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

Adeline Vanderver

Showing results (91-100 of 217) with videos related to

Pageof 22
Sort By:
Pediatric Neurology|October 8, 2021
Reliability of the Telemedicine Application of the Gross Motor Function Measure-88 in Patients With LeukodystrophyFrancesco Gavazzi, Laura Adang, Amy Waldman, et al.
Annals of Neurology|December 9, 2015
Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathyGuy Helman, Ljubica Caldovic, Matthew T Whitehead, et al.
Molecular Genetics and Metabolism|March 20, 2025
Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disordersAnthony C T Cheung, Erminia Di Pietro, Catherine Argyriou, et al.
NPJ Genomic Medicine|January 11, 2024
Kagami Ogata syndrome: a small deletion refines critical region for imprintingGonench Kilich, Kelly Hassey, Edward M Behrens, et al.
Journal of Child Neurology|December 24, 2014
Early-Onset Aicardi-Goutières Syndrome: Magnetic Resonance Imaging (MRI) Pattern RecognitionAdeline Vanderver, Morgan Prust, Nadja Kadom, et al.
Molecular Genetics and Metabolism|July 4, 2012
Neurotransmitter abnormalities and response to supplementation in SPG11Adeline Vanderver, Davide Tonduti, Sarah Auerbach, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 11, 2014
Comprehensive immunophenotyping of cerebrospinal fluid cells in patients with neuroimmunological diseasesSungpil Han, Yen Chih Lin, Tianxia Wu, et al.
Archives of Neurology|February 8, 2012
Novel infantile-onset leukoencephalopathy with high lactate level and slow improvementMarjan E Steenweg, Adeline Vanderver, Berten Ceulemans, et al.
Brain : a Journal of Neurology|October 4, 2017
Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophyImen Dorboz, Chiara Aiello, Cas Simons, et al.
Annals of Neurology|June 12, 2014
Hypomyelinating leukodystrophies: translational research progress and prospectsPetra J W Pouwels, Adeline Vanderver, Genevieve Bernard, et al.
Pageof 22

Showing results (91-100 of 217) with videos related to

Sort By:
Pageof 22
Pediatric Neurology|October 8, 2021
Reliability of the Telemedicine Application of the Gross Motor Function Measure-88 in Patients With LeukodystrophyFrancesco Gavazzi, Laura Adang, Amy Waldman, et al.
Annals of Neurology|December 9, 2015
Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathyGuy Helman, Ljubica Caldovic, Matthew T Whitehead, et al.
Molecular Genetics and Metabolism|March 20, 2025
Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disordersAnthony C T Cheung, Erminia Di Pietro, Catherine Argyriou, et al.
NPJ Genomic Medicine|January 11, 2024
Kagami Ogata syndrome: a small deletion refines critical region for imprintingGonench Kilich, Kelly Hassey, Edward M Behrens, et al.
Journal of Child Neurology|December 24, 2014
Early-Onset Aicardi-Goutières Syndrome: Magnetic Resonance Imaging (MRI) Pattern RecognitionAdeline Vanderver, Morgan Prust, Nadja Kadom, et al.
Molecular Genetics and Metabolism|July 4, 2012
Neurotransmitter abnormalities and response to supplementation in SPG11Adeline Vanderver, Davide Tonduti, Sarah Auerbach, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 11, 2014
Comprehensive immunophenotyping of cerebrospinal fluid cells in patients with neuroimmunological diseasesSungpil Han, Yen Chih Lin, Tianxia Wu, et al.
Archives of Neurology|February 8, 2012
Novel infantile-onset leukoencephalopathy with high lactate level and slow improvementMarjan E Steenweg, Adeline Vanderver, Berten Ceulemans, et al.
Brain : a Journal of Neurology|October 4, 2017
Biallelic mutations in the homeodomain of NKX6-2 underlie a severe hypomyelinating leukodystrophyImen Dorboz, Chiara Aiello, Cas Simons, et al.
Annals of Neurology|June 12, 2014
Hypomyelinating leukodystrophies: translational research progress and prospectsPetra J W Pouwels, Adeline Vanderver, Genevieve Bernard, et al.
Pageof 22