Published Data Registry

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TitleAuthorsJournalPublication year
DOI
PMID
Genetic analysis for a shared biological basis between migraine and coronary artery disease.(Open Access) Winsvold BS, Nelson CP, (...), Palotie ANeurology. Genetics2015
Restless legs syndrome-current therapies and management of augmentation.Trenkwalder C, Winkelmann J, Inoue Y, Paulus WNature reviews. Neurology2015
Response to Letter Regarding Article, "Cysteine-Sparing CADASIL Mutations in NOTCH3 Show Proaggregatory Properties In Vitro".(Open Access) Wollenweber FA, Haffner C, Duering MStroke2015
TOR1A, THAP1, and GNAL mutational screening in Austrian patients with primary isolated dystonia.Zech M, Boesch S, Sycha T, Mueller J, Poewe W, Winkelmann JMovement disorders : official journal of the Movement Disorder Society2015
Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.(Open Access) Adib-Samii P, Devan W, (...), Markus HSStroke2015
Large-scale TUBB4A mutational screening in isolated dystonia and controls.Zech M, Boesch S, (...), Winkelmann JParkinsonism & related disorders2015
Deficiency of the stroke relevant HDAC9 gene attenuates atherosclerosis in accord with allele-specific effects at 7p21.1.(Open Access) Azghandi S, Prell C, (...), Dichgans MStroke2015
Reply to letter: Novel compound heterozygous mutations in PRKRA cause pure dystonia.Zech M, Castrop F, Haslinger B, Winkelmann JMovement disorders : official journal of the Movement Disorder Society2015
Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystonia.(Open Access) Zech M, Lam DD, (...), Winkelmann JAmerican journal of human genetics2015
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.(Open Access) Debette S, Kamatani Y, (...), Dallongeville JNature genetics2015