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

Evangeline Wassmer

Showing results (1-10 of 120) with videos related to

Pageof 12
Sort By:
Developmental Medicine and Child Neurology|July 20, 2010
Mechanical ventilation in children with severe neurological impairmentShyam Mariguddi, Evangeline Wassmer
Journal of Child Neurology|December 17, 2008
Simultaneous peripheral and central demyelinationEvangeline Wassmer, William P Whitehouse
Journal of Child Neurology|January 15, 2008
Diagnostic yield of brain biopsies in children presenting to neurologySunita Venkateswaran, Cynthia Hawkins, Evangeline Wassmer
Biochimica Et Biophysica Acta. Biomembranes|September 12, 2021
Pathogenic antibodies to AQP4: Neuromyelitis optica spectrum disorder (NMOSD)Sukhvir K Wright, Evangeline Wassmer, Angela Vincent
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 4, 2025
Observational evidence of the treatment efficacy of IVIG as maintenance therapy for pediatric MOGADDaniel Griffiths-King, Evangeline Wassmer, Sukhvir K Wright
Archives of Disease in Childhood|January 25, 2020
Wilson disease in children and adolescentsMeranthi Fernando, Indra van Mourik, Evangeline Wassmer, et al.
Pediatric Neurology|July 25, 2003
Clinical spectrum associated with cerebellar hypoplasiaEvangeline Wassmer, Paul Davies, William P Whitehouse, et al.
Developmental Medicine and Child Neurology|February 12, 2011
Hereditary motor sensory neuropathy (type 1) presenting with transient and persistent central nervous system manifestations: a novel genetic mutationMichael Absoud, Louise Brueton, Rajat Gupta, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 20, 2014
RANBP2 mutation and acute necrotizing encephalopathy: 2 cases and a literature review of the expanding clinico-radiological phenotypeRahul R Singh, Sagar Sedani, Ming Lim, et al.
Plos One|July 30, 2011
Prevalence and predictors of vitamin D insufficiency in children: a Great Britain population based studyMichael Absoud, Carole Cummins, Ming J Lim, et al.
Pageof 12

Showing results (1-10 of 120) with videos related to

Sort By:
Pageof 12
Developmental Medicine and Child Neurology|July 20, 2010
Mechanical ventilation in children with severe neurological impairmentShyam Mariguddi, Evangeline Wassmer
Journal of Child Neurology|December 17, 2008
Simultaneous peripheral and central demyelinationEvangeline Wassmer, William P Whitehouse
Journal of Child Neurology|January 15, 2008
Diagnostic yield of brain biopsies in children presenting to neurologySunita Venkateswaran, Cynthia Hawkins, Evangeline Wassmer
Biochimica Et Biophysica Acta. Biomembranes|September 12, 2021
Pathogenic antibodies to AQP4: Neuromyelitis optica spectrum disorder (NMOSD)Sukhvir K Wright, Evangeline Wassmer, Angela Vincent
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 4, 2025
Observational evidence of the treatment efficacy of IVIG as maintenance therapy for pediatric MOGADDaniel Griffiths-King, Evangeline Wassmer, Sukhvir K Wright
Archives of Disease in Childhood|January 25, 2020
Wilson disease in children and adolescentsMeranthi Fernando, Indra van Mourik, Evangeline Wassmer, et al.
Pediatric Neurology|July 25, 2003
Clinical spectrum associated with cerebellar hypoplasiaEvangeline Wassmer, Paul Davies, William P Whitehouse, et al.
Developmental Medicine and Child Neurology|February 12, 2011
Hereditary motor sensory neuropathy (type 1) presenting with transient and persistent central nervous system manifestations: a novel genetic mutationMichael Absoud, Louise Brueton, Rajat Gupta, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 20, 2014
RANBP2 mutation and acute necrotizing encephalopathy: 2 cases and a literature review of the expanding clinico-radiological phenotypeRahul R Singh, Sagar Sedani, Ming Lim, et al.
Plos One|July 30, 2011
Prevalence and predictors of vitamin D insufficiency in children: a Great Britain population based studyMichael Absoud, Carole Cummins, Ming J Lim, et al.
Pageof 12