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Claudio Bruno

Showing results (31-40 of 302) with videos related to

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Neurological Research|September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiencyAngelica Anichini, Marina Fanin, Christine Vianey-Saban, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|October 24, 2020
Comprehensive Phenotyping of Peripheral Blood T Lymphocytes in Healthy MiceGenny Del Zotto, Elisa Principi, Francesca Antonini, et al.
Human Brain Mapping|September 13, 2019
Anterior cingulate and medial prefrontal cortex response to systematically controlled tonal dissonance during passive music listeningFernando Bravo, Ian Cross, Christopher Hopkins, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|June 20, 2020
Cell Death by Toxoplasma gondiiClaudio Bruno Silva de Oliveira, Isabelle Luna de Oliveira Dantas Berto, Valter Ferreira de Andrade Neto
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 12, 2022
Correction to: Kearns‑Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathyMarco Moscatelli, Anna Ardissone, Eleonora Lamantea, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findingsAndrea Rossi, Roberta Biancheri, Claudio Bruno, et al.
International Journal of Molecular Sciences|August 23, 2020
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle DiseasesChiara Panicucci, Lizzia Raffaghello, Santina Bruzzone, et al.
Journal of Neurochemistry|September 6, 2025
Central Neurophysiological Alterations in Dystrophic mdx Mice Correlate With Reduced Hippocampal Levels of the Endogenous NMDA Receptor Ligand D-AspartateFrancesca Mastrostefano, Martina Garofalo, Tommaso Nuzzo, et al.
BMC Medical Genetics|October 9, 2013
Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutationMonica Bandettini di Poggio, Claudia Nesti, Claudio Bruno, et al.
Journal of Neurology|May 28, 2017
Efficacy of rasagiline and selegiline in Parkinson's disease: a head-to-head 3-year retrospective case-control studyEmanuele Cereda, Roberto Cilia, Margherita Canesi, et al.
Pageof 31

Showing results (31-40 of 302) with videos related to

Sort By:
Pageof 31
Neurological Research|September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiencyAngelica Anichini, Marina Fanin, Christine Vianey-Saban, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|October 24, 2020
Comprehensive Phenotyping of Peripheral Blood T Lymphocytes in Healthy MiceGenny Del Zotto, Elisa Principi, Francesca Antonini, et al.
Human Brain Mapping|September 13, 2019
Anterior cingulate and medial prefrontal cortex response to systematically controlled tonal dissonance during passive music listeningFernando Bravo, Ian Cross, Christopher Hopkins, et al.
Revista Da Sociedade Brasileira De Medicina Tropical|June 20, 2020
Cell Death by Toxoplasma gondiiClaudio Bruno Silva de Oliveira, Isabelle Luna de Oliveira Dantas Berto, Valter Ferreira de Andrade Neto
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 12, 2022
Correction to: Kearns‑Sayre syndrome: expanding spectrum of a "novel" mitochondrial leukomyeloencephalopathyMarco Moscatelli, Anna Ardissone, Eleonora Lamantea, et al.
AJNR. American Journal of Neuroradiology|June 19, 2003
Leigh Syndrome with COX deficiency and SURF1 gene mutations: MR imaging findingsAndrea Rossi, Roberta Biancheri, Claudio Bruno, et al.
International Journal of Molecular Sciences|August 23, 2020
eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle DiseasesChiara Panicucci, Lizzia Raffaghello, Santina Bruzzone, et al.
Journal of Neurochemistry|September 6, 2025
Central Neurophysiological Alterations in Dystrophic mdx Mice Correlate With Reduced Hippocampal Levels of the Endogenous NMDA Receptor Ligand D-AspartateFrancesca Mastrostefano, Martina Garofalo, Tommaso Nuzzo, et al.
BMC Medical Genetics|October 9, 2013
Dopamine-agonist responsive Parkinsonism in a patient with the SANDO syndrome caused by POLG mutationMonica Bandettini di Poggio, Claudia Nesti, Claudio Bruno, et al.
Journal of Neurology|May 28, 2017
Efficacy of rasagiline and selegiline in Parkinson's disease: a head-to-head 3-year retrospective case-control studyEmanuele Cereda, Roberto Cilia, Margherita Canesi, et al.
Pageof 31