mutations in TK2 gene associated with mitochondrial DNA depletionSara Galbiati, Andreina Bordoni, Dimitra Papadimitriou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 14, 2020
Safety and efficacy of interferon γ in friedreich's ataxiaMarinela Vavla, Maria Grazia D'Angelo, Filippo Arrigoni, et al.
Human Molecular Genetics|February 19, 2013
The cytochrome b p.278Y>C mutation causative of a multisystem disorder enhances superoxide production and alters supramolecular interactions of respiratory chain complexesAnna Ghelli, Concetta V Tropeano, Maria Antonietta Calvaruso, et al.
International Journal of Molecular Sciences|February 13, 2025
Adult Leigh Syndrome Associated with the m.15635T>C Mitochondrial DNA Variant Affecting the Cytochrome <i>b</i> (<i>MT-CYB</i>) GeneConcetta Valentina Tropeano, Chiara La Morgia, Alessandro Achilli, et al.
Clinical Psychology & Psychotherapy|July 18, 2013
Mapping SAGE questionnaire to the International Classification of Functioning, Disability and Health (ICF)Alberto Raggi, Rui Quintas, Emanuela Russo, et al.
Human Molecular Genetics|December 24, 2009
The genetic and metabolic signature of oncocytic transformation implicates HIF1alpha destabilizationAnna Maria Porcelli, Anna Ghelli, Claudio Ceccarelli, et al.
Human Mutation|January 18, 2008
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegiaAlessia Arnoldi, Alessandra Tonelli, Francesca Crippa, et al.
Neurology|July 19, 2022
Muscle MRI in McArdle Disease: A European Multicenter Observational StudyNicoline Løkken, Karoline Lolk Revsbech, Laura Nørager Jacobsen, et al.
Pageof 17