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Kimberly Goodspeed

Showing results (21-30 of 32) with videos related to

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Genes|September 23, 2022
SLC13A5 Deficiency Disorder: From Genetics to Gene TherapyKimberly Goodspeed, Judy S Liu, Kimberly L Nye, et al.
Epilepsy Research|December 24, 2025
SLC13A5 citrate transporter disorder epilepsy phenotypeCan Ozlu, Emily M Spelbrink, Tanya L Brown, et al.
Frontiers in Neuroscience|February 6, 2023
A draft conceptual model of SLC6A1 neurodevelopmental disorderKimberly Goodspeed, Lindsay R Mosca, Nicole C Weitzel, et al.
NPJ Genomic Medicine|February 22, 2022
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variantsIslam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, et al.
Genes|October 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter DisorderRaegan M Adams, Can Ozlu, Lauren E Bailey, et al.
Developmental Medicine and Child Neurology|December 22, 2024
Developmental phenotype and quality of life in SLC13A5 citrate transporter disorderCan Ozlu, Raegan M Adams, Rayann M Solidum, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2020
Current Clinical Applications of In Vivo Gene Therapy with AAVsJerry R Mendell, Samiah A Al-Zaidy, Louise R Rodino-Klapac, et al.
Frontiers in Neuroscience|July 28, 2023
Intrafamilial variability in <i>SLC6A1</i>-related neurodevelopmental disordersBenedetta Kassabian, Christina Dühring Fenger, Marjolaine Willems, et al.
Frontiers in Neuroscience|August 28, 2023
Corrigendum: Intrafamilial variability in <i>SLC6A1</i>-related neurodevelopmental disordersBenedetta Kassabian, Christina Dühring Fenger, Marjolaine Willems, et al.
Brain Communications|November 26, 2020
Current knowledge of SLC6A1-related neurodevelopmental disordersKimberly Goodspeed, Eduardo Pérez-Palma, Sumaiya Iqbal, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Genes|September 23, 2022
SLC13A5 Deficiency Disorder: From Genetics to Gene TherapyKimberly Goodspeed, Judy S Liu, Kimberly L Nye, et al.
Epilepsy Research|December 24, 2025
SLC13A5 citrate transporter disorder epilepsy phenotypeCan Ozlu, Emily M Spelbrink, Tanya L Brown, et al.
Frontiers in Neuroscience|February 6, 2023
A draft conceptual model of SLC6A1 neurodevelopmental disorderKimberly Goodspeed, Lindsay R Mosca, Nicole C Weitzel, et al.
NPJ Genomic Medicine|February 22, 2022
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variantsIslam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, et al.
Genes|October 26, 2024
Sleep Abnormalities in SLC13A5 Citrate Transporter DisorderRaegan M Adams, Can Ozlu, Lauren E Bailey, et al.
Developmental Medicine and Child Neurology|December 22, 2024
Developmental phenotype and quality of life in SLC13A5 citrate transporter disorderCan Ozlu, Raegan M Adams, Rayann M Solidum, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2020
Current Clinical Applications of In Vivo Gene Therapy with AAVsJerry R Mendell, Samiah A Al-Zaidy, Louise R Rodino-Klapac, et al.
Frontiers in Neuroscience|July 28, 2023
Intrafamilial variability in <i>SLC6A1</i>-related neurodevelopmental disordersBenedetta Kassabian, Christina Dühring Fenger, Marjolaine Willems, et al.
Frontiers in Neuroscience|August 28, 2023
Corrigendum: Intrafamilial variability in <i>SLC6A1</i>-related neurodevelopmental disordersBenedetta Kassabian, Christina Dühring Fenger, Marjolaine Willems, et al.
Brain Communications|November 26, 2020
Current knowledge of SLC6A1-related neurodevelopmental disordersKimberly Goodspeed, Eduardo Pérez-Palma, Sumaiya Iqbal, et al.
Pageof 4