‘Leukodystrophy-like’ phenotype in children with myelin oligodendrocyte glycoprotein antibody-associated disease-Reference-Cited by-同舟云学术

‘Leukodystrophy-like’ phenotype in children with myelin oligodendrocyte glycoprotein antibody-associated disease

Published:2017-12-30 Issue:4 Volume:60 Page:417-423
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Hacohen Yael¹²^ORCID,Rossor Thomas³,Mankad Kshitij⁴,Chong Wk ‘Kling’⁴,Lux Andrew⁵,Wassmer Evangeline⁶,Lim Ming³,Barkhof Frederik⁷⁸⁹,Ciccarelli Olga¹⁹,Hemingway Cheryl²

Affiliation:

1. Department of Neuroinflammation; Queen Square MS Centre; UCL Institute of Neurology; London UK

2. Department of Paediatric Neurology; Great Ormond Street Hospital for Children; London UK

3. Children's Neurosciences; Evelina London Children's Hospital at Guy's and St Thomas’ NHS Foundation Trust; King's Health Partners Academic Health Science Centre; London UK

4. Paediatric Neuroradiology; Great Ormond Street Hospital; London UK

5. Department of Paediatric Neurology; University Hospitals Bristol; Bristol UK

6. Department of Paediatric Neurology; Birmingham Children's Hospital; Birmingham UK

7. Department of Radiology and Nuclear Medicine; VU University Medical Centre; Amsterdam the Netherlands

8. Institutes of Neurology and Biomedical Engineering, UCL; London UK

9. NIHR UCLH Biomedical Research Centre; London UK

Funder

National Institute for Health Research

University College London Hospitals Biomedical Research Centre (OC)

Action Medical Research

Multiple Sclerosis Society

DES society