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Movement Disorders Clinical Practice
|
November 9, 2020
Women with Fragile X-associated Tremor/Ataxia Syndrome
Andrea Schneider, Scott Summers, Flora Tassone, et al.
Annals of Neurology
|
May 6, 2003
Tremor and ataxia in fragile X premutation carriers: blinded videotape study
Elizabeth Berry-Kravis, Foster Lewin, Joanne Wuu, et al.
Genes
|
March 28, 2024
Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome
YeEun Tak, Andrea Schneider, Ellery Santos, et al.
Molecular Genetics & Genomic Medicine
|
January 4, 2020
Developmental aspects of FXAND in a man with the FMR1 premutation
Ellery Santos, Chinelo Emeka-Nwonovo, Jun Yi Wang, et al.
Mitochondrion
|
July 19, 2014
High-throughput screening of FDA-approved drugs using oxygen biosensor plates reveals secondary mitofunctional effects
Sunil Sahdeo, Alexey Tomilov, Kelly Komachi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 25, 2017
Iron accumulation and dysregulation in the putamen in fragile X-associated tremor/ataxia syndrome
Jeanelle Ariza, Hailee Rogers, Anna Hartvigsen, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
May 25, 2006
Dementia with mood symptoms in a fragile X premutation carrier with the fragile X-associated tremor/ataxia syndrome: clinical intervention with donepezil and venlafaxine
James A Bourgeois, Faraz Farzin, James A Brunberg, et al.
The Journal of Molecular Diagnostics : JMD
|
November 1, 2005
An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene
Alessandro Saluto, Alessandro Brussino, Flora Tassone, et al.
Translational Psychiatry
|
June 25, 2020
Elevated FMR1-mRNA and lowered FMRP - A double-hit mechanism for psychiatric features in men with FMR1 premutations
Andrea Schneider, Tri Indah Winarni, Ana María Cabal-Herrera, et al.
Case Reports in Genetics
|
January 22, 2025
Novel p.Arg534del Mutation and MTHFR C667T Polymorphism in Fragile X Syndrome (FXS) With Autism Spectrum Phenotype: A Case Report
Hasan Hasan, Ellery R Santos, Seyedeh Ala Mokhtabad Amrei, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Movement Disorders Clinical Practice
|
November 9, 2020
Women with Fragile X-associated Tremor/Ataxia Syndrome
Andrea Schneider, Scott Summers, Flora Tassone, et al.
Annals of Neurology
|
May 6, 2003
Tremor and ataxia in fragile X premutation carriers: blinded videotape study
Elizabeth Berry-Kravis, Foster Lewin, Joanne Wuu, et al.
Genes
|
March 28, 2024
Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome
YeEun Tak, Andrea Schneider, Ellery Santos, et al.
Molecular Genetics & Genomic Medicine
|
January 4, 2020
Developmental aspects of FXAND in a man with the FMR1 premutation
Ellery Santos, Chinelo Emeka-Nwonovo, Jun Yi Wang, et al.
Mitochondrion
|
July 19, 2014
High-throughput screening of FDA-approved drugs using oxygen biosensor plates reveals secondary mitofunctional effects
Sunil Sahdeo, Alexey Tomilov, Kelly Komachi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 25, 2017
Iron accumulation and dysregulation in the putamen in fragile X-associated tremor/ataxia syndrome
Jeanelle Ariza, Hailee Rogers, Anna Hartvigsen, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences
|
May 25, 2006
Dementia with mood symptoms in a fragile X premutation carrier with the fragile X-associated tremor/ataxia syndrome: clinical intervention with donepezil and venlafaxine
James A Bourgeois, Faraz Farzin, James A Brunberg, et al.
The Journal of Molecular Diagnostics : JMD
|
November 1, 2005
An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene
Alessandro Saluto, Alessandro Brussino, Flora Tassone, et al.
Translational Psychiatry
|
June 25, 2020
Elevated FMR1-mRNA and lowered FMRP - A double-hit mechanism for psychiatric features in men with FMR1 premutations
Andrea Schneider, Tri Indah Winarni, Ana María Cabal-Herrera, et al.
Case Reports in Genetics
|
January 22, 2025
Novel p.Arg534del Mutation and MTHFR C667T Polymorphism in Fragile X Syndrome (FXS) With Autism Spectrum Phenotype: A Case Report
Hasan Hasan, Ellery R Santos, Seyedeh Ala Mokhtabad Amrei, et al.
Page
of 4