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Circulation. Cardiovascular Imaging|February 20, 2024
Closing the Last Mile Gap in Access to Multimodality Imaging in Rural Settings: Design of the Imaging Core of the Risk Underlying Rural Areas Longitudinal StudyHooman Fazlalizadeh, Muhammad Shahzeb Khan, Ervin R Fox, et al.
Journal of Neurology|November 16, 2019
Analysis of autonomic outcomes in APOLLO, a phase III trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosisAlejandra González-Duarte, John L Berk, Dianna Quan, et al.
JACC. Cardiovascular Interventions|October 30, 2023
1-Year Outcomes Following Transfemoral Transseptal Transcatheter Mitral Valve Replacement: Intrepid TMVR Early Feasibility Study ResultsFiras Zahr, Howard K Song, Scott Chadderdon, et al.
Journal of Neurology|February 8, 2020
Correction to: Analysis of autonomic outcomes in APOLLO, a phase III trial of the RNAi therapeutic patisiran in patients with hereditary transthyretin-mediated amyloidosisAlejandra González-Duarte, John L Berk, Dianna Quan, et al.
European Journal of Neurology|August 15, 2022
Anti-disialosyl-immunoglobulin M chronic autoimmune neuropathies: a nationwide multicenter retrospective studyClaire Peillet, David Adams, Shahram Attarian, et al.
Brain Communications|October 15, 2021
Neurological complications induced by immune checkpoint inhibitors: a comprehensive descriptive case-series unravelling high risk of long-term sequelaeLéo Plaçais, Jean-Marie Michot, Stéphane Champiat, et al.
Annals of Clinical and Translational Neurology|January 19, 2019
Novel pathogenic COX20 variants causing dysarthria, ataxia, and sensory neuropathyMaria G Otero, Emmanuelle Tiongson, Frank Diaz, et al.
European Journal of Neurology|June 1, 2021
Charcot-Marie-Tooth disease misdiagnosed as chronic inflammatory demyelinating polyradiculoneuropathy: An international multicentric retrospective studyFabien Hauw, Guillaume Fargeot, David Adams, et al.
Human Genetics|March 7, 2024
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomaliesDaniel Brooks, Elizabeth Burke, Sukyeong Lee, et al.
Neuromuscular Disorders : NMD|March 5, 2013
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)Tyler Mark Pierson, Thomas Markello, John Accardi, et al.
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