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You searched for: Author/Creator Erdler, Marcus

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1. Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease. (1st December 2020)

2. Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease. (5th October 2021)

3. Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease. (5th October 2021)