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dc.contributor.authorSiciliano, G.
dc.contributor.authorBruno, C.
dc.contributor.authorWakelin, A.
dc.contributor.authorQuinlivan, R.
dc.contributor.authorVissing, J.
dc.contributor.authorMarti, R.
dc.contributor.authorDurmus, H.
dc.contributor.authorScalco, R.
dc.contributor.authorPinos, T.
dc.contributor.authorLucia, A.
dc.contributor.authorMartin, M.
dc.contributor.authorMartinuzzi, A.
dc.contributor.authorToscano, A.
dc.contributor.authorSan Millan, B.
dc.contributor.authorVoermans, N.
dc.contributor.authorLaforet, P.
dc.contributor.authorVorgerd, M.
dc.contributor.authorSacconi, S.
dc.contributor.authorKierdaszuk, B.
dc.date.accessioned2021-03-03T16:59:30Z
dc.date.available2021-03-03T16:59:30Z
dc.identifier.citationPinos T., Scalco R., Lucia A., Martin M., Martinuzzi A., Toscano A., San Millan B., Voermans N., Laforet P., Vorgerd M., et al., "EUROMAC: A European registry for patients with McArdle disease and other very rare muscle glycogenoses", 24th International Annual Congress of the World-Muscle-Society (WMS), Copenhagen, Danimarka, 1 - 05 Ekim 2019, cilt.29
dc.identifier.otherav_4753cf99-e13a-42be-b9cd-fa5acbbdb3d9
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/51515
dc.identifier.urihttps://doi.org/10.1016/j.nmd.2019.06.176
dc.language.isoeng
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp
dc.subjectTıp
dc.subjectTemel Bilimler
dc.subjectKlinik Tıp (MED)
dc.subjectNEUROSCIENCES
dc.subjectSinirbilim ve Davranış
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectYaşam Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectNöroloji
dc.titleEUROMAC: A European registry for patients with McArdle disease and other very rare muscle glycogenoses
dc.typeBildiri
dc.contributor.departmentMRC CNMD , ,
dc.identifier.volume29
dc.contributor.firstauthorID157633


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