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2. Sex contribution to average age at onset of Huntington’s disease depends on the number of (CAG)n repeats.

3. Safety and efficacy of pridopidine in patients with Huntington's disease (PRIDE-HD): a phase 2, randomised, placebo-controlled, multicentre, dose-ranging study

5. Saccades in Huntington's Disease.

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

16. Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study

18. Cognitive decline in Huntington's disease expansion gene carriers

19. Safety and efficacy of pridopidine in patients with Huntington's disease (PRIDE-HD): a phase 2, randomised, placebo-controlled, multicentre, dose-ranging study

20. A study in a Polish ataxia cohort indicates genetic heterogeneity and points to MTCL1 as a novel candidate gene

24. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

25. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

35. Depresja psychotyczna jako początkowy objaw choroby Huntingtona - opis przypadku.

38. Huntington Quality of Life Instrument

39. Identification of genetic variants associated with Huntington's disease progression

40. Clinical manifestations of intermediate allele carriers in Huntington disease

41. The contribution of gender differences in motor, behavioral and cognitive features to functional capacity, independence and quality of life in patients with Huntington's disease

43. Huntington' disease--imbalance of amino acid levels in plasma of patients and mutation carriers.

44. [Vertebral arteries dissection as a rare cause of central nervous system ischemia].

45. Association of influenza incidence with multiple sclerosis onset.

46. [Clinical picture of patients with Huntington's disease in relation to the number of trinucleotide CAG repeats in IT-15 gene].

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