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

Brain & development

Showing results (1471-1480 of 4,777) with videos related to

Pageof 478
Sort By:
Brain & Development|July 26, 2018
Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndromeYusuke Takezawa, Hiromi Fujie, Atsuo Kikuchi, et al.
Brain & Development|June 5, 2018
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutationsPauline Marzin, Cyril Mignot, Nathalie Dorison, et al.
Brain & Development|May 27, 2018
Neurodevelopmental outcomes in children with prenatally diagnosed corpus callosal abnormalitiesHye-Ryun Yeh, Hyo-Kyoung Park, Hyun-Jin Kim, et al.
Brain & Development|May 5, 2018
Spontaneous movements of preterm infants is associated with outcome of gross motor developmentSaori Miyagishima, Tadayoshi Asaka, Kaori Kamatsuka, et al.
Brain & Development|December 22, 1999
Sleep abnormalities in mentally retarded autistic subjects: Down's syndrome with mental retardation and normal subjectsM Diomedi, P Curatolo, A Scalise, et al.
Brain & Development|December 22, 1999
Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boyK Suwa, T Yamagata, M Y Momoi, et al.
Brain & Development|March 21, 2000
Head stability during whole body movements in spastic diplegiaB Dan, E Bouillot, A Bengoetxea, et al.
Brain & Development|March 21, 2000
Plasmapheresis in a child affected by acute disseminated encephalomyelitisP Balestri, S Grosso, A Acquaviva, et al.
Brain & Development|March 21, 2000
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic diseaseM A Al-Essa, S M Bakheet, Z J Patay, et al.
Brain & Development|March 21, 2000
Congenital myotonic dystrophy: report of paternal transmissionY Tanaka, Y Suzuki, N Shimozawa, et al.
Pageof 478

Showing results (1471-1480 of 4,777) with videos related to

Sort By:
Pageof 478
Brain & Development|July 26, 2018
Novel IARS2 mutations in Japanese siblings with CAGSSS, Leigh, and West syndromeYusuke Takezawa, Hiromi Fujie, Atsuo Kikuchi, et al.
Brain & Development|June 5, 2018
Early-onset encephalopathy with paroxysmal movement disorders and epileptic seizures without hemiplegic attacks: About three children with novel ATP1A3 mutationsPauline Marzin, Cyril Mignot, Nathalie Dorison, et al.
Brain & Development|May 27, 2018
Neurodevelopmental outcomes in children with prenatally diagnosed corpus callosal abnormalitiesHye-Ryun Yeh, Hyo-Kyoung Park, Hyun-Jin Kim, et al.
Brain & Development|May 5, 2018
Spontaneous movements of preterm infants is associated with outcome of gross motor developmentSaori Miyagishima, Tadayoshi Asaka, Kaori Kamatsuka, et al.
Brain & Development|December 22, 1999
Sleep abnormalities in mentally retarded autistic subjects: Down's syndrome with mental retardation and normal subjectsM Diomedi, P Curatolo, A Scalise, et al.
Brain & Development|December 22, 1999
Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boyK Suwa, T Yamagata, M Y Momoi, et al.
Brain & Development|March 21, 2000
Head stability during whole body movements in spastic diplegiaB Dan, E Bouillot, A Bengoetxea, et al.
Brain & Development|March 21, 2000
Plasmapheresis in a child affected by acute disseminated encephalomyelitisP Balestri, S Grosso, A Acquaviva, et al.
Brain & Development|March 21, 2000
Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography (FDG PET), MRI of the brain and biochemical observations in a patient with 4-hydroxybutyric aciduria; a progressive neurometabolic diseaseM A Al-Essa, S M Bakheet, Z J Patay, et al.
Brain & Development|March 21, 2000
Congenital myotonic dystrophy: report of paternal transmissionY Tanaka, Y Suzuki, N Shimozawa, et al.
Pageof 478