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Article

Lesser motor disability in adulthood: A ten-year follow-up of a dyskinetic patient with ADCY5 mutation

31 Jul 2019

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 31422281
DOI: 10.1016/j.jns.2019.07.001

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Related research

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Lesser motor disability in adulthood: A ten-year follow-up of a dyskinetic patient with ADCY5 mutationPMID 31422281Read ↗

ADCY5 gene mutation: a case report.Semantic proximity Read ↗

Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disordersSemantic proximity Read ↗

ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients.Semantic proximity Read ↗

Expanding the ADCY5 phenotype toward spastic paraparesisSemantic proximity Read ↗

ADCY5-related dyskinesia - case series with literature review.Semantic proximity Read ↗

Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability.Semantic proximity Read ↗

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesiasSemantic proximity Read ↗

An Update on the Phenotype, Genotype and Neurobiology of ADCY5-Related Disease.Semantic proximity Read ↗

ADCY5 Related Dyskinesia—A Rare MutationSemantic proximity Read ↗

ADCY5-related dyskinesia presenting as familial myoclonus-dystonia.Semantic proximity Read ↗

Depression and psychosis in ADCY5-related dyskinesia-part of the phenotypic spectrum?Semantic proximity Read ↗

De novo mutations in CLDN5: alternating hemiplegia of childhood or not?Semantic proximity Read ↗

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