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BMC Neurology
|
February 26, 2016
COPPADIS-2015 (COhort of Patients with PArkinson's DIsease in Spain, 2015), a global--clinical evaluations, serum biomarkers, genetic studies and neuroimaging--prospective, multicenter, non-interventional, long-term study on Parkinson's disease progression
Diego Santos-García, Pablo Mir, Esther Cubo, et al.
Journal of Neurology
|
October 23, 2019
POLR3A-related spastic ataxia: new mutations and a look into the phenotype
Jon Infante, Karla M Serrano-Cárdenas, Marc Corral-Juan, et al.
Plos One
|
October 21, 2014
Nonmotor symptoms in LRRK2 G2019S associated Parkinson's disease
Carles Gaig, Dolores Vilas, Jon Infante, et al.
Neurology
|
January 18, 2013
Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease
Maria Sierra, Pascual Sánchez-Juan, María Isabel Martínez-Rodríguez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 24, 2018
α-synuclein (SNCA) but not dynamin 3 (DNM3) influences age at onset of leucine-rich repeat kinase 2 (LRRK2) Parkinson's disease in Spain
Rubén Fernández-Santiago, Alicia Garrido, Jon Infante, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 21, 2020
MicroRNA Deregulation in Blood Serum Identifies Multiple System Atrophy Altered Pathways
Alexandra Pérez-Soriano, Paloma Bravo, Marta Soto, et al.
Parkinsonism & Related Disorders
|
December 18, 2022
Analysis of retinal nerve layers in idiopathic, LRRK2-associated Parkinson's disease and unaffected carriers of G2019S mutation
Andrea Cerveró, Antonio Sánchez-Rodríguez, María Rivera-Sánchez, et al.
European Journal of Neurology
|
August 18, 2021
Serial DaT-SPECT imaging in asymptomatic carriers of LRRK2 G2019S mutation: 8 years' follow-up
Antonio Sánchez-Rodríguez, Isabel Martínez-Rodríguez, Pascual Sánchez-Juan, et al.
Annals of Neurology
|
October 1, 2016
Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1
Kristien Peeters, Paulius Palaima, Ana L Pelayo-Negro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 29, 2013
Genetic variability related to serum uric acid concentration and risk of Parkinson's disease
Isabel González-Aramburu, Pascual Sánchez-Juan, Silvia Jesús, et al.
Page
of 15
Search research articles
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Showing results (71-80 of 145) with videos related to
Sort By:
Page
of 15
BMC Neurology
|
February 26, 2016
COPPADIS-2015 (COhort of Patients with PArkinson's DIsease in Spain, 2015), a global--clinical evaluations, serum biomarkers, genetic studies and neuroimaging--prospective, multicenter, non-interventional, long-term study on Parkinson's disease progression
Diego Santos-García, Pablo Mir, Esther Cubo, et al.
Journal of Neurology
|
October 23, 2019
POLR3A-related spastic ataxia: new mutations and a look into the phenotype
Jon Infante, Karla M Serrano-Cárdenas, Marc Corral-Juan, et al.
Plos One
|
October 21, 2014
Nonmotor symptoms in LRRK2 G2019S associated Parkinson's disease
Carles Gaig, Dolores Vilas, Jon Infante, et al.
Neurology
|
January 18, 2013
Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease
Maria Sierra, Pascual Sánchez-Juan, María Isabel Martínez-Rodríguez, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 24, 2018
α-synuclein (SNCA) but not dynamin 3 (DNM3) influences age at onset of leucine-rich repeat kinase 2 (LRRK2) Parkinson's disease in Spain
Rubén Fernández-Santiago, Alicia Garrido, Jon Infante, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
July 21, 2020
MicroRNA Deregulation in Blood Serum Identifies Multiple System Atrophy Altered Pathways
Alexandra Pérez-Soriano, Paloma Bravo, Marta Soto, et al.
Parkinsonism & Related Disorders
|
December 18, 2022
Analysis of retinal nerve layers in idiopathic, LRRK2-associated Parkinson's disease and unaffected carriers of G2019S mutation
Andrea Cerveró, Antonio Sánchez-Rodríguez, María Rivera-Sánchez, et al.
European Journal of Neurology
|
August 18, 2021
Serial DaT-SPECT imaging in asymptomatic carriers of LRRK2 G2019S mutation: 8 years' follow-up
Antonio Sánchez-Rodríguez, Isabel Martínez-Rodríguez, Pascual Sánchez-Juan, et al.
Annals of Neurology
|
October 1, 2016
Charcot-Marie-Tooth disease type 2G redefined by a novel mutation in LRSAM1
Kristien Peeters, Paulius Palaima, Ana L Pelayo-Negro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 29, 2013
Genetic variability related to serum uric acid concentration and risk of Parkinson's disease
Isabel González-Aramburu, Pascual Sánchez-Juan, Silvia Jesús, et al.
Page
of 15