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Kimberly Goodspeed

Showing results (11-20 of 32) with videos related to

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Journal of Child Neurology|January 11, 2018
Pitt-Hopkins Syndrome: A Review of Current Literature, Clinical Approach, and 23-Patient Case SeriesKimberly Goodspeed, Cassandra Newsom, Mary Ann Morris, et al.
Journal of Child Neurology|June 2, 2023
Electroencephalographic (EEG) Biomarkers in Genetic Neurodevelopmental DisordersKimberly Goodspeed, Dallas Armstrong, Alison Dolce, et al.
Annals of Clinical and Translational Neurology|December 20, 2018
Optical coherence tomography features in brothers with aspartylglucosaminuriaKimberly Goodspeed, Lana Harder, Samuel Hughes, et al.
Molecular Therapy. Advances|May 29, 2026
External controls for rare disease drug development: Lessons for emerging and advanced therapeutic modalitiesSamuel H Hughes, Lauren A Beretich, Matthew Fuller, et al.
JIMD Reports|September 14, 2022
A cross-sectional natural history study of aspartylglucosaminuriaKimberly Goodspeed, Daniel Horton, Andrea Lowden, et al.
Journal of Neurodevelopmental Disorders|June 27, 2022
Consistency of parent-report SLC6A1 data in Simons Searchlight with Provider-Based PublicationsJennifer M Bain, LeeAnne Green Snyder, Katherine L Helbig, et al.
NPJ Genomic Medicine|December 5, 2024
The genetic landscape of autism spectrum disorder in an ancestrally diverse cohortAshlesha Gogate, Kiran Kaur, Raida Khalil, et al.
Frontiers in Neurology|July 18, 2022
Gene Therapy: Novel Approaches to Targeting Monogenic EpilepsiesKimberly Goodspeed, Rachel M Bailey, Suyash Prasad, et al.
Cell Genomics|July 26, 2023
The genetics of autism spectrum disorder in an East African familial cohortIslam Oguz Tuncay, Darlene DeVries, Ashlesha Gogate, et al.
Frontiers in Neuroscience|March 10, 2023
Patterns of developmental regression and associated clinical characteristics in SLC6A1-related disorderSanjana Kalvakuntla, MinJae Lee, Wendy K Chung, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of Child Neurology|January 11, 2018
Pitt-Hopkins Syndrome: A Review of Current Literature, Clinical Approach, and 23-Patient Case SeriesKimberly Goodspeed, Cassandra Newsom, Mary Ann Morris, et al.
Journal of Child Neurology|June 2, 2023
Electroencephalographic (EEG) Biomarkers in Genetic Neurodevelopmental DisordersKimberly Goodspeed, Dallas Armstrong, Alison Dolce, et al.
Annals of Clinical and Translational Neurology|December 20, 2018
Optical coherence tomography features in brothers with aspartylglucosaminuriaKimberly Goodspeed, Lana Harder, Samuel Hughes, et al.
Molecular Therapy. Advances|May 29, 2026
External controls for rare disease drug development: Lessons for emerging and advanced therapeutic modalitiesSamuel H Hughes, Lauren A Beretich, Matthew Fuller, et al.
JIMD Reports|September 14, 2022
A cross-sectional natural history study of aspartylglucosaminuriaKimberly Goodspeed, Daniel Horton, Andrea Lowden, et al.
Journal of Neurodevelopmental Disorders|June 27, 2022
Consistency of parent-report SLC6A1 data in Simons Searchlight with Provider-Based PublicationsJennifer M Bain, LeeAnne Green Snyder, Katherine L Helbig, et al.
NPJ Genomic Medicine|December 5, 2024
The genetic landscape of autism spectrum disorder in an ancestrally diverse cohortAshlesha Gogate, Kiran Kaur, Raida Khalil, et al.
Frontiers in Neurology|July 18, 2022
Gene Therapy: Novel Approaches to Targeting Monogenic EpilepsiesKimberly Goodspeed, Rachel M Bailey, Suyash Prasad, et al.
Cell Genomics|July 26, 2023
The genetics of autism spectrum disorder in an East African familial cohortIslam Oguz Tuncay, Darlene DeVries, Ashlesha Gogate, et al.
Frontiers in Neuroscience|March 10, 2023
Patterns of developmental regression and associated clinical characteristics in SLC6A1-related disorderSanjana Kalvakuntla, MinJae Lee, Wendy K Chung, et al.
Pageof 4