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1. A standardised protocol for blood and cerebrospinal fluid collection and processing for biomarker research in ataxia.

3. Characterization of Lifestyle in Spinocerebellar Ataxia Type 3 and Association with Disease Severity

15. Suicidal ideation in a European Huntington's disease population

20. The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

21. Entrepreneurship education literature in the 2000s

22. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

23. Cruzamento de patologias na síndrome de Tourette: uma revisão sistemática

27. A importância do jogo simbólico no desenvolvimento da criança de dois anos

30. Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

31. Mitochondrial function in Parkinson's disease cybrids containing an nt2 neuron-like nuclear background

32. Association of HFE common mutations with Parkinson's disease, Alzheimer's disease and mild cognitive impairment in a Portuguese cohort

33. Independent patterns of damage within magno-, parvo- and koniocellular pathways in Parkinson's disease

35. Results of a multicenter SPECT study with [123I]-Iodolisuride in extrapyramidal syndromes

37. Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus.

42. Trinucleotide Repeats in 202 Families With Ataxia[sub n] Allele at the SCA17 Locus.

50. Gut-first Parkinson's disease is encoded by gut dysbiome.

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