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1. The Compact Linear Collider (CLIC) - 2018 Summary Report

3. Updated baseline for a staged Compact Linear Collider

7. Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort

8. Diagnostic issues faced by a rare disease healthcare network during Covid-19 outbreak: data from the Campania Rare Disease Registry

11. Using global team science to identify genetic parkinson's disease worldwide

14. Correction to: Monoallelic KIF1A-related disorders: a multicenter cross sectional study and systematic literature review (Journal of Neurology, (2021), 10.1007/s00415-021-10792-3)

15. Utility of the Parkinson's disease-Cognitive Rating Scale for the screening of global cognitive status in Huntington's disease (vol 267, pg 1527, 2020)

16. Ngs in hereditary ataxia: When rare becomes frequent

17. POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients

18. Neuroacanthocytosis Syndromes in an Italian Cohort: Clinical Spectrum, High Genetic Variability and Muscle Involvement

26. GBA-Related Parkinson’s Disease:Dissection of Genotype–Phenotype Correlates in a LargeItalian Cohort

28. The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families

36. CERN Yellow Reports: Monographs, Vol 2 (2018): The Compact Linear e+e− Collider (CLIC) : 2018 Summary Report

42. Fast and accurate SNVs and CNVs screening in Parkinson's Disease Patients using Next-Generation approach

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

48. Using global team science to identify genetic Parkinson's disease worldwide

49. PERK-Mediated Unfolded Protein Response Activation and Oxidative Stress in PARK20 Fibroblasts

50. Using global team science to identify genetic parkinson's disease worldwide

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