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You searched for: Author/Creator Wassmer, Evangeline

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1. 'Leukodystrophy‐like' phenotype in children with myelin oligodendrocyte glycoprotein antibody‐associated disease. (30th December 2017)

3. A framework for measurement and harmonization of pediatric multiple sclerosis etiologic research studies: The Pediatric MS Tool-Kit. (July 2019)

5. Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort. Issue 4 (16th October 2013)

6. Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Issue 2 (8th June 2022)

7. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. (16th January 2015)

9. Clinical features, investigations, and outcomes of pediatric limbic encephalitis: A multicenter study. Issue 1 (11th January 2022)

10. Clinical trials of disease-modifying agents in pediatric MS: Opportunities, challenges, and recommendations from the IPMSSG. (28th May 2019)