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You searched for: Author/Creator Kaindl, Angela

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

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

3. Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability. Issue 11 (5th October 2018)

4. Phenotype variability of infantile-onset multisystem neurologic, endocrine, and pancreatic disease IMNEPD. Issue 1 (December 2016)

5. The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series. (15th September 2020)