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Neurology. Genetics|January 30, 2023
Clinical Manifestation of Nebulin-Associated Nemaline MyopathyCristiane Araujo Martins Moreno, Mariana Cunha Artilheiro, Alulin Tacio Quadros Santos Monteiro Fonseca, et al.Annals of Neurology|January 16, 2026
Clot Composition Profiling in Large Vessel Occlusion Stroke Via RadiomicsAndres Gudino, Elena Sagues, Carlos Dier, et al.Brain : a Journal of Neurology|September 28, 2021
MLIP causes recessive myopathy with rhabdomyolysis, myalgia and baseline elevated serum creatine kinaseOsorio Lopes Abath Neto, Livija Medne, Sandra Donkervoort, et al.Science Translational Medicine|April 3, 2024
Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle diseaseSandra Donkervoort, Martijn van de Locht, Dario Ronchi, et al.Neuro-Oncology Advances|July 30, 2025
Molecular, histologic, and clinical characterization of methylation class pleomorphic xanthoastrocytoma: An analysis of 469 tumorsChristopher H Dampier, Niharika Shah, Kristyn Galbraith, et al.The EMBO Journal|November 14, 2018
Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegenerationVandana Shashi, Maria M Magiera, Dennis Klein, et al.Pageof 2