Author

Brianna Blume

Observed institutions: Johns Hopkins University, University of Colorado Health, University of Colorado Anschutz

OpenAlex ID: A5067612910

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

2020 · Andrea Cortese, Yi Zhu, et al. · Nature Genetics · 176

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

2020 · David Adams, Michael Polydefkis, et al. · The Lancet Neurology · 159

Safety and efficacy of arimoclomol for inclusion body myositis: a multicentre, randomised, double-blind, placebo-controlled trial

2023 · Pedro M Machado, Michael P McDermott, et al. · The Lancet Neurology · 38

Assessing non-Mendelian inheritance in inherited axonopathies

2020 · Dana M. Bis-Brewer, Ziv Gan-Or, et al. · Genetics in Medicine · 26

Impact of Vutrisiran on Quality of Life and Physical Function in Patients with Hereditary Transthyretin-Mediated Amyloidosis with Polyneuropathy

2023 · Laura Obici, Senda Ajroud-Driss, et al. · Neurology and Therapy · 21

A Single Center Observational Case Series in Magnetic Resonance Imaging Features in Antibodyassociated Autoimmune Encephalitis (P2-1.004)

2026 · Jessica Woon, Tyler Borko, et al. · Neurology

Works count: 6

Citation count: 420

H-index: 5

I10-index: 5