501 related articles for article (PubMed ID: 31800013)
1. Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence.
Morales-Briceño H; Mohammad SS; Post B; Fois AF; Dale RC; Tchan M; Fung VSC
Brain; 2020 Mar; 143(3):751-770. PubMed ID: 31800013
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Autosomal recessive parkinsonism.
Bonifati V
Parkinsonism Relat Disord; 2012 Jan; 18 Suppl 1():S4-6. PubMed ID: 22166450
[TBL] [Abstract][Full Text] [Related]
4. Parkinsonism, movement disorders and genetics in frontotemporal dementia.
Baizabal-Carvallo JF; Jankovic J
Nat Rev Neurol; 2016 Mar; 12(3):175-85. PubMed ID: 26891767
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism.
Yoshino H; Tomiyama H; Tachibana N; Ogaki K; Li Y; Funayama M; Hashimoto T; Takashima S; Hattori N
Neurology; 2010 Oct; 75(15):1356-61. PubMed ID: 20938027
[TBL] [Abstract][Full Text] [Related]
6. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
Brashear A; Dobyns WB; de Carvalho Aguiar P; Borg M; Frijns CJ; Gollamudi S; Green A; Guimaraes J; Haake BC; Klein C; Linazasoro G; Münchau A; Raymond D; Riley D; Saunders-Pullman R; Tijssen MA; Webb D; Zaremba J; Bressman SB; Ozelius LJ
Brain; 2007 Mar; 130(Pt 3):828-35. PubMed ID: 17282997
[TBL] [Abstract][Full Text] [Related]
7. A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing.
Lin CH; Chen PL; Tai CH; Lin HI; Chen CS; Chen ML; Wu RM
Mov Disord; 2019 Apr; 34(4):506-515. PubMed ID: 30788857
[TBL] [Abstract][Full Text] [Related]
8. Novel ATP13A2 (PARK9) homozygous mutation in a family with marked phenotype variability.
Santoro L; Breedveld GJ; Manganelli F; Iodice R; Pisciotta C; Nolano M; Punzo F; Quarantelli M; Pappatà S; Di Fonzo A; Oostra BA; Bonifati V
Neurogenetics; 2011 Feb; 12(1):33-9. PubMed ID: 20853184
[TBL] [Abstract][Full Text] [Related]
9. Rare causes of dystonia parkinsonism.
Schneider SA; Bhatia KP
Curr Neurol Neurosci Rep; 2010 Nov; 10(6):431-9. PubMed ID: 20694531
[TBL] [Abstract][Full Text] [Related]
10. Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.
Magrinelli F; Mehta S; Di Lazzaro G; Latorre A; Edwards MJ; Balint B; Basu P; Kobylecki C; Groppa S; Hegde A; Mulroy E; Estevez-Fraga C; Arora A; Kumar H; Schneider SA; Lewis PA; Jaunmuktane Z; Revesz T; Gandhi S; Wood NW; Hardy JA; Tinazzi M; Lal V; Houlden H; Bhatia KP
Mov Disord; 2022 Jan; 37(1):148-161. PubMed ID: 34622992
[TBL] [Abstract][Full Text] [Related]
11. Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.
Paisán-Ruiz C; Guevara R; Federoff M; Hanagasi H; Sina F; Elahi E; Schneider SA; Schwingenschuh P; Bajaj N; Emre M; Singleton AB; Hardy J; Bhatia KP; Brandner S; Lees AJ; Houlden H
Mov Disord; 2010 Sep; 25(12):1791-800. PubMed ID: 20669327
[TBL] [Abstract][Full Text] [Related]
12. Parkinsonism and dystonia: Clinical spectrum and diagnostic clues.
Morales-Briceno H; Fung VSC; Bhatia KP; Balint B
J Neurol Sci; 2022 Feb; 433():120016. PubMed ID: 34642024
[TBL] [Abstract][Full Text] [Related]
13. Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.
Wu RM; Bounds R; Lincoln S; Hulihan M; Lin CH; Hwu WL; Chen J; Gwinn-Hardy K; Farrer M
Arch Neurol; 2005 Jan; 62(1):82-7. PubMed ID: 15642853
[TBL] [Abstract][Full Text] [Related]
14. Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review.
Chu YT; Lin HY; Chen PL; Lin CH
BMC Neurol; 2020 Mar; 20(1):101. PubMed ID: 32183746
[TBL] [Abstract][Full Text] [Related]
15. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
Sweney MT; Newcomb TM; Swoboda KJ
Pediatr Neurol; 2015 Jan; 52(1):56-64. PubMed ID: 25447930
[TBL] [Abstract][Full Text] [Related]
16. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease.
Di Fonzo A; Chien HF; Socal M; Giraudo S; Tassorelli C; Iliceto G; Fabbrini G; Marconi R; Fincati E; Abbruzzese G; Marini P; Squitieri F; Horstink MW; Montagna P; Libera AD; Stocchi F; Goldwurm S; Ferreira JJ; Meco G; Martignoni E; Lopiano L; Jardim LB; Oostra BA; Barbosa ER; ; Bonifati V
Neurology; 2007 May; 68(19):1557-62. PubMed ID: 17485642
[TBL] [Abstract][Full Text] [Related]
17. Chapter 33: the history of movement disorders.
Lanska DJ
Handb Clin Neurol; 2010; 95():501-46. PubMed ID: 19892136
[TBL] [Abstract][Full Text] [Related]
18. Early-onset autosomal-recessive parkinsonian-pyramidal syndrome.
Lai HJ; Lin CH; Wu RM
Acta Neurol Taiwan; 2012 Sep; 21(3):99-107. PubMed ID: 23196729
[TBL] [Abstract][Full Text] [Related]
19. Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders.
Montaut S; Tranchant C; Drouot N; Rudolf G; Guissart C; Tarabeux J; Stemmelen T; Velt A; Fourrage C; Nitschké P; Gerard B; Mandel JL; Koenig M; Chelly J; Anheim M;
JAMA Neurol; 2018 Oct; 75(10):1234-1245. PubMed ID: 29913018
[TBL] [Abstract][Full Text] [Related]
20. X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.
Di Lazzaro G; Magrinelli F; Estevez-Fraga C; Valente EM; Pisani A; Bhatia KP
Mov Disord; 2021 Jul; 36(7):1511-1525. PubMed ID: 33960519
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
