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dc.contributor.authorGRIGGS, RC
dc.contributor.authorTAWIL, R
dc.contributor.authorPENN, AS
dc.contributor.authorOZDEMIR, C
dc.contributor.authorPTACEK, LJ
dc.contributor.authorPAVLAKIS, SG
dc.contributor.authorDEVIVO, DC
dc.date.accessioned2021-03-03T17:35:05Z
dc.date.available2021-03-03T17:35:05Z
dc.date.issued1994
dc.identifier.citationTAWIL R., PTACEK L., PAVLAKIS S., DEVIVO D., PENN A., OZDEMIR C., GRIGGS R., "ANDERSENS-SYNDROME - POTASSIUM-SENSITIVE PERIODIC PARALYSIS, VENTRICULAR ECTOPY, AND DYSMORPHIC FEATURES", ANNALS OF NEUROLOGY, cilt.35, sa.3, ss.326-330, 1994
dc.identifier.issn0364-5134
dc.identifier.othervv_1032021
dc.identifier.otherav_4a68308c-fb07-4cda-bf33-8491f658c6fc
dc.identifier.urihttp://hdl.handle.net/20.500.12627/53462
dc.identifier.urihttps://doi.org/10.1002/ana.410350313
dc.description.abstractAndersen's syndrome is a clinically distinct form of potassium-sensitive periodic paralysis associated with cardiac dysrhythmias. The subtle nature of the cardiac and dysmorphic features may delay the recognition of this syndrome and its potentially lethal cardiac dysrhythmias. The genetic defect in Andersen's syndrome is not genetically linked to other forms of potassium-sensitive periodic paralysis and is probably distinct from the long QT syndrome locus.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.subjectKLİNİK NEUROLOJİ
dc.subjectTemel Bilimler
dc.titleANDERSENS-SYNDROME - POTASSIUM-SENSITIVE PERIODIC PARALYSIS, VENTRICULAR ECTOPY, AND DYSMORPHIC FEATURES
dc.typeMakale
dc.relation.journalANNALS OF NEUROLOGY
dc.contributor.department, ,
dc.identifier.volume35
dc.identifier.issue3
dc.identifier.startpage326
dc.identifier.endpage330
dc.contributor.firstauthorID115144


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