Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Christine Spaeth

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Epileptic Disorders : International Epilepsy Journal with Videotape|March 27, 2021
Epilepsy phenotypes associated with MAP1B-related brain malformationsRavindra Arya, Christine Spaeth, Wenying Zhang
Pediatric Neurology|May 31, 2016
Correlation Among Genotype, Phenotype, and Histology in Neuronal Ceroid Lipofuscinoses: An Individual Patient Data Meta-AnalysisGewalin Aungaroon, Barbara Hallinan, Puneet Jain, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 17, 2017
GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotypeRavindra Arya, Christine Spaeth, Donald L Gilbert, et al.
Journal of Child Neurology|December 26, 2022
Imaging Similarities Between Oral-Facial-Digital Syndrome Type 1 and Aicardi Syndrome: Prenatal and Postnatal Magnetic Resonance Imaging (MRI) Findings in 4 PatientsCharu Venkatesan, Elizabeth Countee, Beatrix Wong, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Epileptic Disorders : International Epilepsy Journal with Videotape|March 27, 2021
Epilepsy phenotypes associated with MAP1B-related brain malformationsRavindra Arya, Christine Spaeth, Wenying Zhang
Pediatric Neurology|May 31, 2016
Correlation Among Genotype, Phenotype, and Histology in Neuronal Ceroid Lipofuscinoses: An Individual Patient Data Meta-AnalysisGewalin Aungaroon, Barbara Hallinan, Puneet Jain, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|February 17, 2017
GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotypeRavindra Arya, Christine Spaeth, Donald L Gilbert, et al.
Journal of Child Neurology|December 26, 2022
Imaging Similarities Between Oral-Facial-Digital Syndrome Type 1 and Aicardi Syndrome: Prenatal and Postnatal Magnetic Resonance Imaging (MRI) Findings in 4 PatientsCharu Venkatesan, Elizabeth Countee, Beatrix Wong, et al.
Annals of Clinical and Translational Neurology|July 1, 2015
De novo mutations in KIF1A cause progressive encephalopathy and brain atrophySahar Esmaeeli Nieh, Maura R Z Madou, Minhajuddin Sirajuddin, et al.
Pageof 1