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Journal of Alzheimer'S Disease : JAD
|
June 29, 2011
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis
Maria Serpente, Chiara Fenoglio, Chiara Villa, et al.
Journal of Alzheimer'S Disease : JAD
|
June 18, 2010
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients
Francesco Lescai, Chiara Pirazzini, Giuseppe D'Agostino, et al.
Journal of Neurology
|
October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation
M Sciacco, A Prelle, G P Comi, et al.
Journal of Alzheimer'S Disease : JAD
|
January 12, 2010
GRN variability contributes to sporadic frontotemporal lobar degeneration
Daniela Galimberti, Chiara Fenoglio, Francesca Cortini, et al.
Brain Connectivity
|
January 31, 2023
European Working Group on SARS-CoV-2: Current Understanding, Unknowns, and Recommendations on the Neurological Complications of COVID-19
Harry Crook, Alfredo Ramirez, Akram Hosseini, et al.
Rejuvenation Research
|
May 10, 2011
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration
Chiara Villa, Chiara Fenoglio, Milena De Riz, et al.
Journal of the Neurological Sciences
|
May 18, 2021
Impact of SARS-CoV-2 infection on acute intracerebral haemorrhage in northern Italy
Davide Sangalli, Filippo Martinelli-Boneschi, Maurizio Versino, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
November 27, 2013
Genetic burden of common variants in progressive and bout-onset multiple sclerosis
Melissa Sorosina, Paola Brambilla, Ferdinando Clarelli, et al.
Frontiers in Genetics
|
January 20, 2022
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population
Ferdinando Clarelli, Nadia Barizzone, Eleonora Mangano, et al.
Journal of Neuroimmunology
|
December 18, 2021
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis
E Mascia, F Clarelli, A Zauli, et al.
Page
of 31
Search research articles
Search
Showing results (251-260 of 310) with videos related to
Sort By:
Page
of 31
Journal of Alzheimer'S Disease : JAD
|
June 29, 2011
Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis
Maria Serpente, Chiara Fenoglio, Chiara Villa, et al.
Journal of Alzheimer'S Disease : JAD
|
June 18, 2010
Failure to replicate an association of rs5984894 SNP in the PCDH11X gene in a collection of 1,222 Alzheimer's disease affected patients
Francesco Lescai, Chiara Pirazzini, Giuseppe D'Agostino, et al.
Journal of Neurology
|
October 13, 2001
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation
M Sciacco, A Prelle, G P Comi, et al.
Journal of Alzheimer'S Disease : JAD
|
January 12, 2010
GRN variability contributes to sporadic frontotemporal lobar degeneration
Daniela Galimberti, Chiara Fenoglio, Francesca Cortini, et al.
Brain Connectivity
|
January 31, 2023
European Working Group on SARS-CoV-2: Current Understanding, Unknowns, and Recommendations on the Neurological Complications of COVID-19
Harry Crook, Alfredo Ramirez, Akram Hosseini, et al.
Rejuvenation Research
|
May 10, 2011
Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration
Chiara Villa, Chiara Fenoglio, Milena De Riz, et al.
Journal of the Neurological Sciences
|
May 18, 2021
Impact of SARS-CoV-2 infection on acute intracerebral haemorrhage in northern Italy
Davide Sangalli, Filippo Martinelli-Boneschi, Maurizio Versino, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
November 27, 2013
Genetic burden of common variants in progressive and bout-onset multiple sclerosis
Melissa Sorosina, Paola Brambilla, Ferdinando Clarelli, et al.
Frontiers in Genetics
|
January 20, 2022
Contribution of Rare and Low-Frequency Variants to Multiple Sclerosis Susceptibility in the Italian Continental Population
Ferdinando Clarelli, Nadia Barizzone, Eleonora Mangano, et al.
Journal of Neuroimmunology
|
December 18, 2021
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis
E Mascia, F Clarelli, A Zauli, et al.
Page
of 31