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Brain Sciences
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November 24, 2022
Relationships of Motor Changes with Cognitive and Neuropsychiatric Features in FMR1 Male Carriers Affected with Fragile X-Associated Tremor/Ataxia Syndrome
Darren R Hocking, Danuta Z Loesch, Paige Stimpson, et al.
BMC Medical Genetics
|
October 15, 2014
Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR
Vicki J Hwang, Dianna Maar, John Regan, et al.
European Journal of Medical Genetics
|
December 2, 2017
A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome
Matthew Jensen, R Frank Kooy, Tony J Simon, et al.
Frontiers in Genetics
|
September 14, 2018
Impact of
Eleonora Napoli, Andrea Schneider, Randi Hagerman, et al.
Movement Disorders Clinical Practice
|
November 9, 2020
Women with Fragile X-associated Tremor/Ataxia Syndrome
Andrea Schneider, Scott Summers, Flora Tassone, et al.
Cerebellum & Ataxias
|
June 12, 2021
Relationships between motor scores and cognitive functioning in FMR1 female premutation X carriers indicate early involvement of cerebello-cerebral pathways
Elsdon Storey, Minh Q Bui, Paige Stimpson, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2011
Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation
Kirin Basuta, Vivien Narcisa, Alyssa Chavez, et al.
Frontiers in Molecular Neuroscience
|
May 4, 2026
Integrated multi-omics profiling reveals novel molecular biomarkers and pathways associated with Fragile X-associated tremor/ataxia syndrome
Marwa Zafarullah, Matthew Ponzini, Kyoungmi Kim, et al.
Frontiers in Neurology
|
June 21, 2024
Cognitive status correlates of subclinical action tremor in female carriers of FMR1 premutation
Danuta Z Loesch, Anna Atkinson, Deborah A Hall, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 4, 2011
MAOA, DBH, and SLC6A4 variants in CHARGE: a case-control study of autism spectrum disorders
Flora Tassone, Lihong Qi, Wenting Zhang, et al.
Page
of 35
Search research articles
Search
Showing results (71-80 of 348) with videos related to
Sort By:
Page
of 35
Brain Sciences
|
November 24, 2022
Relationships of Motor Changes with Cognitive and Neuropsychiatric Features in FMR1 Male Carriers Affected with Fragile X-Associated Tremor/Ataxia Syndrome
Darren R Hocking, Danuta Z Loesch, Paige Stimpson, et al.
BMC Medical Genetics
|
October 15, 2014
Mapping the deletion endpoints in individuals with 22q11.2 deletion syndrome by droplet digital PCR
Vicki J Hwang, Dianna Maar, John Regan, et al.
European Journal of Medical Genetics
|
December 2, 2017
A higher rare CNV burden in the genetic background potentially contributes to intellectual disability phenotypes in 22q11.2 deletion syndrome
Matthew Jensen, R Frank Kooy, Tony J Simon, et al.
Frontiers in Genetics
|
September 14, 2018
Impact of
Eleonora Napoli, Andrea Schneider, Randi Hagerman, et al.
Movement Disorders Clinical Practice
|
November 9, 2020
Women with Fragile X-associated Tremor/Ataxia Syndrome
Andrea Schneider, Scott Summers, Flora Tassone, et al.
Cerebellum & Ataxias
|
June 12, 2021
Relationships between motor scores and cognitive functioning in FMR1 female premutation X carriers indicate early involvement of cerebello-cerebral pathways
Elsdon Storey, Minh Q Bui, Paige Stimpson, et al.
American Journal of Medical Genetics. Part A
|
February 24, 2011
Clinical phenotypes of a juvenile sibling pair carrying the fragile X premutation
Kirin Basuta, Vivien Narcisa, Alyssa Chavez, et al.
Frontiers in Molecular Neuroscience
|
May 4, 2026
Integrated multi-omics profiling reveals novel molecular biomarkers and pathways associated with Fragile X-associated tremor/ataxia syndrome
Marwa Zafarullah, Matthew Ponzini, Kyoungmi Kim, et al.
Frontiers in Neurology
|
June 21, 2024
Cognitive status correlates of subclinical action tremor in female carriers of FMR1 premutation
Danuta Z Loesch, Anna Atkinson, Deborah A Hall, et al.
Autism Research : Official Journal of the International Society for Autism Research
|
May 4, 2011
MAOA, DBH, and SLC6A4 variants in CHARGE: a case-control study of autism spectrum disorders
Flora Tassone, Lihong Qi, Wenting Zhang, et al.
Page
of 35