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Journal of Neuroinflammation
|
November 20, 2016
Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
Rakel López de Maturana, Valérie Lang, Amaia Zubiarrain, 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 dystonia
Jose 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 mutations
Javier Ruiz-Martínez, Ana Gorostidi, Estibaliz Goyenechea, et al.
Parkinsonism & Related Disorders
|
April 26, 2011
Genetic variation in α-synuclein kinases (CK-2β and GRK-5) and risk of Parkinson's disease
Inés García-Gorostiaga, María Sierra, Pascual Sánchez-Juan, 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.
ASN Neuro
|
August 23, 2015
SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor
Elena Sánchez, Alberto Bergareche, Catharine E Krebs, 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 study
Manuel 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 parkinsonism
Jose Felix Martí-Massó, Alberto Bergareche, Vladimir Makarov, et al.
Frontiers in Neurology
|
July 3, 2023
Corrigendum: Clinical and genetic analysis of Costa Rican patients with Parkinson's disease
Gabriel Torrealba-Acosta, Eric Yu, Tanya Lobo-Prada, et al.
Frontiers in Neurology
|
August 23, 2021
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease
Gabriel Torrealba-Acosta, Eric Yu, Tanya Lobo-Prada, et al.
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Search research articles
Search
Showing results (11-20 of 43) with videos related to
Sort By:
Page
of 5
Journal of Neuroinflammation
|
November 20, 2016
Mutations in LRRK2 impair NF-κB pathway in iPSC-derived neurons
Rakel López de Maturana, Valérie Lang, Amaia Zubiarrain, 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 dystonia
Jose 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 mutations
Javier Ruiz-Martínez, Ana Gorostidi, Estibaliz Goyenechea, et al.
Parkinsonism & Related Disorders
|
April 26, 2011
Genetic variation in α-synuclein kinases (CK-2β and GRK-5) and risk of Parkinson's disease
Inés García-Gorostiaga, María Sierra, Pascual Sánchez-Juan, 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.
ASN Neuro
|
August 23, 2015
SORT1 Mutation Resulting in Sortilin Deficiency and p75(NTR) Upregulation in a Family With Essential Tremor
Elena Sánchez, Alberto Bergareche, Catharine E Krebs, 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 study
Manuel 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 parkinsonism
Jose Felix Martí-Massó, Alberto Bergareche, Vladimir Makarov, et al.
Frontiers in Neurology
|
July 3, 2023
Corrigendum: Clinical and genetic analysis of Costa Rican patients with Parkinson's disease
Gabriel Torrealba-Acosta, Eric Yu, Tanya Lobo-Prada, et al.
Frontiers in Neurology
|
August 23, 2021
Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease
Gabriel Torrealba-Acosta, Eric Yu, Tanya Lobo-Prada, et al.
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of 5