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Dehydroepiandrosterone sulphate as a putative protective factor against tardive dyskinesia.Academic Article Why?
DNAJC12-associated developmental delay, movement disorder, and mild hyperphenylalaninemia identified by whole-exome sequencing re-analysis.Academic Article Why?
Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.Academic Article Why?
N-methyl-D-aspartate receptor antibody-associated movement disorder without encephalopathy.Academic Article Why?
Prevalence of inherited neurotransmitter disorders in patients with movement disorders and epilepsy: a retrospective cohort study.Academic Article Why?
Psychogenic movement disorders in children: characteristics and predictors of outcome.Academic Article Why?
Acetylcholine receptor antibodies in tardive dyskinesia.Academic Article Why?
Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophrenia.Academic Article Why?
Effect of L-arginine infusion on airway NO in cystic fibrosis and primary ciliary dyskinesia syndrome.Academic Article Why?
Genetic landscape of pediatric movement disorders and management implications.Academic Article Why?
Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy.Academic Article Why?
SIL1-related Marinesco-Sjoegren syndrome (MSS) with associated motor neuronopathy and bradykinetic movement disorder.Academic Article Why?
Synaptic UNC13A protein variant causes increased neurotransmission and dyskinetic movement disorder.Academic Article Why?
Tardive dyskinesia and DRD3, HTR2A and HTR2C gene polymorphisms in Russian psychiatric inpatients from Siberia.Academic Article Why?
Movement DisordersConcept Why?
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