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Edoardo Monfrini

Showing results (11-20 of 87) with videos related to

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Brain Communications|December 11, 2024
Response to: Are there two disjunct episignatures for KMT2B-related disease?Edoardo Monfrini, Andrea Ciolfi, Marco Ferilli, et al.
International Journal of Molecular Sciences|May 27, 2023
Brain Calcifications: Genetic, Molecular, and Clinical AspectsEdoardo Monfrini, Federica Arienti, Paola Rinchetti, et al.
Parkinsonism & Related Disorders|April 26, 2022
Progressive myoclonus without epilepsy due to a NUS1 frameshift insertion: Dyssynergia cerebellaris myoclonica revisitedEdoardo Monfrini, Claire Miller, Steven J Frucht, et al.
Journal of Parkinson'S Disease|September 27, 2021
A Practical Approach to Early-Onset ParkinsonismGiulietta M Riboldi, Emanuele Frattini, Edoardo Monfrini, et al.
The Lancet. Neurology|September 20, 2024
RAB32 mutation in Parkinson's diseaseEdoardo Monfrini, Raffaella Minardi, Franco Valzania, et al.
Brain : a Journal of Neurology|April 19, 2021
HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystoniaEdoardo Monfrini, Michael Zech, Dora Steel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2022
Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European CohortsMarco Percetti, Edoardo Monfrini, Leonardo Caporali, et al.
Cytogenetic and Genome Research|December 20, 2017
Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1Rosamaria Silipigni, Edoardo Monfrini, Marco Baccarin, et al.
Movement Disorders Clinical Practice|September 28, 2024
Dystonic Tremor as Main Clinical Manifestation of SCA21Vidal Yahya, Claudio Baiata, Edoardo Monfrini, et al.
Frontiers in Neurology|May 16, 2020
Microscopic Polyangiitis With Selective Involvement of Central and Peripheral Nervous System: A Case ReportFederica Arienti, Giulia Franco, Edoardo Monfrini, et al.
Pageof 9

Showing results (11-20 of 87) with videos related to

Sort By:
Pageof 9
Brain Communications|December 11, 2024
Response to: Are there two disjunct episignatures for KMT2B-related disease?Edoardo Monfrini, Andrea Ciolfi, Marco Ferilli, et al.
International Journal of Molecular Sciences|May 27, 2023
Brain Calcifications: Genetic, Molecular, and Clinical AspectsEdoardo Monfrini, Federica Arienti, Paola Rinchetti, et al.
Parkinsonism & Related Disorders|April 26, 2022
Progressive myoclonus without epilepsy due to a NUS1 frameshift insertion: Dyssynergia cerebellaris myoclonica revisitedEdoardo Monfrini, Claire Miller, Steven J Frucht, et al.
Journal of Parkinson'S Disease|September 27, 2021
A Practical Approach to Early-Onset ParkinsonismGiulietta M Riboldi, Emanuele Frattini, Edoardo Monfrini, et al.
The Lancet. Neurology|September 20, 2024
RAB32 mutation in Parkinson's diseaseEdoardo Monfrini, Raffaella Minardi, Franco Valzania, et al.
Brain : a Journal of Neurology|April 19, 2021
HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystoniaEdoardo Monfrini, Michael Zech, Dora Steel, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2022
Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European CohortsMarco Percetti, Edoardo Monfrini, Leonardo Caporali, et al.
Cytogenetic and Genome Research|December 20, 2017
Familial Duplication/Deletion of 1q42.13q43 as Meiotic Consequence of an Intrachromosomal Insertion in Chromosome 1Rosamaria Silipigni, Edoardo Monfrini, Marco Baccarin, et al.
Movement Disorders Clinical Practice|September 28, 2024
Dystonic Tremor as Main Clinical Manifestation of SCA21Vidal Yahya, Claudio Baiata, Edoardo Monfrini, et al.
Frontiers in Neurology|May 16, 2020
Microscopic Polyangiitis With Selective Involvement of Central and Peripheral Nervous System: A Case ReportFederica Arienti, Giulia Franco, Edoardo Monfrini, et al.
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