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Paul Hagerman

Showing results (11-20 of 31) with videos related to

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Movement Disorders Clinical Practice|November 9, 2020
Women with Fragile X-associated Tremor/Ataxia SyndromeAndrea Schneider, Scott Summers, Flora Tassone, et al.
Annals of Neurology|May 6, 2003
Tremor and ataxia in fragile X premutation carriers: blinded videotape studyElizabeth Berry-Kravis, Foster Lewin, Joanne Wuu, et al.
Genes|March 28, 2024
Unmethylated Mosaic Full Mutation Males without Fragile X SyndromeYeEun Tak, Andrea Schneider, Ellery Santos, et al.
Molecular Genetics & Genomic Medicine|January 4, 2020
Developmental aspects of FXAND in a man with the FMR1 premutationEllery 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 effectsSunil 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 syndromeJeanelle 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 venlafaxineJames 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 geneAlessandro 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 premutationsAndrea 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 ReportHasan Hasan, Ellery R Santos, Seyedeh Ala Mokhtabad Amrei, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Movement Disorders Clinical Practice|November 9, 2020
Women with Fragile X-associated Tremor/Ataxia SyndromeAndrea Schneider, Scott Summers, Flora Tassone, et al.
Annals of Neurology|May 6, 2003
Tremor and ataxia in fragile X premutation carriers: blinded videotape studyElizabeth Berry-Kravis, Foster Lewin, Joanne Wuu, et al.
Genes|March 28, 2024
Unmethylated Mosaic Full Mutation Males without Fragile X SyndromeYeEun Tak, Andrea Schneider, Ellery Santos, et al.
Molecular Genetics & Genomic Medicine|January 4, 2020
Developmental aspects of FXAND in a man with the FMR1 premutationEllery 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 effectsSunil 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 syndromeJeanelle 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 venlafaxineJames 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 geneAlessandro 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 premutationsAndrea 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 ReportHasan Hasan, Ellery R Santos, Seyedeh Ala Mokhtabad Amrei, et al.
Pageof 4