Related Experiment Video

Updated: Jun 7, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
09:41

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis

Published on: July 19, 2019

Multiple sclerosis in association with Williams-Beuren syndrome

Eleni Papageorgiou, Annette Wacker, Thomas Nägele

    Journal of Paediatrics and Child Health
    |October 21, 2010
    PubMed
    Summary

    No abstract available in PubMed .

    More Related Videos

    Modeling Multiple Sclerosis in the Two Sexes: MOG35-55-Induced Experimental Autoimmune Encephalomyelitis
    05:44

    Modeling Multiple Sclerosis in the Two Sexes: MOG35-55-Induced Experimental Autoimmune Encephalomyelitis

    Published on: October 13, 2023

    Related Experiment Videos

    Last Updated: Jun 7, 2026

    Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
    09:41

    Comprehensive Autopsy Program for Individuals with Multiple Sclerosis

    Published on: July 19, 2019

    Modeling Multiple Sclerosis in the Two Sexes: MOG35-55-Induced Experimental Autoimmune Encephalomyelitis
    05:44

    Modeling Multiple Sclerosis in the Two Sexes: MOG35-55-Induced Experimental Autoimmune Encephalomyelitis

    Published on: October 13, 2023

    Related Concept Videos

    Multiple Sclerosis l: Introduction01:19

    Multiple Sclerosis l: Introduction

    Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
    Pleiotropy01:33

    Pleiotropy

    Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...

    Articles linked to this work by shared authors, journal, and citation graph.

    Prenatal Genetic Testing for Beckwith-Wiedemann Syndrome: Considerations, Challenges and Observations (A Real-World Study).

    Prenatal diagnosis·2026

    Ecological role of emergent properties in the chemodiversity landscape.

    Nature ecology & evolution·2026

    Integrating ionomes and metabolomes across organelles.

    Trends in plant science·2026

    PHR1 mediates rapid high light responses and acclimation to high photosynthetic activity.

    The Plant journal : for cell and molecular biology·2026

    Combining space use with diet data to investigate foraging tactics of black bears in response to the pulsed availability of migratory caribou calves.

    PloS one·2026

    Optical coherence tomography in pediatric ophthalmology: Insights into ocular development, diagnosis and management of eye diseases.

    Progress in retinal and eye research·2026

    Retinopathy of Prematurity Is Associated With Reduced Thalamic Volume and Impaired Neurodevelopment. A Cohort Study.

    Journal of paediatrics and child health·2026

    Screen Use, Child Development and Family Involvement in Children Aged 2-7 Years: A Systematic Review.

    Journal of paediatrics and child health·2026

    Optimising Asparaginase Use and Managing Hypersensitivity in Australasia-A Clinical Practice Guideline From the Australian and New Zealand Children's Haematology/Oncology Group.

    Journal of paediatrics and child health·2026

    Ganciclovir Improves Transplant-Free Liver Survival in Children With Biliary Atresia and Concurrent Cytomegaloviral Infection: A Pilot Study.

    Journal of paediatrics and child health·2026

    HOMEFREE: Scaling-Up Evidence-Based Guidelines for IV-to-Oral Antibiotic Switch in Hospitalised Children, an Implementation Study Protocol.

    Journal of paediatrics and child health·2026

    The Performance of the STRONGkids Nutrition Screening Tool Following Nurse Training in a Tertiary Care Setting.

    Journal of paediatrics and child health·2026

    Optimizing teduglutide treatment regimens in children with short bowel syndrome.

    Frontiers in pediatrics·2026

    Micronutrients and ICU-Acquired Weakness: A Narrative Review.

    Journal of clinical medicine·2026

    The Use of Peripheral Parenteral Nutrition in Hospitalized Patients: A Clinical Case Series.

    Healthcare (Basel, Switzerland)·2026

    Integrated Analysis of Zinc, Copper, and Magnesium Homeostasis in Pediatric Idiopathic Nephrotic Syndrome: A Prospective Cohort Study with Serial Clinical Evaluation.

    Nutrients·2026

    Severe Vitamin D Deficiency as a Trigger for Metabolic Seizures in Infancy: A Case Series and a Comprehensive Review of the Literature.

    Nutrients·2026

    Assessment of Bone Mass and Fracture Risk Using Trabecular Bone Score in Children with Autoimmune Gastrointestinal Diseases.

    Nutrients·2026
    See all related articles
    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
    Jove
    Visualize
    Contact Us