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Andrea Martinuzzi

Showing results (141-150 of 163) with videos related to

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Archives of Neurology|May 10, 2006
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegiaFrancesca Crippa, Chris Panzeri, Andrea Martinuzzi, et al.
Biopreservation and Biobanking|May 23, 2014
Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countriesElena Salvaterra, Roberto Giorda, Maria T Bassi, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Current Oncology (Toronto, Ont.)|September 27, 2024
Internal Consistency and Floor/Ceiling Effects of the Gross Motor Function Measure for Use with Children Affected by Cancer: A Cross-Sectional StudyFrancesca Rossi, Monica Valle, Giovanni Galeoto, et al.
Orphanet Journal of Rare Diseases|July 24, 2023
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participationWalaa Karazi, Renata S Scalco, Mads G Stemmerik, et al.
Human Molecular Genetics|January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein traffickingRobert Behne, Julian Teinert, Miriam Wimmer, et al.
SN Comprehensive Clinical Medicine|September 9, 2020
Avoiding the Banality of Evil in Times of COVID-19: Thinking Differently with a Biopsychosocial Perspective for Future Health and Social Policies DevelopmentMatilde Leonardi, Haejung Lee, Sabina van der Veen, et al.
Brain and Behavior|August 23, 2017
Care pathways models and clinical outcomes in Disorders of consciousnessDavide Sattin, Laura Morganti, Laura De Torres, et al.
Cell Reports|July 20, 2022
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathyAlberto Danese, Simone Patergnani, Alessandra Maresca, et al.
Children (Basel, Switzerland)|September 27, 2025
Development of Functional Abilities Assessment in Paediatric Oncology (FAAP-O) Scale for Children and Adolescents Affected by CancerFrancesca Rossi, Monica Valle, Giulia Carlucci, et al.
Pageof 17

Showing results (141-150 of 163) with videos related to

Sort By:
Pageof 17
Archives of Neurology|May 10, 2006
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegiaFrancesca Crippa, Chris Panzeri, Andrea Martinuzzi, et al.
Biopreservation and Biobanking|May 23, 2014
Pediatric biobanking: a pilot qualitative survey of practices, rules, and researcher opinions in ten European countriesElena Salvaterra, Roberto Giorda, Maria T Bassi, et al.
Orphanet Journal of Rare Diseases|November 25, 2020
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)Renata S Scalco, Alejandro Lucia, Alfredo Santalla, et al.
Current Oncology (Toronto, Ont.)|September 27, 2024
Internal Consistency and Floor/Ceiling Effects of the Gross Motor Function Measure for Use with Children Affected by Cancer: A Cross-Sectional StudyFrancesca Rossi, Monica Valle, Giovanni Galeoto, et al.
Orphanet Journal of Rare Diseases|July 24, 2023
Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participationWalaa Karazi, Renata S Scalco, Mads G Stemmerik, et al.
Human Molecular Genetics|January 10, 2020
Adaptor protein complex 4 deficiency: a paradigm of childhood-onset hereditary spastic paraplegia caused by defective protein traffickingRobert Behne, Julian Teinert, Miriam Wimmer, et al.
SN Comprehensive Clinical Medicine|September 9, 2020
Avoiding the Banality of Evil in Times of COVID-19: Thinking Differently with a Biopsychosocial Perspective for Future Health and Social Policies DevelopmentMatilde Leonardi, Haejung Lee, Sabina van der Veen, et al.
Brain and Behavior|August 23, 2017
Care pathways models and clinical outcomes in Disorders of consciousnessDavide Sattin, Laura Morganti, Laura De Torres, et al.
Cell Reports|July 20, 2022
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathyAlberto Danese, Simone Patergnani, Alessandra Maresca, et al.
Children (Basel, Switzerland)|September 27, 2025
Development of Functional Abilities Assessment in Paediatric Oncology (FAAP-O) Scale for Children and Adolescents Affected by CancerFrancesca Rossi, Monica Valle, Giulia Carlucci, et al.
Pageof 17