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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 24, 2025. (Total: 235644Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Movement Disorders and COMT[original query]
Candidate gene-based association study of antipsychotic-induced movement disorders in long-stay psychiatric patients: a prospective study.
PloS one 2012 7 (5): e36561.
Bakker P Roberto, Bakker Egbert, Amin Najaf, van Duijn Cornelia M, van Os Jim, van Harten Peter
Polymorphisms of COMT (c.649G>A), MAO-A (c.1460C>T), NET (c.1287G>A) Genes and the Level of Catecholamines, Serotonin in Patients with Parkinson's Disease.
DNA and cell biology 2017 Apr .
Florczak-Wyspianska Jolanta, Rozycka Agata, Wolny Lukasz, Lianeri Margarita, Kozubski Wojciech, Dorszewska Jolan
Functional monoamine oxidase B gene intron 13 polymorphism predicts putaminal dopamine turnover in de novo Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2018 Sep .
Löhle Matthias, Mangone Graziella, Wolz Martin, Beuthien-Baumann Bettina, Oehme Liane, van den Hoff Jörg, Kotzerke Jörg, Reichmann Heinz, Corvol Jean-Christophe, Storch Alexand
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