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5. Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5. Chen YZ; Matsushita MM; Robertson P; Rieder M; Girirajan S; Antonacci F; Lipe H; Eichler EE; Nickerson DA; Bird TD; Raskind WH Arch Neurol; 2012 May; 69(5):630-5. PubMed ID: 22782511 [TBL] [Abstract][Full Text] [Related]
6. A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia. Carapito R; Paul N; Untrau M; Le Gentil M; Ott L; Alsaleh G; Jochem P; Radosavljevic M; Le Caignec C; David A; Damier P; Isidor B; Bahram S Mov Disord; 2015 Mar; 30(3):423-7. PubMed ID: 25545163 [TBL] [Abstract][Full Text] [Related]
7. Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability. Okamoto N; Miya F; Kitai Y; Tsunoda T; Kato M; Saitoh S; Kanemura Y; Kosaki K Neurol Sci; 2021 Jul; 42(7):2975-2978. PubMed ID: 33704598 [TBL] [Abstract][Full Text] [Related]
8. Treatment of ADCY5-Associated Dystonia, Chorea, and Hyperkinetic Disorders With Deep Brain Stimulation: A Multicenter Case Series. Dy ME; Chang FC; Jesus SD; Anselm I; Mahant N; Zeilman P; Rodan LH; Foote KD; Tan WH; Eskandar E; Sharma N; Okun MS; Fung VS; Waugh JL J Child Neurol; 2016 Jul; 31(8):1027-35. PubMed ID: 27052971 [TBL] [Abstract][Full Text] [Related]
9. Kamate M; Mittal N Neurol India; 2018; 66(Supplement):S141-S142. PubMed ID: 29503338 [No Abstract] [Full Text] [Related]
10. An Update on the Phenotype, Genotype and Neurobiology of ADCY5-Related Disease. Ferrini A; Steel D; Barwick K; Kurian MA Mov Disord; 2021 May; 36(5):1104-1114. PubMed ID: 33934385 [TBL] [Abstract][Full Text] [Related]
11. ADCY5-related movement disorders: Frequency, disease course and phenotypic variability in a cohort of paediatric patients. Carecchio M; Mencacci NE; Iodice A; Pons R; Panteghini C; Zorzi G; Zibordi F; Bonakis A; Dinopoulos A; Jankovic J; Stefanis L; Bhatia KP; Monti V; R'Bibo L; Veneziano L; Garavaglia B; Fusco C; Wood N; Stamelou M; Nardocci N Parkinsonism Relat Disord; 2017 Aug; 41():37-43. PubMed ID: 28511835 [TBL] [Abstract][Full Text] [Related]
12. Depression and psychosis in ADCY5-related dyskinesia-part of the phenotypic spectrum? Vijiaratnam N; Newby R; Kempster PA J Clin Neurosci; 2018 Nov; 57():167-168. PubMed ID: 30172639 [TBL] [Abstract][Full Text] [Related]
13. Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders. Bohlega SA; Abou-Al-Shaar H; AlDakheel A; Alajlan H; Bohlega BS; Meyer BF; Monies D; Cupler EJ; Al-Saif AM Parkinsonism Relat Disord; 2019 Jul; 64():145-149. PubMed ID: 30975617 [TBL] [Abstract][Full Text] [Related]
14. Phenotypic insights into ADCY5-associated disease. Chang FC; Westenberger A; Dale RC; Smith M; Pall HS; Perez-Dueñas B; Grattan-Smith P; Ouvrier RA; Mahant N; Hanna BC; Hunter M; Lawson JA; Max C; Sachdev R; Meyer E; Crimmins D; Pryor D; Morris JG; Münchau A; Grozeva D; Carss KJ; Raymond L; Kurian MA; Klein C; Fung VS Mov Disord; 2016 Jul; 31(7):1033-40. PubMed ID: 27061943 [TBL] [Abstract][Full Text] [Related]
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17. ADCY5 identified as a novel cause of benign hereditary chorea. Raj Kumar K; Fung VS Mov Disord; 2015 Nov; 30(13):1726. PubMed ID: 26408352 [No Abstract] [Full Text] [Related]
18. Efficacy of Caffeine in ADCY5-Related Dyskinesia: A Retrospective Study. Méneret A; Mohammad SS; Cif L; Doummar D; DeGusmao C; Anheim M; Barth M; Damier P; Demonceau N; Friedman J; Gallea C; Gras D; Gurgel-Giannetti J; Innes EA; Necpál J; Riant F; Sagnes S; Sarret C; Seliverstov Y; Paramanandam V; Shetty K; Tranchant C; Doulazmi M; Vidailhet M; Pringsheim T; Roze E Mov Disord; 2022 Jun; 37(6):1294-1298. PubMed ID: 35384065 [TBL] [Abstract][Full Text] [Related]
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