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Massimo Pandolfo

Showing results (61-70 of 163) with videos related to

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Neurology|April 11, 2014
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutationsChantal Depondt, Simona Donatello, Nicolas Simonis, et al.
Orphanet Journal of Rare Diseases|March 19, 2021
Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological DiseasesAnnemarie E M Post, Thomas Klockgether, G Bernhard Landwehrmeyer, et al.
Epilepsy Research|September 12, 2013
A new locus for familial temporal lobe epilepsy on chromosome 3qLyne Chahine, Bassel Abou-Khalil, Auli Siren, et al.
Human Molecular Genetics|June 30, 2007
Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1Robert Goold, Michael Hubank, Abigail Hunt, et al.
Journal of the Neurological Sciences|March 22, 2017
HLA genotype as a marker of multiple sclerosis prognosis: A pilot studyAndreas P Lysandropoulos, Nicolas Mavroudakis, Massimo Pandolfo, et al.
Plos One|January 26, 2010
Two new pimelic diphenylamide HDAC inhibitors induce sustained frataxin upregulation in cells from Friedreich's ataxia patients and in a mouse modelMyriam Rai, Elisabetta Soragni, C James Chou, et al.
Stem Cells and Development|November 16, 2006
A real-time PCR approach to evaluate adipogenic potential of amniotic fluid-derived human mesenchymal stem cellsPaola De Gemmis, Cristina Lapucci, Matteo Bertelli, et al.
Brain Communications|March 3, 2023
Proprioceptors-enriched neuronal cultures from induced pluripotent stem cells from Friedreich ataxia patients show altered transcriptomic and proteomic profiles, abnormal neurite extension, and impaired electrophysiological propertiesChiara Dionisi, Marine Chazalon, Myriam Rai, et al.
Human Molecular Genetics|February 9, 2017
Friedreich ataxia-induced pluripotent stem cell-derived neurons show a cellular phenotype that is corrected by a benzamide HDAC inhibitorFranca Codazzi, Amelié Hu, Myriam Rai, et al.
Plos One|October 18, 2007
Proprotein convertase subtilisin/kexin type 9 (PCSK9) gene is a risk factor of large-vessel atherosclerosis strokeShérine Abboud, Pekka J Karhunen, Dieter Lütjohann, et al.
Pageof 17

Showing results (61-70 of 163) with videos related to

Sort By:
Pageof 17
Neurology|April 11, 2014
Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutationsChantal Depondt, Simona Donatello, Nicolas Simonis, et al.
Orphanet Journal of Rare Diseases|March 19, 2021
Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological DiseasesAnnemarie E M Post, Thomas Klockgether, G Bernhard Landwehrmeyer, et al.
Epilepsy Research|September 12, 2013
A new locus for familial temporal lobe epilepsy on chromosome 3qLyne Chahine, Bassel Abou-Khalil, Auli Siren, et al.
Human Molecular Genetics|June 30, 2007
Down-regulation of the dopamine receptor D2 in mice lacking ataxin 1Robert Goold, Michael Hubank, Abigail Hunt, et al.
Journal of the Neurological Sciences|March 22, 2017
HLA genotype as a marker of multiple sclerosis prognosis: A pilot studyAndreas P Lysandropoulos, Nicolas Mavroudakis, Massimo Pandolfo, et al.
Plos One|January 26, 2010
Two new pimelic diphenylamide HDAC inhibitors induce sustained frataxin upregulation in cells from Friedreich's ataxia patients and in a mouse modelMyriam Rai, Elisabetta Soragni, C James Chou, et al.
Stem Cells and Development|November 16, 2006
A real-time PCR approach to evaluate adipogenic potential of amniotic fluid-derived human mesenchymal stem cellsPaola De Gemmis, Cristina Lapucci, Matteo Bertelli, et al.
Brain Communications|March 3, 2023
Proprioceptors-enriched neuronal cultures from induced pluripotent stem cells from Friedreich ataxia patients show altered transcriptomic and proteomic profiles, abnormal neurite extension, and impaired electrophysiological propertiesChiara Dionisi, Marine Chazalon, Myriam Rai, et al.
Human Molecular Genetics|February 9, 2017
Friedreich ataxia-induced pluripotent stem cell-derived neurons show a cellular phenotype that is corrected by a benzamide HDAC inhibitorFranca Codazzi, Amelié Hu, Myriam Rai, et al.
Plos One|October 18, 2007
Proprotein convertase subtilisin/kexin type 9 (PCSK9) gene is a risk factor of large-vessel atherosclerosis strokeShérine Abboud, Pekka J Karhunen, Dieter Lütjohann, et al.
Pageof 17