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Human Molecular Genetics
|
October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy
Alberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
Plos One
|
January 10, 2013
Αlpha-synuclein levels in blood plasma from LRRK2 mutation carriers
Ana Gorostidi, Alberto Bergareche, Javier Ruiz-Martínez, et al.
Plos One
|
June 9, 2017
The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics
Fermin Moreno, Begoña Indakoetxea, Myriam Barandiaran, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 22, 2015
DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2 R1441G Parkinson's disease
Alberto Bergareche, Maria Cruz Rodríguez-Oroz, Ainara Estanga, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 27, 2017
Tau/α-synuclein ratio and inflammatory proteins in Parkinson's disease: An exploratory study
Manuel Delgado-Alvarado, Belén Gago, Ana Gorostidi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 21, 2013
Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2
Javier Ruiz-Martínez, Patricia de la Riva, Maria C Rodríguez-Oroz, et al.
Journal of Neuropathology and Experimental Neurology
|
July 9, 2010
A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration
Ainhoa Alzualde, Begoña Indakoetxea, Isidre Ferrer, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association
|
August 6, 2025
The role of endothelial dysfunction in the age-related poor prognosis of stroke patients undergoing endovascular treatment
Patricia de la Riva, Jon Rodríguez-Antigüedad, Juan Marta-Enguita, 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.
Nitric Oxide : Biology and Chemistry
|
September 6, 2022
Endothelial NO synthase 786T/T polymorphism increases hemorrhagic transformation after endovascular thrombectomy
Patricia de la Riva, Jon Rodríguez-Antigüedad, Virginia Gómez, et al.
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Search research articles
Search
Showing results (21-30 of 43) with videos related to
Sort By:
Page
of 5
Human Molecular Genetics
|
October 3, 2015
SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy
Alberto Bergareche, Marcin Bednarz, Elena Sánchez, et al.
Plos One
|
January 10, 2013
Αlpha-synuclein levels in blood plasma from LRRK2 mutation carriers
Ana Gorostidi, Alberto Bergareche, Javier Ruiz-Martínez, et al.
Plos One
|
June 9, 2017
The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics
Fermin Moreno, Begoña Indakoetxea, Myriam Barandiaran, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 22, 2015
DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2 R1441G Parkinson's disease
Alberto Bergareche, Maria Cruz Rodríguez-Oroz, Ainara Estanga, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 27, 2017
Tau/α-synuclein ratio and inflammatory proteins in Parkinson's disease: An exploratory study
Manuel Delgado-Alvarado, Belén Gago, Ana Gorostidi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 21, 2013
Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2
Javier Ruiz-Martínez, Patricia de la Riva, Maria C Rodríguez-Oroz, et al.
Journal of Neuropathology and Experimental Neurology
|
July 9, 2010
A novel PRNP Y218N mutation in Gerstmann-Sträussler-Scheinker disease with neurofibrillary degeneration
Ainhoa Alzualde, Begoña Indakoetxea, Isidre Ferrer, et al.
Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association
|
August 6, 2025
The role of endothelial dysfunction in the age-related poor prognosis of stroke patients undergoing endovascular treatment
Patricia de la Riva, Jon Rodríguez-Antigüedad, Juan Marta-Enguita, 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.
Nitric Oxide : Biology and Chemistry
|
September 6, 2022
Endothelial NO synthase 786T/T polymorphism increases hemorrhagic transformation after endovascular thrombectomy
Patricia de la Riva, Jon Rodríguez-Antigüedad, Virginia Gómez, et al.
Page
of 5