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International Journal of Molecular Sciences
|
August 10, 2024
Apolipoproteine and <i>KLOTHO</i> Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome
Tri Indah Winarni, Ye Hyun Hwang, Susan M Rivera, et al.
Molecular Neurobiology
|
September 7, 2018
Allopregnanolone Treatment Improves Plasma Metabolomic Profile Associated with GABA Metabolism in Fragile X-Associated Tremor/Ataxia Syndrome: a Pilot Study
Eleonora Napoli, Andrea Schneider, Jun Yi Wang, et al.
Scientific Reports
|
September 30, 2020
Cortical gyrification and its relationships with molecular measures and cognition in children with the FMR1 premutation
Jun Yi Wang, Merna Danial, Cyrus Soleymanzadeh, et al.
Frontiers in Neuroscience
|
May 6, 2016
Premutation in the Fragile X Mental Retardation 1 (FMR1) Gene Affects Maternal Zn-milk and Perinatal Brain Bioenergetics and Scaffolding
Eleonora Napoli, Catherine Ross-Inta, Gyu Song, et al.
Frontiers in Neurology
|
February 25, 2022
Clinical and Molecular Correlates of Abnormal Changes in the Cerebellum and Globus Pallidus in Fragile X Premutation
Jun Yi Wang, Jim Grigsby, Diego Placido, et al.
Human Molecular Genetics
|
April 3, 2012
Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone
Zhengyu Cao, Susan Hulsizer, Flora Tassone, et al.
American Journal of Medical Genetics. Part A
|
April 25, 2012
Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS)
Alyssa A Hamlin, Dina Sukharev, Luis Campos, et al.
JAMA
|
December 2, 2010
Mitochondrial dysfunction in autism
Cecilia Giulivi, Yi-Fan Zhang, Alicja Omanska-Klusek, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder
Catalina García-Nonell, Eugenia Rigau Ratera, Susan Harris, et al.
Human Molecular Genetics
|
January 28, 2014
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size
Anna Lisa Ludwig, Glenda M Espinal, Dalyir I Pretto, et al.
Page
of 35
Search research articles
Search
Showing results (191-200 of 348) with videos related to
Sort By:
Page
of 35
International Journal of Molecular Sciences
|
August 10, 2024
Apolipoproteine and <i>KLOTHO</i> Gene Variants Do Not Affect the Penetrance of Fragile X-Associated Tremor/Ataxia Syndrome
Tri Indah Winarni, Ye Hyun Hwang, Susan M Rivera, et al.
Molecular Neurobiology
|
September 7, 2018
Allopregnanolone Treatment Improves Plasma Metabolomic Profile Associated with GABA Metabolism in Fragile X-Associated Tremor/Ataxia Syndrome: a Pilot Study
Eleonora Napoli, Andrea Schneider, Jun Yi Wang, et al.
Scientific Reports
|
September 30, 2020
Cortical gyrification and its relationships with molecular measures and cognition in children with the FMR1 premutation
Jun Yi Wang, Merna Danial, Cyrus Soleymanzadeh, et al.
Frontiers in Neuroscience
|
May 6, 2016
Premutation in the Fragile X Mental Retardation 1 (FMR1) Gene Affects Maternal Zn-milk and Perinatal Brain Bioenergetics and Scaffolding
Eleonora Napoli, Catherine Ross-Inta, Gyu Song, et al.
Frontiers in Neurology
|
February 25, 2022
Clinical and Molecular Correlates of Abnormal Changes in the Cerebellum and Globus Pallidus in Fragile X Premutation
Jun Yi Wang, Jim Grigsby, Diego Placido, et al.
Human Molecular Genetics
|
April 3, 2012
Clustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone
Zhengyu Cao, Susan Hulsizer, Flora Tassone, et al.
American Journal of Medical Genetics. Part A
|
April 25, 2012
Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS)
Alyssa A Hamlin, Dina Sukharev, Luis Campos, et al.
JAMA
|
December 2, 2010
Mitochondrial dysfunction in autism
Cecilia Giulivi, Yi-Fan Zhang, Alicja Omanska-Klusek, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder
Catalina García-Nonell, Eugenia Rigau Ratera, Susan Harris, et al.
Human Molecular Genetics
|
January 28, 2014
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size
Anna Lisa Ludwig, Glenda M Espinal, Dalyir I Pretto, et al.
Page
of 35