يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"Muscular Dystrophies"', وقت الاستعلام: 1.00s تنقيح النتائج
  1. 1
    دورية أكاديمية
    A wearable device for breathing frequency monitoring: A pilot study on patients with muscular dystrophy

    المؤلفون: Cesareo A., Nido S. A., Biffi E., Gandossini S., D'angelo M. G., Aliverti A.

    المساهمون: Cesareo, A., Nido, S. A., Biffi, E., Gandossini, S., D'Angelo, M. G., Aliverti, A.

    مصطلحات موضوعية: Breathing monitoring, Breathing rate variation, Neuromuscular patients, Wearable IMUs, Humans, Monitoring, Physiologic, Pilot Projects, Respiration, Muscular Dystrophies, Wearable Electronic Devices

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32961986; info:eu-repo/semantics/altIdentifier/wos/WOS:000581333900001; volume:20; issue:18; firstpage:1; lastpage:19; numberofpages:19; journal:SENSORS; http://hdl.handle.net/11311/1170113Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85091105931

    الإتاحة: https://doi.org/10.3390/s20185346Test
    http://hdl.handle.net/11311/1170113Test

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  2. 2
    دورية أكاديمية
    Over three decades of natural history of limb girdle muscular dystrophy type R1/2A and R2/2B: Mathematical modelling of a multifactorial study

    المؤلفون: LoMauro A., Gandossini S., Russo A., Diella E., Pistininzi C., Marchi E., Pascuzzo R., Vantini S., Aliverti A., D'Angelo M. G.

    المساهمون: Lomauro, A., Gandossini, S., Russo, A., Diella, E., Pistininzi, C., Marchi, E., Pascuzzo, R., Vantini, S., Aliverti, A., D'Angelo, M. G.

    مصطلحات موضوعية: LGMD2A, LGMD2B, LGMDR1, LGMDR2, Mathematical modelling, Natural history, Adult, Disease Progression, Female, Forced Expiratory Volume, Humans, Male, Middle Aged, Motor Activity, Muscle Strength, Muscle, Skeletal, Muscular Dystrophies, Limb-Girdle, Phenotype, Retrospective Studies, Vital Capacity, Models, Theoretical

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33836912; info:eu-repo/semantics/altIdentifier/wos/WOS:000663041300002; volume:31; issue:6; firstpage:489; lastpage:497; numberofpages:9; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/11311/1205168Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85103938806

    الإتاحة: https://doi.org/10.1016/j.nmd.2021.02.018Test
    http://hdl.handle.net/11311/1205168Test

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  3. 3
    دورية أكاديمية
    Autologous intramuscular transplantation of engineered satellite cells induces exosome-mediated systemic expression of Fukutin-related protein and rescues disease phenotype in a murine model of limb-girdle muscular dystrophy type 2I

    المؤلفون: Frattini, Paola, Villa, Chiara, Santis, Francesca De, Meregalli, Mirella, Belicchi, Marzia, Erratico, Silvia, Bella, Pamela, Raimondi, Manuela Teresa, Lu, Qilong, Torrente, Yvan

    المساهمون: Frattini, Paola, Villa, Chiara, Santis, Francesca De, Meregalli, Mirella, Belicchi, Marzia, Erratico, Silvia, Bella, Pamela, Raimondi, Manuela Teresa, Lu, Qilong, Torrente, Yvan

    مصطلحات موضوعية: Animal, Disease Models, Dystroglycan, Exosome, Glycosylation, Glycosyltransferase, Human, Mice, Transgenic, Muscle, Skeletal, Muscular Dystrophies, Limb-Girdle, Myoblast, Protein, Satellite Cells, Skeletal Muscle, Molecular Biology, Genetic, Genetics (clinical)

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28666318; info:eu-repo/semantics/altIdentifier/wos/WOS:000411069400003; volume:26; issue:19; firstpage:3682; lastpage:3698; numberofpages:17; journal:HUMAN MOLECULAR GENETICS; http://hdl.handle.net/11311/1045627Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85030689762; http://hmg.oxfordjournals.orgTest/

    الإتاحة: https://doi.org/10.1093/hmg/ddx252Test
    http://hdl.handle.net/11311/1045627Test
    http://hmg.oxfordjournals.orgTest/

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