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Neurological Research
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September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency
Angelica 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 Mice
Genny 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 listening
Fernando Bravo, Ian Cross, Christopher Hopkins, et al.
Revista Da Sociedade Brasileira De Medicina Tropical
|
June 20, 2020
Cell Death by Toxoplasma gondii
Claudio 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 leukomyeloencephalopathy
Marco 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 findings
Andrea 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 Diseases
Chiara 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-Aspartate
Francesca 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 mutation
Monica 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 study
Emanuele Cereda, Roberto Cilia, Margherita Canesi, et al.
Page
of 31
Search research articles
Search
Showing results (31-40 of 302) with videos related to
Sort By:
Page
of 31
Neurological Research
|
September 3, 2010
Genotype-phenotype correlations in a large series of patients with muscle type CPT II deficiency
Angelica 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 Mice
Genny 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 listening
Fernando Bravo, Ian Cross, Christopher Hopkins, et al.
Revista Da Sociedade Brasileira De Medicina Tropical
|
June 20, 2020
Cell Death by Toxoplasma gondii
Claudio 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 leukomyeloencephalopathy
Marco 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 findings
Andrea 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 Diseases
Chiara 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-Aspartate
Francesca 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 mutation
Monica 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 study
Emanuele Cereda, Roberto Cilia, Margherita Canesi, et al.
Page
of 31