269 results on '"Yan, Xin-Xiang"'
Search Results
2. Association of rare PPARGC1A variants with Parkinson’s disease risk
3. PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment
4. Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
5. Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease
6. Coding mutations in NUS1 contribute to Parkinson’s disease
7. GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study
8. The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients
9. A neurophysiological profile in Parkinson’s disease with mild cognitive impairment and dementia in China
10. The single nucleotide polymorphism Rs12817488 is associated with Parkinson’s disease in the Chinese population
11. Analysis of GIPC1 CGG repeat expansions in essential tremor
12. The contribution of GIGYF2 to Parkinson’s disease: a meta-analysis
13. Evaluating the role of ARSA in Chinese patients with Parkinson's disease
14. Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal Study
15. The Association Between Lysosomal Storage Disorder Genes and Parkinson’s Disease: A Large Cohort Study in Chinese Mainland Population
16. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic
17. UQCRC1 variants in Parkinson’s disease: a large cohort study in Chinese mainland population
18. Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism
19. LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population
20. Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism
21. Association of the DRD2 and DRD3 polymorphisms with response to pramipexole in Parkinson’s disease patients
22. Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han
23. Polygenic determinants of Parkinson's disease in a Chinese population
24. PSAP variants in Parkinson’s disease: a large cohort study in Chinese mainland population
25. Additional file 5 of GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study
26. Additional file 1 of GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study
27. Additional file 2 of GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study
28. Additional file 3 of GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study
29. Low-frequency and rare coding variants of NUS1 contribute to pathogenesis and phenotype of Parkinson’s disease: a case-control study
30. Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor
31. A new variant of the ATP13A2 gene in Chinese patients with early-onset parkinsonism
32. Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings
33. Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism
34. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders
35. Impaired iPLA2β activity affects iron uptake and storage without iron accumulation: An in vitro study excluding decreased iPLA2β activity as the cause of iron deposition in PLAN
36. Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's Disease
37. Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor.
38. Alzheimer’s disease susceptibility genes modify the risk of Parkinson disease and Parkinson’s disease-associated cognitive impairment
39. Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene
40. Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene
41. Identification of Ser465 as a novel PINK1 autophosphorylation site
42. Identifying the presence of Parkinson’s disease using low-frequency fluctuations in BOLD signals
43. RAB39B gene mutations are not linked to familial Parkinson’s disease in China
44. Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia
45. Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population
46. Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based study
47. Exon dosage analysis of parkin gene in Chinese sporadic Parkinson’s disease
48. VPS35 gene variants are not associated with Parkinson's disease in the mainland Chinese population
49. Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism
50. Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.