Search

Your search keyword '"Meco, G."' showing total 550 results

Search Constraints

Start Over You searched for: Author "Meco, G." Remove constraint Author: "Meco, G."
550 results on '"Meco, G."'

Search Results

5. Genetic Complexity and Parkinson's Disease

6. Depressive symptoms in Parkinson’s disease and in non-neurological medical illnesses

7. A Wide Database for a Multicenter Study on Pneumocystis jirovecii Pneumonia in Intensive Care Units

10. Clinical characteristics of long-term survivors in multiple system atrophy: An analysis of the EMSA-SG registry: 299

11. Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

12. The European Multiple System Atrophy-Study Group (EMSA-SG)

18. The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson’s disease and originates from a common ancestor

20. Motor and non-motor outcomes in patients with advanced Parkinson's disease treated with levodopa/carbidopa intestinal gel: final results of the GREENFIELD observational study

22. Epidemiology of multiple system atrophy

23. Epidemiology of progressive supranuclear palsy

29. Which patients discontinue? Issues on Levodopa/carbidopa intestinal gel treatment: Italian multicentre survey of 905 patients with long-term follow-up

33. PRKAR1B mutation associated with a new neurodegenerative disorder with unique pathology

37. The PRIAMO study: age- and sex-related relationship between prodromal constipation and disease phenotype in early Parkinson's disease.

39. Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes

40. PARK6 is a common cause of familial parkinsonism

43. The parkin gene and its phenotype

46. Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study

47. The PRIAMO study: A multicenter assessment of nonmotor symptoms and their impact on quality of life in Parkinson's disease

49. Frontal assessment battery scores and non-motor symptoms in parkinsonian disorders

50. GIGYF2 mutations are not a frequent cause of familial Parkinson's disease

Catalog

Books, media, physical & digital resources