330 related articles for article (PubMed ID: 33154736)
1. A Han Chinese Family With Early-Onset Parkinson's Disease Carrying Novel Frameshift Mutation and Compound Heterozygous Mutation of
Gao C; Huang T; Chen R; Yuan Z; Tian Y; Zhang Y
Front Neurol; 2020; 11():582323. PubMed ID: 33154736
[TBL] [Abstract][Full Text] [Related]
2. Whole exome sequencing identified a new compound heterozygous PRKN mutation in a Chinese family with early-onset Parkinson's disease.
Li T; Kou D; Cui Y; Le W
Biosci Rep; 2020 May; 40(5):. PubMed ID: 32391545
[TBL] [Abstract][Full Text] [Related]
3. Rare and novel variants of PRKN and PINK1 genes in Vietnamese patients with early-onset Parkinson's disease.
Ton ND; Thuan ND; Thuong MTH; Ngoc TTB; Nhung VP; Hoa NTT; Nam NH; Dung HT; Son ND; Ba NV; Bac ND; Tai TN; Dung LTK; Hung NT; Duong NT; Ha NH; Hai NV
Mol Genet Genomic Med; 2020 Oct; 8(10):e1463. PubMed ID: 32856414
[TBL] [Abstract][Full Text] [Related]
4. The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.
Chen YP; Yu SH; Zhang GH; Hou YB; Gu XJ; Ou RW; Shen Y; Song W; Chen XP; Zhao B; Cao B; Zhang LY; Sun MM; Liu FF; Wei QQ; Liu KC; Lin JY; Yang TM; Yang J; Wu Y; Jiang Z; Liu J; Cheng YF; Xiao Y; Su WM; Feng F; Cai YY; Li SR; Hu T; Yuan XQ; Zhou QQ; Shao N; Ma S; Shang HF
Eur J Neurol; 2022 Nov; 29(11):3218-3228. PubMed ID: 35861376
[TBL] [Abstract][Full Text] [Related]
5. Genetic Analysis of Patients With Early-Onset Parkinson's Disease in Eastern China.
Hua P; Zhao Y; Zeng Q; Li L; Ren J; Guo J; Tang B; Liu W
Front Aging Neurosci; 2022; 14():849462. PubMed ID: 35645773
[TBL] [Abstract][Full Text] [Related]
6. Case report: Early-onset Parkinson's disease with initial spastic paraparesis and hyperreflexia caused by compound heterozygous
Jensen I; Hendrich C; Klietz M; Berding G; Höglinger GU; Wegner F
Front Neurol; 2022; 13():969232. PubMed ID: 36468052
[TBL] [Abstract][Full Text] [Related]
7. Genetic Study of Early Onset Parkinson's Disease in Cyprus.
Abu Manneh R; Chairta PP; Mitsi E; Loizidou MA; Georgiou AN; Christou YP; Pantzaris M; Zamba-Papanicolaou E; Hadjisavvas A
Int J Mol Sci; 2022 Dec; 23(23):. PubMed ID: 36499697
[TBL] [Abstract][Full Text] [Related]
8. Dopaminergic Dysfunction and Glucose Metabolism Characteristics in Parkin-Induced Early-Onset Parkinson's Disease Compared to Genetically Undetermined Early-Onset Parkinson's Disease.
Liu FT; Lu JY; Sun YM; Li L; Yang YJ; Zhao J; Ge JJ; Wu P; Jiang JH; Wu JJ; Zuo CT; Wang J
Phenomics; 2023 Feb; 3(1):22-33. PubMed ID: 36939793
[TBL] [Abstract][Full Text] [Related]
9. Novel Compound Heterozygous
Fan K; Hu P; Song C; Deng X; Wen J; Liu Y; Deng H
Parkinsons Dis; 2019; 2019():9024894. PubMed ID: 31929871
[TBL] [Abstract][Full Text] [Related]
10. Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
Zhu W; Huang X; Yoon E; Bandres-Ciga S; Blauwendraat C; Billingsley KJ; Cade JH; Wu BP; Williams VH; Schindler AB; Brooks J; Gibbs JR; Hernandez DG; Ehrlich D; Singleton AB; Narendra DP
Brain; 2022 Jun; 145(6):2077-2091. PubMed ID: 35640906
[TBL] [Abstract][Full Text] [Related]
11. Heterogeneous phenotype in a family with compound heterozygous parkin gene mutations.
Deng H; Le WD; Hunter CB; Ondo WG; Guo Y; Xie WJ; Jankovic J
Arch Neurol; 2006 Feb; 63(2):273-7. PubMed ID: 16476817
[TBL] [Abstract][Full Text] [Related]
12. Expanding the canvas of PRKN mutations in familial and early-onset Parkinson disease.
Pandey S; Tomar LR; Kumar S; Dinesh S; Thelma BK
Parkinsonism Relat Disord; 2019 Sep; 66():216-219. PubMed ID: 31409571
[TBL] [Abstract][Full Text] [Related]
13. Whole-Exome Sequencing Study of Consanguineous Parkinson's Disease Families and Related Phenotypes: Report of Twelve Novel Variants.
Soudyab M; Shariati M; Esfehani RJ; Shalaei N; Vafadar S; Nouri V; Zech M; Winkelmann J; Shoeibi A; Sadr-Nabavi A
J Mol Neurosci; 2022 Dec; 72(12):2486-2496. PubMed ID: 36520381
[TBL] [Abstract][Full Text] [Related]
14. Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease.
Yu E; Rudakou U; Krohn L; Mufti K; Ruskey JA; Asayesh F; Estiar MA; Spiegelman D; Surface M; Fahn S; Waters CH; Greenbaum L; Espay AJ; Dauvilliers Y; Dupré N; Rouleau GA; Hassin-Baer S; Fon EA; Alcalay RN; Gan-Or Z
Mov Disord; 2021 Jan; 36(1):178-187. PubMed ID: 32970363
[TBL] [Abstract][Full Text] [Related]
15. Co-occurrence of PRKN and SYNJ1 variants in Early-Onset Parkinson's disease.
Cotrin JC; Piergiorge RM; Gonçalves AP; Pereira JS; Gerber AL; de Campos Guimarães AP; de Vasconcelos ATR; Santos-Rebouças CB
Metab Brain Dis; 2024 Jun; ():. PubMed ID: 38836947
[TBL] [Abstract][Full Text] [Related]
16. Mutation analysis of the PARKIN, PINK1, DJ1, and SNCA genes in Turkish early-onset Parkinson's patients and genotype-phenotype correlations.
Erer S; Egeli U; Zarifoglu M; Tezcan G; Cecener G; Tunca B; Ak S; Demirdogen E; Kenangil G; Kaleagası H; Dogu O; Saka E; Elibol B
Clin Neurol Neurosurg; 2016 Sep; 148():147-53. PubMed ID: 27455133
[TBL] [Abstract][Full Text] [Related]
17. Genetic study of a Chinese pedigree with early onset Parkinson's disease caused by novel compound heterozygous mutations in
Zhang L; Luo AD; Pan CY; Liu M; Liao SS
Ibrain; 2021 Jun; 7(2):108-112. PubMed ID: 37786907
[TBL] [Abstract][Full Text] [Related]
18. Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K; Funayama M; Billingsley KJ; Malik L; Miano-Burkhardt A; Leonard HL; Makarious MB; Iwaki H; Ding J; Gibbs JR; Ishiguro M; Yoshino H; Ogaki K; Oyama G; Nishioka K; Nonaka R; Akamatsu W; Blauwendraat C; Hattori N
Mov Disord; 2023 Dec; 38(12):2249-2257. PubMed ID: 37926948
[TBL] [Abstract][Full Text] [Related]
19. PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.
Lu CS; Lai SC; Wu RM; Weng YH; Huang CL; Chen RS; Chang HC; Wu-Chou YH; Yeh TH
Am J Med Genet B Neuropsychiatr Genet; 2012 Mar; 159B(2):183-91. PubMed ID: 22213678
[TBL] [Abstract][Full Text] [Related]
20. Genetic analysis of ATP13A2, PLA2G6 and FBXO7 in a cohort of Chinese patients with early-onset Parkinson's disease.
Shen T; Pu J; Lai HY; Xu L; Si X; Yan Y; Jiang Y; Zhang B
Sci Rep; 2018 Sep; 8(1):14028. PubMed ID: 30232368
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
