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Alberto Bergareche

Showing results (11-20 of 47) with videos related to

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Frontiers in Neurology|March 25, 2021
A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 GeneAna Vinagre-Aragón, David Campo-Caballero, Elisabet Mondragón-Rezola, et al.
Scientific Reports|July 27, 2022
EMD-based data augmentation method applied to handwriting data for the diagnosis of Essential Tremor using LSTM networksJosé Fernando Adrán Otero, Karmele López-de-Ipina, Oscar Solans Caballer, et al.
Human Genetics|September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystoniaJose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutationsJavier Ruiz-Martínez, Ana Gorostidi, Estibaliz Goyenechea, et al.
ASN Neuro|August 23, 2015
SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential TremorElena Sánchez, Alberto Bergareche, Catharine E Krebs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain)Javier Ruiz-Martínez, Ana Gorostidi, Berta Ibañez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2018
Ratios of proteins in cerebrospinal fluid in Parkinson's disease cognitive decline: prospective studyManuel Delgado-Alvarado, Rosalía Dacosta-Aguayo, Irene Navalpotro-Gómez, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 20, 2013
The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonismJose Felix Martí-Massó, Alberto Bergareche, Vladimir Makarov, et al.
Frontiers in Neurology|June 16, 2022
A Set of Reliable Samples for the Study of Biomarkers for the Early Diagnosis of Parkinson's DiseaseMarcela Konjevod, Jorge Sáiz, Coral Barbas, et al.
Human Molecular Genetics|October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsyAlberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Frontiers in Neurology|March 25, 2021
A More Homogeneous Phenotype in Parkinson's Disease Related to R1441G Mutation in the LRRK2 GeneAna Vinagre-Aragón, David Campo-Caballero, Elisabet Mondragón-Rezola, et al.
Scientific Reports|July 27, 2022
EMD-based data augmentation method applied to handwriting data for the diagnosis of Essential Tremor using LSTM networksJosé Fernando Adrán Otero, Karmele López-de-Ipina, Oscar Solans Caballer, et al.
Human Genetics|September 14, 2011
Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystoniaJose Felix Marti-Masso, Javier Ruiz-Martínez, Vladimir Makarov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 26, 2011
Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutationsJavier Ruiz-Martínez, Ana Gorostidi, Estibaliz Goyenechea, et al.
ASN Neuro|August 23, 2015
SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential TremorElena Sánchez, Alberto Bergareche, Catharine E Krebs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 20, 2010
Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain)Javier Ruiz-Martínez, Ana Gorostidi, Berta Ibañez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2018
Ratios of proteins in cerebrospinal fluid in Parkinson's disease cognitive decline: prospective studyManuel Delgado-Alvarado, Rosalía Dacosta-Aguayo, Irene Navalpotro-Gómez, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 20, 2013
The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonismJose Felix Martí-Massó, Alberto Bergareche, Vladimir Makarov, et al.
Frontiers in Neurology|June 16, 2022
A Set of Reliable Samples for the Study of Biomarkers for the Early Diagnosis of Parkinson's DiseaseMarcela Konjevod, Jorge Sáiz, Coral Barbas, et al.
Human Molecular Genetics|October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsyAlberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
Pageof 5