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7. A new mutation of GCH1 in triplets family with dopa-responsive dystonia. Tachi N; Takahashi S; Jo M; Shinoda M Eur J Neurol; 2011 Sep; 18(9):1191-3. PubMed ID: 21834904 [TBL] [Abstract][Full Text] [Related]
8. Child Neurology: A young child with an undiagnosed case of dystonia responsive to l-dopa. Trau SP; Gallentine WB; Mikati MA Neurology; 2020 Feb; 94(7):326-328. PubMed ID: 32015175 [TBL] [Abstract][Full Text] [Related]
9. A case of late-onset Segawa syndrome (autosomal dominant dopa-responsive dystonia) with a novel mutation of the GTP-cyclohydrase I (GCH1) gene. Furuya H; Murai H; Takasugi K; Ohyagi Y; Urano F; Kishi T; Ichinose H; Kira J Clin Neurol Neurosurg; 2006 Dec; 108(8):784-6. PubMed ID: 16289769 [TBL] [Abstract][Full Text] [Related]
10. A novel missense mutation of the GTP cyclohydrolase I gene in a Korean family with hereditary progressive dystonia/dopa-responsive dystonia. Kang JH; Kang SY; Kang HK; Koh YS; Im JH; Lee MC Brain Dev; 2004 Aug; 26(5):287-91. PubMed ID: 15165667 [TBL] [Abstract][Full Text] [Related]
11. A case of secondary dystonia responding to levodopa. Bernard G; Vanasse M; Chouinard S J Child Neurol; 2010 Jun; 25(6):780-1. PubMed ID: 19808991 [TBL] [Abstract][Full Text] [Related]
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13. Segawa's disease: dopa-responsive dystonia. Gordon N Int J Clin Pract; 2008 Jun; 62(6):943-6. PubMed ID: 17971156 [TBL] [Abstract][Full Text] [Related]
14. Dystonia during feeding as an early sign of dopa-responsive dystonia. Chieng KS; Hussain N; Gosalakkal JA Pediatr Neurol; 2007 Sep; 37(3):215-7. PubMed ID: 17765812 [TBL] [Abstract][Full Text] [Related]
15. Dopa-responsive dystonia caused by tyrosine hydroxylase deficiency: Three cases report and literature review. Dong HY; Feng JY; Yue XJ; Shan L; Jia FY Medicine (Baltimore); 2020 Aug; 99(33):e21753. PubMed ID: 32872068 [TBL] [Abstract][Full Text] [Related]
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18. [Dopa-responsive dystonia (Segawa syndrome) with secondary skeleton deformity]. Budrewicz SP; Góral M; Koszewicz M; Tarantowicz P; Podemski R Wiad Lek; 2006; 59(9-10):713-5. PubMed ID: 17338136 [TBL] [Abstract][Full Text] [Related]
19. Ataxia telangiectasia like disorder: Another dopa-responsive disorder look-alike? Ser MH; Tekgül Ş; Gündüz A; Kızıltan ME; Kızıltan G; Başak AN Parkinsonism Relat Disord; 2020 May; 74():22-24. PubMed ID: 32289520 [No Abstract] [Full Text] [Related]
20. [Tyrosine hydroxylase deficiency: a case of autosomal recessive dopa-responsive dystonia]. Tan D; Zhang Y; Ye J; Han L; Qiu W; Gu X; Zhang H Zhonghua Er Ke Za Zhi; 2014 Aug; 52(8):616-9. PubMed ID: 25224241 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]