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Pediatrics
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April 2, 2016
Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study
Sarah Wong, Eleonora Napoli, Paula Krakowiak, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2012
Newborn screening and cascade testing for FMR1 mutations
Page 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 responses
Milo 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 syndrome
Ryu-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 Syndrome
Mittal 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 premutation
So-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 syndrome
Chantal 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 review
Adam 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 Syndrome
Poonnada 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 medicine
Gyu Song, Eleonora Napoli, Sarah Wong, et al.
Page
of 35
Search research articles
Search
Showing results (51-60 of 348) with videos related to
Sort By:
Page
of 35
Pediatrics
|
April 2, 2016
Role of p53, Mitochondrial DNA Deletions, and Paternal Age in Autism: A Case-Control Study
Sarah Wong, Eleonora Napoli, Paula Krakowiak, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2012
Newborn screening and cascade testing for FMR1 mutations
Page 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 responses
Milo 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 syndrome
Ryu-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 Syndrome
Mittal 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 premutation
So-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 syndrome
Chantal 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 review
Adam 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 Syndrome
Poonnada 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 medicine
Gyu Song, Eleonora Napoli, Sarah Wong, et al.
Page
of 35