Search research articles
Contact Us
Filters
Showing results (321-330 of 346) with videos related to
Page
of 35
Sort By:
Journal of Alzheimer'S Disease : JAD
|
May 12, 2011
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
Chiara Villa, Laura Ghezzi, Anna M Pietroboni, et al.
Journal of Cellular and Molecular Medicine
|
February 8, 2020
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients
Irene Faravelli, Megi Meneri, Domenica Saccomanno, et al.
Plos One
|
April 17, 2012
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia
Daniela Galimberti, Bernardo Dell'Osso, Chiara Fenoglio, et al.
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
|
December 16, 2010
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease
Eliana Venturelli, Chiara Villa, Chiara Fenoglio, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
February 23, 2012
Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII
Claudio D'Addario, Bernardo Dell'Osso, Maria Carlotta Palazzo, 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.
Plos One
|
April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study
Andrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Journal of Molecular Neuroscience : MN
|
April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients
Daniela Piga, Francesca Magri, Dario Ronchi, et al.
Cellular and Molecular Life Sciences : CMLS
|
November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2A
Federica Rizzo, Silvia Bono, Marc David Ruepp, et al.
Page
of 35
Search research articles
Search
Showing results (321-330 of 346) with videos related to
Sort By:
Page
of 35
Journal of Alzheimer'S Disease : JAD
|
May 12, 2011
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
Chiara Villa, Laura Ghezzi, Anna M Pietroboni, et al.
Journal of Cellular and Molecular Medicine
|
February 8, 2020
Nusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patients
Irene Faravelli, Megi Meneri, Domenica Saccomanno, et al.
Plos One
|
April 17, 2012
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia
Daniela Galimberti, Bernardo Dell'Osso, Chiara Fenoglio, et al.
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
|
December 16, 2010
BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease
Eliana Venturelli, Chiara Villa, Chiara Fenoglio, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
February 23, 2012
Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients with BDI and BDII
Claudio D'Addario, Bernardo Dell'Osso, Maria Carlotta Palazzo, 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.
Plos One
|
April 15, 2016
Clinical and Paraclinical Indicators of Motor System Impairment in Hereditary Spastic Paraplegia: A Pilot Study
Andrea Martinuzzi, Domenico Montanaro, Marinela Vavla, et al.
Journal of Molecular Neuroscience : MN
|
April 24, 2016
New Mutations in NEB Gene Discovered by Targeted Next-Generation Sequencing in Nemaline Myopathy Italian Patients
Daniela Piga, Francesca Magri, Dario Ronchi, et al.
Cellular and Molecular Life Sciences : CMLS
|
November 25, 2023
Combined RNA interference and gene replacement therapy targeting MFN2 as proof of principle for the treatment of Charcot-Marie-Tooth type 2A
Federica Rizzo, Silvia Bono, Marc David Ruepp, et al.
Page
of 35