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Brain : a Journal of Neurology|June 9, 2025
Charcot-Marie-Tooth disease type 1E: clinical natural history and molecular impact of PMP22 variantsKailee S Ward, Christopher P Ptak, Natalya Pashkova, et al.EJNMMI Radiopharmacy and Chemistry|March 26, 2026
Highlight selection of radiochemistry and radiopharmacy developments by editorial boardOliver C Kiss, Ivan Penuelas, Ana Rey, et al.Science (New York, N.Y.)|September 13, 2021
The integrated stress response contributes to tRNA synthetase-associated peripheral neuropathyE L Spaulding, T J Hines, P Bais, et al.Neurology|September 8, 2021
Association Between Body Mass Index and Disability in Children With Charcot-Marie-Tooth DiseaseGabrielle A Donlevy, Sarah P Garnett, Kayla M D Cornett, et al.Nature Genetics|March 31, 2019
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Roberto Simone, Roisin Sullivan, et al.Journal for Immunotherapy of Cancer|July 1, 2026
ENPP3 CAR T cells combined with CD206 modulation suppress adrenocortical carcinomaReona Okada, Arnulfo Mendoza, Darryl Nousome, et al.Nature Genetics|April 28, 2019
Author Correction: Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxiaAndrea Cortese, Roberto Simone, Roisin Sullivan, et al.Brain Communications|March 10, 2023
Investigating genotype-phenotype relationship of extreme neuropathic pain disorders in a UK national cohortAndreas C Themistocleous, Georgios Baskozos, Iulia Blesneac, et al.American Journal of Human Genetics|May 14, 2013
Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegiaEmily C Oates, Alexander M Rossor, Majid Hafezparast, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2019
Expanding the spectrum of genes responsible for hereditary motor neuropathiesStefano C Previtali, Edward Zhao, Dejan Lazarevic, et al.Pageof 163