Jean-Martin Charcot's 1883 lectures on aphasia at the Salpêtrière Hospital were seen as the starting point for the development of a psychology in the work of the famous neurologist. In his lectures, Charcot set out a theory of language function at the cerebral level, distinguishing between the different centers involved in speech production and those necessary for reading. His lectures, which also postulated the independence of ideas from words, were to resonate beyond aphasia specialists, and particularly with alienists. To document this dimension of the reception of neurology in the field of psychiatry, this article refers to Jules Séglas's synthesis on , published in 1892, which summarized the knowledge acquired during the nineteenth century about modifications of expression in madness and whose original ideas were to mark the psychiatric semiology of the early-twentieth century. The analysis details how Séglas cited and adapted Charcot's conceptions to explain the production of incomprehensible speech in idiocy and the formation of hallucinations, thus contributing to the spread of the neurologist's model among his fellow alienists.
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http://dx.doi.org/10.1080/0964704X.2024.2365573 | DOI Listing |
Mult Scler
December 2024
Queen Square MS Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.
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View Article and Find Full Text PDFEur J Immunol
December 2024
Laboratory of Experimental Hematology, Vaccine and Infections Disease Institute (VAXINFECTIO), Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
Genetic engineering of regulatory T cells (Tregs) presents a promising avenue for advancing immunotherapeutic strategies, particularly in autoimmune diseases and transplantation. This study explores the modification of Tregs via mRNA electroporation, investigating the influence of T-cell activation status on transfection efficiency, phenotype, and functionality. For this CD45RA Tregs were isolated, expanded, and modified to overexpress brain-derived neurotrophic factor (BDNF).
View Article and Find Full Text PDFAnn Clin Transl Neurol
December 2024
NextGen Precision Health, University of Missouri, Columbia, Missouri, USA.
Objective: Charcot-Marie Tooth (CMT) is a hereditary neuropathy characterized by muscle weakness and fatigue with no approved therapies. Preclinical studies implicate neuromuscular junction (NMJ) transmission deficits in muscle dysfunction in CMT. This study aimed to evaluate NMJ function in patients with CMT types 1 and 2, and to determine whether enhancing NMJ transmission can improve muscle function in preclinical CMT models.
View Article and Find Full Text PDFGenet Med Open
March 2024
Medical Genetics Division, Department of Pediatrics, CHU Sainte-Justine, Montreal, QC, Canada.
Purpose: Biallelic variants in or are associated with Yunis-Varón syndrome (YVS), which is characterized by multisystem involvement including skeletal findings, craniofacial dysmorphisms and central nervous system anomalies. Pathogenic variants in those same genes have also been associated with a predominantly neurological phenotype and with nonsyndromic conditions, such as Charcot-Marie-Tooth disease and amyotrophic lateral sclerosis. By describing 5 new cases of -associated YVS and reviewing the literature, we better delineate the clinical phenotype associated with loss of function of those genes.
View Article and Find Full Text PDFNeurobiol Dis
December 2024
National Tsing Hua University, Institute of Molecular and Cellular Biology, Department of Life Science, Hsinchu 30013, Taiwan, ROC. Electronic address:
Kinesin-3 KIF1A (UNC-104 in C. elegans) is the major axonal transporter of synaptic vesicles and mutations in this molecular motor are linked to KIF1A-associated neurological disorders (KAND), encompassing Charcot-Marie-Tooth disease, amyotrophic lateral sclerosis and hereditary spastic paraplegia. UNC-104 binds to lipid bilayers of synaptic vesicles via its C-terminal PH (pleckstrin homology) domain.
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