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Journal of Neurodevelopmental Disorders
|
March 24, 2022
Neuropsychological changes in FMR1 premutation carriers and onset of fragile X-associated tremor/ataxia syndrome
Jessica Famula, Emilio Ferrer, Randi J Hagerman, et al.
Intractable & Rare Diseases Research
|
January 22, 2015
Parent-delivered touchscreen intervention for children with fragile X syndrome
María Díez-Juan, Andrea Schneider, Tiffany Phillips, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2014
Association between macroorchidism and intelligence in FMR1 premutation carriers
Reymundo Lozano, Scott Summers, Cristina Lozano, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
February 28, 2024
Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome
Marwa Zafarullah, Kathleen Angkustsiri, Austin Quach, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
March 14, 2007
Early acceleration of head circumference in children with fragile x syndrome and autism
Sufen Chiu, Jacob A Wegelin, Jeremy Blank, et al.
Frontiers in Genetics
|
April 30, 2020
Molecular Biomarkers Predictive of Sertraline Treatment Response in Young Children With Autism Spectrum Disorder
Reem Rafik Alolaby, Poonnada Jiraanont, Blythe Durbin-Johnson, et al.
Annals of Neurology
|
June 3, 2025
Longitudinal Analysis of Neuroradiological Biomarkers for Fragile X-Associated Tremor/Ataxia Syndrome and Implications for Clinical Trials
David Hessl, Jun Yi Wang, Glenda Espinal, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2012
A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male
Page L Sorensen, Kirin Basuta, Guadalupe Mendoza-Morales, et al.
Archives of Neurology
|
April 17, 2008
Abnormal nerve conduction features in fragile X premutation carriers
Kultida Soontarapornchai, Ricardo Maselli, Grace Fenton-Farrell, et al.
Journal of Autism and Developmental Disorders
|
July 7, 2012
Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study
Flora Tassone, Nimrah S Choudhary, Federica Tassone, et al.
Page
of 35
Search research articles
Search
Showing results (111-120 of 348) with videos related to
Sort By:
Page
of 35
Journal of Neurodevelopmental Disorders
|
March 24, 2022
Neuropsychological changes in FMR1 premutation carriers and onset of fragile X-associated tremor/ataxia syndrome
Jessica Famula, Emilio Ferrer, Randi J Hagerman, et al.
Intractable & Rare Diseases Research
|
January 22, 2015
Parent-delivered touchscreen intervention for children with fragile X syndrome
María Díez-Juan, Andrea Schneider, Tiffany Phillips, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2014
Association between macroorchidism and intelligence in FMR1 premutation carriers
Reymundo Lozano, Scott Summers, Cristina Lozano, et al.
Metabolomics : Official Journal of the Metabolomic Society
|
February 28, 2024
Untargeted metabolomic, and proteomic analysis identifies metabolic biomarkers and pathway alterations in individuals with 22q11.2 deletion syndrome
Marwa Zafarullah, Kathleen Angkustsiri, Austin Quach, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP
|
March 14, 2007
Early acceleration of head circumference in children with fragile x syndrome and autism
Sufen Chiu, Jacob A Wegelin, Jeremy Blank, et al.
Frontiers in Genetics
|
April 30, 2020
Molecular Biomarkers Predictive of Sertraline Treatment Response in Young Children With Autism Spectrum Disorder
Reem Rafik Alolaby, Poonnada Jiraanont, Blythe Durbin-Johnson, et al.
Annals of Neurology
|
June 3, 2025
Longitudinal Analysis of Neuroradiological Biomarkers for Fragile X-Associated Tremor/Ataxia Syndrome and Implications for Clinical Trials
David Hessl, Jun Yi Wang, Glenda Espinal, et al.
American Journal of Medical Genetics. Part A
|
April 11, 2012
A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male
Page L Sorensen, Kirin Basuta, Guadalupe Mendoza-Morales, et al.
Archives of Neurology
|
April 17, 2008
Abnormal nerve conduction features in fragile X premutation carriers
Kultida Soontarapornchai, Ricardo Maselli, Grace Fenton-Farrell, et al.
Journal of Autism and Developmental Disorders
|
July 7, 2012
Identification of expanded alleles of the FMR1 Gene in the CHildhood Autism Risks from Genes and Environment (CHARGE) study
Flora Tassone, Nimrah S Choudhary, Federica Tassone, et al.
Page
of 35