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Article
SLC12A2 mutations cause NKCC1 deficiency with encephalopathy and impaired secretory epithelia
Tommy Stödberg, Måns Magnusson, Nicole Lesko, et al.

Neurology Genetics July 02, 2020
Resident & Fellow Section
Pearls & Oy-sters: Focal hypocalcemic seizures secondary to severe vitamin D deficiency/rickets
Rita Monni, Francesca Beccaria, Flavio Boscaini, et al.

Neurology June 16, 2020
Resident & Fellow Section
Clinical Reasoning: A 58-year-old woman presents with progressive memory deficits, odd behavior, and falls
Tara C. Carlisle, Kristin M. Galetta, Scott M. McGinnis, et al.

Neurology January 20, 2020
Case
Accelerated mineralization as a mimic of hemorrhagic conversion
Shivani Ghoshal, Nada El Husseini

Neurology: Clinical Practice October 30, 2019