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Barbara Garavaglia

Showing results (101-110 of 129) with videos related to

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European Journal of Human Genetics : EJHG|June 26, 2023
Episignature analysis of moderate effects and mosaicsKonrad Oexle, Michael Zech, Lara G Stühn, et al.
European Journal of Human Genetics : EJHG|April 14, 2005
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in ItaliansDaniele Ghezzi, Cecilia Marelli, Alessandro Achilli, et al.
Neurology. Genetics|March 27, 2020
<i>MYORG</i>-related disease is associated with central pontine calcifications and atypical parkinsonismViorica Chelban, Miryam Carecchio, Gillian Rea, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 30, 2025
Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's DiseaseAgata Fant, Sara Trova, Edoardo Monfrini, et al.
Human Mutation|March 12, 2008
PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrumRoberta Marongiu, Alessandro Ferraris, Tàmara Ialongo, et al.
American Journal of Human Genetics|December 24, 2013
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulationSabrina Dusi, Lorella Valletta, Tobias B Haack, et al.
Neurobiology of Aging|July 11, 2016
Mutational analysis of COQ2 in patients with MSA in ItalyDario Ronchi, Ernesto Di Biase, Giulia Franco, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 27, 2018
Mitochondrial dysfunction in fibroblasts of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Andreina Bordoni, et al.
Iscience|September 20, 2019
Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and NeurogenesisMohamed Taha Moutaoufik, Ramy Malty, Shahreen Amin, et al.
Cell Systems|November 13, 2017
A Map of Human Mitochondrial Protein Interactions Linked to Neurodegeneration Reveals New Mechanisms of Redox Homeostasis and NF-κB SignalingRamy H Malty, Hiroyuki Aoki, Ashwani Kumar, et al.
Pageof 13

Showing results (101-110 of 129) with videos related to

Sort By:
Pageof 13
European Journal of Human Genetics : EJHG|June 26, 2023
Episignature analysis of moderate effects and mosaicsKonrad Oexle, Michael Zech, Lara G Stühn, et al.
European Journal of Human Genetics : EJHG|April 14, 2005
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in ItaliansDaniele Ghezzi, Cecilia Marelli, Alessandro Achilli, et al.
Neurology. Genetics|March 27, 2020
<i>MYORG</i>-related disease is associated with central pontine calcifications and atypical parkinsonismViorica Chelban, Miryam Carecchio, Gillian Rea, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 30, 2025
Compound Heterozygous Structural Variants in Cases with Unsolved PRKN-Associated Parkinson's DiseaseAgata Fant, Sara Trova, Edoardo Monfrini, et al.
Human Mutation|March 12, 2008
PINK1 heterozygous rare variants: prevalence, significance and phenotypic spectrumRoberta Marongiu, Alessandro Ferraris, Tàmara Ialongo, et al.
American Journal of Human Genetics|December 24, 2013
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulationSabrina Dusi, Lorella Valletta, Tobias B Haack, et al.
Neurobiology of Aging|July 11, 2016
Mutational analysis of COQ2 in patients with MSA in ItalyDario Ronchi, Ernesto Di Biase, Giulia Franco, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|September 27, 2018
Mitochondrial dysfunction in fibroblasts of Multiple System AtrophyGiacomo Monzio Compagnoni, Giulio Kleiner, Andreina Bordoni, et al.
Iscience|September 20, 2019
Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and NeurogenesisMohamed Taha Moutaoufik, Ramy Malty, Shahreen Amin, et al.
Cell Systems|November 13, 2017
A Map of Human Mitochondrial Protein Interactions Linked to Neurodegeneration Reveals New Mechanisms of Redox Homeostasis and NF-κB SignalingRamy H Malty, Hiroyuki Aoki, Ashwani Kumar, et al.
Pageof 13