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Flora Tassone

Showing results (51-60 of 348) with videos related to

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Pediatrics|April 2, 2016
Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control StudySarah Wong, Eleonora Napoli, Paula Krakowiak, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Newborn screening and cascade testing for FMR1 mutationsPage L Sorensen, Louise W Gane, Mark Yarborough, et al.
Plos One|April 11, 2014
Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responsesMilo Careaga, Destanie Rose, Flora Tassone, et al.
Brain : a Journal of Neurology|March 1, 2011
A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndromeRyu-ichiro Hashimoto, Alireza K Javan, Flora Tassone, et al.
Genes|October 27, 2022
Profiling Genome-Wide DNA Methylation in Children with Autism Spectrum Disorder and in Children with Fragile X SyndromeMittal Jasoliya, Jianlei Gu, Reem R AlOlaby, et al.
Journal of Psychiatric Research|September 19, 2013
Altered neural activity of magnitude estimation processing in adults with the fragile X premutationSo-Yeon Kim, Ryu-ichiro Hashimoto, Flora Tassone, et al.
Journal of Neurodevelopmental Disorders|August 28, 2014
The multiple molecular facets of fragile X-associated tremor/ataxia syndromeChantal Sellier, Karen Usdin, Chiara Pastori, et al.
American Journal of Medical Genetics. Part A|November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A reviewAdam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.
Frontiers in Genetics|June 1, 2022
<i>De Novo</i> Large Deletion Leading to Fragile X SyndromePoonnada Jiraanont, Esther Manor, Nazi Tabatadze, et al.
Molecular Medicine (Cambridge, Mass.)|July 8, 2016
Altered redox mitochondrial biology in the neurodegenerative disorder fragile X-tremor/ataxia syndrome: use of antioxidants in precision medicineGyu Song, Eleonora Napoli, Sarah Wong, et al.
Pageof 35

Showing results (51-60 of 348) with videos related to

Sort By:
Pageof 35
Pediatrics|April 2, 2016
Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control StudySarah Wong, Eleonora Napoli, Paula Krakowiak, et al.
American Journal of Medical Genetics. Part A|December 15, 2012
Newborn screening and cascade testing for FMR1 mutationsPage L Sorensen, Louise W Gane, Mark Yarborough, et al.
Plos One|April 11, 2014
Immune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responsesMilo Careaga, Destanie Rose, Flora Tassone, et al.
Brain : a Journal of Neurology|March 1, 2011
A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndromeRyu-ichiro Hashimoto, Alireza K Javan, Flora Tassone, et al.
Genes|October 27, 2022
Profiling Genome-Wide DNA Methylation in Children with Autism Spectrum Disorder and in Children with Fragile X SyndromeMittal Jasoliya, Jianlei Gu, Reem R AlOlaby, et al.
Journal of Psychiatric Research|September 19, 2013
Altered neural activity of magnitude estimation processing in adults with the fragile X premutationSo-Yeon Kim, Ryu-ichiro Hashimoto, Flora Tassone, et al.
Journal of Neurodevelopmental Disorders|August 28, 2014
The multiple molecular facets of fragile X-associated tremor/ataxia syndromeChantal Sellier, Karen Usdin, Chiara Pastori, et al.
American Journal of Medical Genetics. Part A|November 28, 2017
Rare FMR1 gene mutations causing fragile X syndrome: A reviewAdam F Sitzmann, Robert T Hagelstrom, Flora Tassone, et al.
Frontiers in Genetics|June 1, 2022
<i>De Novo</i> Large Deletion Leading to Fragile X SyndromePoonnada Jiraanont, Esther Manor, Nazi Tabatadze, et al.
Molecular Medicine (Cambridge, Mass.)|July 8, 2016
Altered redox mitochondrial biology in the neurodegenerative disorder fragile X-tremor/ataxia syndrome: use of antioxidants in precision medicineGyu Song, Eleonora Napoli, Sarah Wong, et al.
Pageof 35