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dc.contributor.authorVerbeek, Marcel M.
dc.contributor.authorTrislan-Noguero, Alba
dc.contributor.authorBorras, Eva
dc.contributor.authorMolero-Luis, Marta
dc.contributor.authorWassenberg, Tessa
dc.contributor.authorPeters, Tessa
dc.contributor.authorWillemsen, Michel
dc.contributor.authorOpladen, Thomas
dc.contributor.authorJeltsch, Kathrin
dc.contributor.authorPons, Roser
dc.contributor.authorThony, Beat
dc.contributor.authorHorvath, Gabriella
dc.contributor.authorYapici, Zuhal
dc.contributor.authorFriedman, Jennifer
dc.contributor.authorHyland, Keith
dc.contributor.authorAgosta, Guillermo E.
dc.contributor.authorLopez-Laso, Eduardo
dc.contributor.authorArtuch, Rafael
dc.contributor.authorSabido, Eduard
dc.contributor.authorGarcia-Cazorla, Angels
dc.date.accessioned2021-03-02T16:16:44Z
dc.date.available2021-03-02T16:16:44Z
dc.identifier.citationTrislan-Noguero A., Borras E., Molero-Luis M., Wassenberg T., Peters T., Verbeek M. M. , Willemsen M., Opladen T., Jeltsch K., Pons R., et al., "Novel Protein Biomarkers of Monoamine Metabolism Defects Correlate with Disease Severity", MOVEMENT DISORDERS, 2020
dc.identifier.issn0885-3185
dc.identifier.othervv_1032021
dc.identifier.otherav_710611c4-6464-4345-8d73-27d8edde1867
dc.identifier.urihttp://hdl.handle.net/20.500.12627/2755
dc.identifier.urihttps://doi.org/10.1002/mds.28362
dc.description.abstractBackground Genetic defects of monoamine neurotransmitters are rare neurological diseases amenable to treatment with variable response. They are major causes of early parkinsonism and other spectrum of movement disorders including dopa-responsive dystonia.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectKLİNİK NEUROLOJİ
dc.subjectNöroloji
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.titleNovel Protein Biomarkers of Monoamine Metabolism Defects Correlate with Disease Severity
dc.typeMakale
dc.relation.journalMOVEMENT DISORDERS
dc.contributor.departmentSt Joan de Deu Hosp , ,
dc.contributor.firstauthorID2359562


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