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Brain Communications|December 8, 2025
Serum neuronal, glial and mitochondrial markers in autosomal dominant optic atrophy and Leber hereditary optic neuropathyAlessandra Rufa, Domenico Plantone, Alessia Bargagli, et al.Journal of Molecular Histology|June 27, 2007
Endosomal location of dopamine receptors in neuronal cell cytoplasmElizabeth C Wolstencroft, Goran Simic, Nguyen thi Man, et al.Frontiers in Neurology|July 3, 2019
Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case ReportClaudia Strafella, Giulia Campoli, Rosaria Maria Galota, et al.Clinical Genetics|December 2, 2023
Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian familiesClaudia Strafella, Luca Colantoni, Domenica Megalizzi, et al.Journal of Cellular Biochemistry|June 18, 2005
Characterisation of the transcription factor, SIX5, using a new panel of monoclonal antibodiesY Chan N Pham, Nguyen thi Man, Ian Holt, et al.Plos One|April 11, 2014
Nesprins: tissue-specific expression of epsilon and other short isoformsNguyen Thuy Duong, Glenn E Morris, Le Thanh Lam, et al.European Journal of Neurology|October 28, 2021
Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of AtaxiaValentina Damato, Claudia Papi, Gregorio Spagni, et al.The Journal of Physiology|May 5, 2025
Pathogenic TNNT1 variants are associated with aberrant thin filament compliance and myofibre hyper-contractilityJenni Laitila, Christopher T A Lewis, Anthony L Hessel, et al.Scientific Reports|October 26, 2018
Two alternatively-spliced human nebulin isoforms with either exon 143 or exon 144 and their developmental regulationLe Thanh Lam, Ian Holt, Jenni Laitila, et al.European Journal of Neurology|September 19, 2023
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis?Angela Romano, Guido Primiano, Giovanni Antonini, et al.Pageof 12