Search research articles
Contact Us
Filters
Showing results (21-30 of 29) with videos related to
Page
of 3
Sort By:
You have reached the last page of results.
This site can display upto 29 results.
Pediatric Neurology
|
June 14, 2021
Clinical Profile and Long-Term Outcome in Neonatal Cerebral Sinus Venous Thrombosis
Isabella Herman, Cemal Karakas, Troy A Webber, et al.
Nature Genetics
|
October 28, 2003
Interaction of reelin signaling and Lis1 in brain development
Amir H Assadi, Guangcheng Zhang, Uwe Beffert, et al.
Epilepsy & Behavior : E&B
|
July 15, 2018
Open-label use of highly purified CBD (Epidiolex®) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes
Orrin Devinsky, Chloe Verducci, Elizabeth A Thiele, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2008
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2
William B Dobyns, Ghayda Mirzaa, Susan L Christian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2007
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region
Jonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.
American Journal of Human Genetics
|
April 9, 2024
The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing
Shenglan Li, Sen Zhao, Jefferson C Sinson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 20, 2023
TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system
Shyam K Akula, Jack H Marciano, Youngshin Lim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 4, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency
Ash Zawerton, Cyril Mignot, Ashley Sigafoos, et al.
Annals of Neurology
|
October 7, 2025
Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism
Hormos Salimi Dafsari, Celine Deneubourg, Kritarth Singh, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 29 results.
Pediatric Neurology
|
June 14, 2021
Clinical Profile and Long-Term Outcome in Neonatal Cerebral Sinus Venous Thrombosis
Isabella Herman, Cemal Karakas, Troy A Webber, et al.
Nature Genetics
|
October 28, 2003
Interaction of reelin signaling and Lis1 in brain development
Amir H Assadi, Guangcheng Zhang, Uwe Beffert, et al.
Epilepsy & Behavior : E&B
|
July 15, 2018
Open-label use of highly purified CBD (Epidiolex®) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes
Orrin Devinsky, Chloe Verducci, Elizabeth A Thiele, et al.
American Journal of Medical Genetics. Part A
|
June 7, 2008
Consistent chromosome abnormalities identify novel polymicrogyria loci in 1p36.3, 2p16.1-p23.1, 4q21.21-q22.1, 6q26-q27, and 21q2
William B Dobyns, Ghayda Mirzaa, Susan L Christian, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 2, 2007
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region
Jonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, et al.
American Journal of Human Genetics
|
April 9, 2024
The clinical utility and diagnostic implementation of human subject cell transdifferentiation followed by RNA sequencing
Shenglan Li, Sen Zhao, Jefferson C Sinson, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 20, 2023
TMEM161B regulates cerebral cortical gyration, Sonic Hedgehog signaling, and ciliary structure in the developing central nervous system
Shyam K Akula, Jack H Marciano, Youngshin Lim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 4, 2019
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency
Ash Zawerton, Cyril Mignot, Ashley Sigafoos, et al.
Annals of Neurology
|
October 7, 2025
Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism
Hormos Salimi Dafsari, Celine Deneubourg, Kritarth Singh, et al.
Page
of 3