399 results on '"Bressman, Susan B"'
Search Results
2. Multiple sclerosis in LRRK2 G2019S Parkinson's disease and isolated nigral degeneration in a homozygous variant carrier.
3. Treatment of Generalized Dystonia
4. Digitized Spiral Drawing: A Possible Biomarker for Early Parkinson's Disease.
5. REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers
6. Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?
7. Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish‐Mennonites
8. Cognitive and Motor Function in Long-Duration PARKIN-Associated Parkinson Disease
9. Mutations in GNAL cause primary torsion dystonia
10. Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism
11. Disordered network structure and function in dystonia: pathological connectivity vs. adaptive responses
12. Differences in Sex‐Specific Frequency of Glucocerebrosidase Variant Carriers and Familial Parkinsonism
13. Disordered network structure and function in dystonia: Pathological connectivity vs. adaptive responses
14. Clinical profiles and outcomes of deep brain stimulation in G2019S LRRK2 Parkinson disease
15. Movement Disorders
16. Progression in the LRRK2-Asssociated Parkinson Disease Population
17. Disruption of network for visual perception of natural motion in primary dystonia
18. Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2 G2019S Variant
19. Movement Disorders
20. Assessment of Glucocerebrosidase Enzyme Activity in Parkinson Disease Using Multiple Approaches
21. Diagnosis and Management of Dystonia
22. The visual perception of natural motion: abnormal task-related neural activity in DYT1 dystonia
23. Low-variance RNAs identify Parkinsonʼs disease molecular signature in blood
24. Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study
25. Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression
26. Research priorities in spasmodic dysphonia
27. Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes
28. Reply: Dystonia After Severe Head Injuries
29. What’s new in dystonia?
30. Cognitive Functioning of Glucocerebrosidase (GBA) Non-manifesting Carriers
31. Genetics of dystonia: an overview
32. A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia
33. Early-Onset Hand Tremor and Later Adult Progression Without Speech Involvement: An Unusual DYT6 Presentation
34. Phenomenology and classification of dystonia: A consensus update
35. Primary dystonia: Moribund or viable
36. Rapid-onset dystonia-parkinsonism
37. Association of Olfactory Performance With Motor Decline and Age at Onset in People With Parkinson Disease and the LRRK2G2019S Variant
38. Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism
39. The diagnosis of dystonia
40. Dystonia
41. Pallidal deep brain stimulation for DYT6 dystonia
42. Lrrk2 G2019s Mutations May Be Increased in Puerto Ricans
43. Milestones in Dystonia
44. Phenotypic Spectrum of Musicianʼs Dystonia: A Task-Specific Disorder?
45. Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation
46. DYT1, An Inherited Dystonia
47. Contributor's List
48. Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia
49. Frequency of Known Mutations in Early-Onset Parkinson Disease: Implication for Genetic Counseling: The Consortium on Risk for Early Onset Parkinson Disease Study
50. LRRK2 and GBA Variants Exert Distinct Influences on Parkinson’s Disease-Specific Metabolic Networks
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