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dc.contributor.authorCUTTINI, Marina
dc.contributor.authorParman, Yesim
dc.contributor.authorOZDEMIR, Coskun
dc.contributor.authorDeymeer, Feza
dc.contributor.authorBaslo, Mehmet Barış
dc.contributor.authorSERDAROGLU, Piraye
dc.date.accessioned2021-03-05T12:02:14Z
dc.date.available2021-03-05T12:02:14Z
dc.date.issued2006
dc.identifier.citationBaslo M. B. , Deymeer F., SERDAROGLU P., Parman Y., OZDEMIR C., CUTTINI M., "Decrement pattern in Lambert-Eaton myasthenic syndrome is different from myasthenia gravis", NEUROMUSCULAR DISORDERS, cilt.16, ss.454-458, 2006
dc.identifier.issn0960-8966
dc.identifier.othervv_1032021
dc.identifier.otherav_ab1d1857-1fac-45e0-be20-2e1bbfba9760
dc.identifier.urihttp://hdl.handle.net/20.500.12627/114255
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2006.05.009
dc.description.abstractThe decrement pattern at low rates of repetitive nerve stimulation in myasthenia gravis (MG) is characterized by a decrease of compound muscle action potential size within the first 4-5 responses. With subsequent stimuli, compound muscle action potential size either increases or does not change. Following an observation that the pattern of decrement might be different in patients with Lambert-Eaton myasthenic syndrome (LEMS), we retrospectively studied traces from eight LEMS patients and 14 patients with seropositive generalized MG, calculating decrement percent from first to fourth and from first to ninth compound muscle action potential. In the LEMS patients, compound muscle action potential amplitude decreased progressively from first to ninth stimulus at 2, 3 or 5 Hz in all traces but one. In contrast, MG patients demonstrated the expected improvement after the initial decrement in all traces except one. In the evaluation of patients suspected of having myasthenia gravis, the finding of progressive decrement pattern at low rates of repetitive nerve stimulation may alert the electromyographer to the possibility of Lambert-Eaton syndrome and prompt the performance of further electrodiagnostic tests. (C) 2006 Published by Elsevier B.V.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectYaşam Bilimleri
dc.subjectTemel Bilimler
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectSinirbilim ve Davranış
dc.subjectNEUROSCIENCES
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleDecrement pattern in Lambert-Eaton myasthenic syndrome is different from myasthenia gravis
dc.typeMakale
dc.relation.journalNEUROMUSCULAR DISORDERS
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume16
dc.identifier.issue7
dc.identifier.startpage454
dc.identifier.endpage458
dc.contributor.firstauthorID24595


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