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Mitochondrion|July 24, 2024
Early cardiac mechanics abnormalities in patients with mitochondrial diseasesRosa Lillo, Maria Chiara Meucci, Silvia Malara, et al.Neuromuscular Disorders : NMD|July 8, 2023
Clinical, neurophysiological and serological clues for the diagnosis of neuromyotonia and distinction from cramp-fasciculation syndromeGregorio Spagni, Anna Modoni, Guido Primiano, et al.Neuromuscular Disorders : NMD|November 25, 2011
A rapid immunohistochemical test to distinguish congenital myotonic dystrophy from X-linked myotubular myopathyCaroline A Sewry, Ros C M Quinlivan, Waney Squier, et al.Neuromuscular Disorders : NMD|March 30, 2024
Proteomic characterization of human LMNA-related congenital muscular dystrophy muscle cellsEmily C Storey, Ian Holt, Sharon Brown, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 11, 2017
Systematic assessment and characterization of chronic pain in multiple sclerosis patientsDiana Ferraro, Domenico Plantone, Franca Morselli, et al.Human Mutation|February 11, 2011
Characterization of MSH2 variants by endogenous gene modification in mouse embryonic stem cellsEva A L Wielders, Rob J Dekker, Ian Holt, et al.Cytoskeleton (Hoboken, N.J.)|June 17, 2014
Nesprin-1 and nesprin-2 regulate endothelial cell shape and migrationSamantha J King, Karolin Nowak, Narendra Suryavanshi, et al.Plos Genetics|May 14, 2009
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic miceStéphanie Tomé, Ian Holt, Winfried Edelmann, et al.Journal of Cell Science|June 5, 2003
Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivoIan Holt, Cecilia Ostlund, Colin L Stewart, et al.Brain Structure & Function|June 18, 2016
Monoclonal antibody Py recognizes neurofilament heavy chain and is a selective marker for large diameter neurons in the brainHeidi R Fuller, Lucia Marani, Ian Holt, et al.Pageof 12