260 results on '"Saunders-Pullman, R"'
Search Results
2. Generalized Torsion Dystonia☆
3. DYT13, Cranio-Cervical-Brachial ☆
4. Fahn–Marsden Rating Scale ☆
5. Transcranial sonography and functional imaging in glucocerebrosidase mutation Parkinson disease
6. Compound heterozygous PNPLA6 mutations cause Boucher–Neuhäuser syndrome with late-onset ataxia
7. Epidemiology of laryngeal dystonia (LD): 1441
8. Olfactory discrimination in GNAL mutation dystonia: 1412
9. DYT2, Autosomal Recessive Generalized Dystonia
10. DYT12, Rapid Onset Dystonia-parkinsonism
11. DYT6, Mixed Phenotype Primary Dystonia
12. DYT1
13. DYT4, Autosomal Dominant Type Dystonia or Whispering Dysphonia
14. DYT11, DYT15, Myoclonus-dystonia
15. Dystonia in Amish-Mennonite and Mennonite Families
16. Fahn–Marsden Rating Scale
17. DYT7, Autosomal Dominant Focal Dystonia
18. DYT13, Cranio-Cervical-Brachial
19. Generalized Primary Torsion Dystonia
20. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
21. Gaucher Disease Ascertained through a Parkinson’s Center: Imaging and Clinical Characterization
22. Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes
23. Phenotypic features of myoclonus-dystonia in three kindreds
24. Variant ataxia-telangiectasia presenting as primary-appearing dystonia in Canadian Mennonites.
25. Olfactory dysfunction in LRRK2 G2019S mutation carriers.
26. The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease
27. Metabolic changes in DYT11 myoclonus-dystonia
28. Age at onset as a factor in determining the phenotype of primary torsion dystonia.
29. Gender differences in the IL6 −174G>C and ESR2 1730G>A polymorphisms and the risk of Parkinson's disease
30. Gender differences in the risk of familial parkinsonism: Beyond LRRK2?
31. Etiology of musician's dystonia: Familial or environmental?
32. Metabolomic profiling to develop blood biomarkers for Parkinson's disease
33. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers
34. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene
35. Dominantly transmitted focal dystonia in families of patients with musician's cramp
36. Sensory abnormalities in unaffected relatives in familial adult-onset dystonia
37. A new screening tool for cervical dystonia
38. High mutation rate in dopa-responsive dystonia: Detection with comprehensiveGCHIscreening
39. The effect of estrogen replacement on early Parkinson's disease.
40. Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test
41. Increased risk for recurrent major depression in DYT1 dystonia mutation carriers
42. Diagnostic criteria for dystonia in DYT1 families
43. Myoclonus dystonia
44. Idiopathic torsion dystonia linked to chromosome 8 in two mennonite families
45. Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.
46. Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence.
47. Olfactory dysfunction in LRRK2G2019S mutation carriers
48. Age at onset as a factor in determining the phenotype of primary torsion dystonia
49. Sensory abnormalities in unaffected relatives in familial adult-onset dystonia.
50. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCEmutation carriers
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