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1. AB1168 SIGLEC1/CD169 IS A SENSITIVE MARKER FOR MONOGENIC INTERFERONOPATHIES. (June 2019)

3. BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood. Issue 9 (9th June 2016)

4. Clinical and imaging features of children with autoimmune encephalitis and MOG antibodies. Issue 4 (July 2020)

5. Clinical and Magnetic Resonance Imaging Outcome Predictors in Pediatric Anti–N‐Methyl‐D‐Aspartate Receptor Encephalitis. Issue 1 (29th May 2020)

7. De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy. Issue 3 (28th November 2018)