Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study.
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Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study. / Zittel, Simone; Kröger, Johan; van der Vegt, J P M; Siebner, H R; Brüggemann, N; Ramirez, A; Behrens, M I; Gerloff, Christian; Bäumer, Tobias; Klein, C; Münchau, Alexander.
in: PARKINSONISM RELAT D, Jahrgang 18, Nr. 5, 5, 2012, S. 590-594.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Motor pathway excitability in ATP13A2 mutation carriers: a transcranial magnetic stimulation study.
AU - Zittel, Simone
AU - Kröger, Johan
AU - van der Vegt, J P M
AU - Siebner, H R
AU - Brüggemann, N
AU - Ramirez, A
AU - Behrens, M I
AU - Gerloff, Christian
AU - Bäumer, Tobias
AU - Klein, C
AU - Münchau, Alexander
PY - 2012
Y1 - 2012
N2 - To describe excitability of motor pathways in Kufor-Rakeb syndrome (PARK9), an autosomal recessive nigro-striatal-pallidal-pyramidal neurodegeneration caused by a mutation in the ATP13A2 gene, using transcranial magnetic stimulation (TMS).
AB - To describe excitability of motor pathways in Kufor-Rakeb syndrome (PARK9), an autosomal recessive nigro-striatal-pallidal-pyramidal neurodegeneration caused by a mutation in the ATP13A2 gene, using transcranial magnetic stimulation (TMS).
M3 - SCORING: Journal article
VL - 18
SP - 590
EP - 594
JO - PARKINSONISM RELAT D
JF - PARKINSONISM RELAT D
SN - 1353-8020
IS - 5
M1 - 5
ER -