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78 results on '"Oosterloo M"'

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1. SHAMPOO: A stochastic model for tracking dust particles under the influence of non-local disk processes

2. The role of planetary interior in the long-term evolution of atmospheric CO2 on Earth-like exoplanets

6. Reader Response: Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease

8. De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability

11. Clinical and genetic characteristics of late-onset Huntington's disease

12. The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature

13. Infections in deep brain stimulation: Shaving versus not shaving

15. Deep Brain Stimulation of the internal globus pallidus in refractory Tourette Syndrome

18. Severe course of Lyme neuroborreliosis in an HIV-1 positive patient; case report and review of the literature

19. Diagnostic image (283). A man with a swollen tongue

21. Possible confusion between primary hypersomnia and adult attention-deficit/hyperactivity disorder.

22. Severe course of Lyme neuroborreliosis in an HIV-1 positive patient; case report and review of the literature

23. Fear of choking and fear of falling in middle and end stage patients with Huntington’s disease

24. Preferences for genetic interventions for SCA and Huntington's disease: results of a discrete choice experiment among patients.

25. Navigating Life With Parkinson's Disease: A Focus Group Study on Coping Strategies and Considerations for Self-Management Support.

26. A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder.

27. High Levels of Mutant Huntingtin Protein in Tear Fluid From Huntington's Disease Gene Expansion Carriers.

28. Genetic Interventions for Spinocerebellar Ataxia and Huntington's Disease: A Qualitative Study of the Patient Perspective.

29. Facilitators and barriers in caring for a person with Huntington's disease: input for a remote support program.

30. Clinical Review of Juvenile Huntington's Disease.

32. Psychotropic medication use in Huntington's disease: A retrospective cohort study.

33. The cross-sectional area of the vagus nerve is not reduced in Parkinson's disease patients.

34. Teaching Video NeuroImage: Improvement in Motor Development After Start of Levodopa in Tyrosine Hydroxylase Deficiency.

35. Disease Onset in Huntington's Disease: When Is the Conversion?

36. Predictive genetic testing in Huntington's disease: should a neurologist be involved?

37. De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability.

38. Diagnosing Juvenile Huntington's Disease: An Explorative Study among Caregivers of Affected Children.

39. Measuring the quality of care in nursing home residents with early-onset neurodegenerative diseases: a scoping review.

40. The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature.

42. Clinical and genetic characteristics of late-onset Huntington's disease.

43. Obsessive-Compulsive and Perseverative Behaviors in Huntington's Disease.

44. Infections in deep brain stimulation: Shaving versus not shaving.

46. A detailed analysis of intracerebral hemorrhages in DBS surgeries.

47. Is There Convincing Evidence that Intermediate Repeats in the HTT Gene Cause Huntington's Disease?

49. A new mutation for Huntington disease following maternal transmission of an intermediate allele.

50. An experimental model for Huntington's chorea?

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