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5. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

6. Superhydrophobic lab-on-chip measures secretome protonation state and provides a personalized risk assessment of sporadic tumour

7. Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis

8. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

9. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

10. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636, 2021)

11. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (Nature Genetics, (2021), 53, 12, (1636-1648), 10.1038/s41588-021-00973-1)

14. Effect modification of the association between total cigarette smoking and ALS risk by intensity, duration and time-since-quitting: Euro-MOTOR

15. Theme 10 - Disease Stratification and Phenotyping of Patients.

16. Theme 02 - Genetics and Genomics.

17. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

18. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

19. Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

22. Multicentre, cross-cultural, population-based, case-control study of physical activity as risk factor for amyotrophic lateral sclerosis

23. Association between alcohol exposure and the risk of amyotrophic lateral sclerosis in the Euro-MOTOR study

29. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

32. Late mortality and causes of death among 5-year survivors of childhood cancer diagnosed in the period 1960–1999 and registered in the Italian Off-Therapy Registry

33. Human Fibrinogen Concentrate and Fresh Frozen Plasma in the Management of Severe Acquired Hypofibrinogenemia in Children with Acute Lymphoblastic Leukemia: Results of a Retrospective Survey

34. Late mortality and causes of death among 5-year survivors of childhood cancer diagnosed in the period 1960–1999 and registered in the Italian Off-Therapy Registry

35. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis

37. Effetti e meccanismi molecolari della Curcumina nelle leucemie linfoblasti che acute dell’età pediatrica

38. Enhancer Role of rMnSOD in apoptosis triggering by daunorubicin of pediatric B-ALL cells

42. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

43. Reduced-Intensity delayed intensification in standard-Risk pediatric acute lymphoblastic leukemia defined by undetectable minimal residual disease: Results of an international randomized trial (AIEOP-BFM ALL 2000)

44. Reduced-Intensity delayed intensification in standard-Risk pediatric acute lymphoblastic leukemia defined by undetectable minimal residual disease: Results of an international randomized trial (AIEOP-BFM ALL 2000)

45. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

46. HFE p.H63D polymorphism does not influence ALS phenotype and survival

47. Sistemi foraggeri dinamici a servizio della biodiversità

48. Rischio di recidiva nel linfoma di Hodgkin pediatrico: dalla esperienza AIEOP ad una strategia europea

49. A case-control study of hormonal exposures as etiologic factors for ALS in women

50. ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion

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