49 results on '"van de Warrenburg, Bart P"'
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2. The patchy tremor landscape: recent advances in pathophysiology
3. Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia
4. Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force
5. A single session of cerebellar theta burst stimulation does not alter writing performance in writer’s cramp
6. De novo gain-of-function and loss-of-function mutations of SCN8A in patients with intellectual disabilities and epilepsy
7. Reliability and Validity of the Range of Motion Scale (ROMS) in Patients with Abnormal Postures
8. Serum angiogenin levels are elevated in ALS, but not Parkinsonʼs disease
9. Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6
10. Cognitive Impairment in “Other” Movement Disorders: Hidden Defects and Valuable Clues
11. Early onset dystonia and parkinsonism with abnormal globus pallidal signal in MRI: A diagnostic challenge
12. Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet
13. Is TOR1A a risk factor in adult-onset primary torsion dystonia?
14. Autosomal Recessive Spinocerebellar Ataxia 7 (SCAR7) is Caused by Variants in TPP1, The Gene Involved in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis 2 Disease (CLN2 Disease)
15. Phenotypic Variability in a Dystonia Family With Mutations in the Manganese Transporter Gene
16. Promotion of physical activity and fitness in sedentary patients with Parkinson’s disease: randomised controlled trial
17. Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6
18. Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism
19. Mutations in potassium channel kcnd3 cause spinocerebellar ataxia type 19
20. Phenotypes and genetic architecture of focal primary torsion dystonia
21. Genotype–phenotype correlations in spastic paraplegia type 7: a study in a large Dutch cohort
22. Republished: A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into order
23. Association of BDNF Met66Met polymorphism with arm tremor in cervical dystonia
24. Angiogenin, a Piece of the Complex Puzzle of Neurodegeneration
25. Re-emergent Tremor in a Dystonic SWEDD Case†‡
26. Presence of ATM Protein and Residual Kinase Activity Correlates with the Phenotype in Ataxia-Telangiectasia: A Genotype–Phenotype Study†
27. Cerebellar theta burst stimulation impairs eyeblink classical conditioning
28. Cerebellar theta burst stimulation impairs eyeblink classical conditioning
29. Angiogenin Variants in Parkinson Disease and Amyotrophic Lateral Sclerosis
30. How might physical activity benefit patients with Parkinson disease?
31. Patients with primary cervical dystonia have evidence of discrete deficits in praxis
32. Movement disorders in spinocerebellar ataxias†
33. Cerebellar brain inhibition is decreased in active and surround muscles at the onset of voluntary movement
34. DYT6 dystonia: Mutation screening, phenotype, and response to deep brain stimulation
35. Pallidopyramidal disease: A misnomer?
36. The clinical approach to movement disorders
37. There might be more to SPG4!
38. Repetitive transcranial magnetic stimulation for levodopa-induced dyskinesias in Parkinsonʼs disease
39. Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6
40. Cortical excitability is abnormal in patients with the “fixed dystonia” syndrome
41. REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31
42. The syndrome of (predominantly cervical) dystonia and cerebellar ataxia: new cases indicate a distinct but heterogeneous entity
43. PRKCG mutation (SCA-14) causing a Ramsay Hunt phenotype
44. Pisa syndrome after unilateral pallidotomy in Parkinson’s disease: an unrecognised, delayed adverse event?
45. Postural responses to multidirectional stance perturbations in cerebellar ataxia
46. Recent Advances in Hereditary Spinocerebellar Ataxias
47. Spinocerebellar Ataxia and Peripheral Neuropathy
48. Peripheral Nerve Involvement in Spinocerebellar Ataxias
49. SCA19 and SCA22: evidence for one locus with a worldwide distribution
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