Showing 221 - 240 results of 784 for search '"paraplegia"', query time: 0.08s Refine Results
  1. 221

    Serum Neurofilament Light Chain and Glial Fibrillary Acidic Protein as Biomarkers in Primary Progressive Multiple Sclerosis and Hereditary Spastic Paraplegia Type 4 by Christoph Kessler, Christoph Ruschil, Ahmed Abdelhak, Carlo Wilke, Aleksandra Maleska, Jens Kuhle, Markus Krumbholz, Markus C. Kowarik, Rebecca Schüle

    Published 2022-11-01
    “…In patients with slowly progressive spastic paraparesis, the differential diagnosis of primary progressive multiple sclerosis (PPMS) and hereditary spastic paraplegia (HSP) can be challenging. Serum neurofilament light chain (sNfL) and glial fibrillary acidic protein (sGFAP) are promising fluid biomarkers to support the diagnostic workup. …”
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    Feasibility, Usability, and Safety of ParaGym, an Intelligent Mobile Exercise App for Individuals With Paraplegia: Protocol for a Pilot Block-Randomized Controlled Trial by Janika Bolz, Adrian Löscher, Rainer Muhl, Andreas Badke, Hans-Georg Predel, Claudio Perret

    Published 2023-05-01
    “… BackgroundExercise is crucial for individuals with paraplegia to reduce the risk of secondary diseases and improve independence and quality of life. …”
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    EMPIEMA EPIDURAL RESULTANDO EM PARAPLEGIA - RELATO DE CASO EM HOSPITAL DE INFECTOLOGIA E DOENÇAS TROPICAIS DA AMAZÔNIA OCIDENTAL by Brenda K.S. Silva, Renata Gonçalves Santos, Juliana A.S. Barros, Fellipe R. Pereira, Maiara C.F. Soares, Marcelo S.S. Carvalho, Elza G.B. Pereira, Angela G.C.S. Melo, Angelo F. Almeida, Erica M.G. Pinheiro

    Published 2022-09-01
    “…Paciente procurou pronto socorro do Centro de Medicina Tropical do estado de Rondônia com quadro de dorsalgia e febre há 8 dias evoluindo agudamente com paraplegia e disfunção esfincteriana 1 dia antes da admissão. …”
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    Generation of an iPSC line from a patient with spastic paraplegia type 10 carrying a novel mutation in KIF5A gene by Serena Santangelo, Patrizia Bossolasco, Stefania Magri, Claudia Colombrita, Sabrina Invernizzi, Cinzia Gellera, Lorenzo Nanetti, Daniela Di Bella, Vincenzo Silani, Franco Taroni, Antonia Ratti

    Published 2023-02-01
    “…We generated an iPSC line from a patient with spastic paraplegia type 10 (SPG10) carrying the novel missense variant c.50G > A (p.R17Q) in the N-terminal motor domain of the kinesin family member 5A (KIF5A) gene.This patient-derived in vitro cell model will help to investigate the role of different KIF5A mutations in inducing neurodegeneration in spastic paraplegia and in other KIF5A-related disorders, including Charcot-Marie-Tooth type 2 (CMT2) and amyotrophic lateral sclerosis (ALS).…”
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