These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. Camargos S; Scholz S; Simón-Sánchez J; Paisán-Ruiz C; Lewis P; Hernandez D; Ding J; Gibbs JR; Cookson MR; Bras J; Guerreiro R; Oliveira CR; Lees A; Hardy J; Cardoso F; Singleton AB Lancet Neurol; 2008 Mar; 7(3):207-15. PubMed ID: 18243799 [TBL] [Abstract][Full Text] [Related]
24. Characterization of PLA2G6 as a locus for dystonia-parkinsonism. Paisan-Ruiz C; Bhatia KP; Li A; Hernandez D; Davis M; Wood NW; Hardy J; Houlden H; Singleton A; Schneider SA Ann Neurol; 2009 Jan; 65(1):19-23. PubMed ID: 18570303 [TBL] [Abstract][Full Text] [Related]
25. Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation. Méneret A; Mignot C; An I; Habert MO; Jacquette A; Vidailhet M; Bienvenu T; Roze E Mov Disord; 2012 Jan; 27(1):160-1. PubMed ID: 21953941 [No Abstract] [Full Text] [Related]
26. Rare causes of dystonia-parkinsonism with cognitive impairment, behavioral abnormalities, and voiceless whispering stereotypies: Describing the long-term evolution of the neurological phenotype in a patient with the PSEN2 Ile149Thr variant. Romito LM; Prioni S; Braccia A; Catania M; Elia AE; Dondi F; Lucchini S; Bertagna F; Piacentini SHMJ; Eleopra R; Di Fede G J Neurol Sci; 2023 Nov; 454():120846. PubMed ID: 38236755 [No Abstract] [Full Text] [Related]
27. Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family. Kuo MC; Lin HI; Lin CH Parkinsonism Relat Disord; 2019 May; 62():236-238. PubMed ID: 30692049 [No Abstract] [Full Text] [Related]
28. Pharmacochaperoning in a Asjad HMM; Kasture A; El-Kasaby A; Sackel M; Hummel T; Freissmuth M; Sucic S J Biol Chem; 2017 Nov; 292(47):19250-19265. PubMed ID: 28972153 [TBL] [Abstract][Full Text] [Related]
29. Cognitive impairment in rapid-onset dystonia-parkinsonism. Cook JF; Hill DF; Snively BM; Boggs N; Suerken CK; Haq I; Stacy M; McCall WV; Ozelius LJ; Sweadner KJ; Brashear A Mov Disord; 2014 Mar; 29(3):344-50. PubMed ID: 24436111 [TBL] [Abstract][Full Text] [Related]
31. ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism. Lee JY; Gollamudi S; Ozelius LJ; Kim JY; Jeon BS Mov Disord; 2007 Sep; 22(12):1808-9. PubMed ID: 17595045 [TBL] [Abstract][Full Text] [Related]
32. Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood. Ng J; Zhen J; Meyer E; Erreger K; Li Y; Kakar N; Ahmad J; Thiele H; Kubisch C; Rider NL; Morton DH; Strauss KA; Puffenberger EG; D'Agnano D; Anikster Y; Carducci C; Hyland K; Rotstein M; Leuzzi V; Borck G; Reith ME; Kurian MA Brain; 2014 Apr; 137(Pt 4):1107-19. PubMed ID: 24613933 [TBL] [Abstract][Full Text] [Related]
33. Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3). Németh AH; Nolte D; Dunne E; Niemann S; Kostrzewa M; Peters U; Fraser E; Bochukova E; Butler R; Brown J; Cox RD; Levy ER; Ropers HH; Monaco AP; Müller U Genomics; 1999 Sep; 60(3):320-9. PubMed ID: 10493831 [TBL] [Abstract][Full Text] [Related]