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

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

5. Treatment with docosahexaenoic acid in Spinocerebellar Ataxia 38

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

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

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

10. Genetic counselling in ALS: facts, uncertainties and clinical suggestions

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

12. CHCH10 mutations in an Italian cohort of familial and sporadic amyotrophic lateral sclerosis patients

13. Prediction of late/early arrivals in container terminals – A qualitative approach

14. Nuove strategie gestionali per la competitività di un terminal container di transhipment: sviluppo di strumenti di supporto alle decisioni per la pianificazione delle attività portuali

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

17. Development of prediction models for container traffic

19. TBK1 is associated with ALS and ALS-FTD in Sardinian patients

20. ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

26. Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomized, double blind, placebo controlled, phase III study

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

28. Prediction of arrival times and human resources allocation for container terminal

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

30. ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry

31. Il papiro conciliare P.Vindob. G 3: un 'originale' sulla via da Costantinopoli a Ravenna (e a Vienna)

32. Liquid Biopsy, the hype vs. hope in molecular and clinical oncology.

33. Long-term efficacy of docosahexaenoic acid (DHA) for Spinocerebellar Ataxia 38 (SCA38) treatment: An open label extension study.

34. Docosahexaenoic acid is a beneficial replacement treatment for spinocerebellar ataxia 38.

35. Respiratory sleep disorders in Jeune syndrome: a case description.

36. The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonisms.

37. Compressive behaviour of child and adult cortical bone.

38. [Retroperitoneal sarcomas: our experience].

39. [Papillary microcarcinoma of the thyroid. Clinical implications and therapeutic strategy].

40. [Therapeutic strategies in differentiated cancer of the thyroid: total thyroidectomy].

41. [Neonatal choledocholithiasis: a case report].

42. [Ovarian cysts in the differential diagnosis of acute and recurrent abdominal pains].

43. Juvenile Huntington's disease.

44. [Relevance and therapeutic implications of dysplasia in the follow-up of ulcerative rectocolitis].

45. [Idiopathic focal glomerulosclerosis in West syndrome. Observation of a case].

47. [Diagnostic problems of primary malignant gastric lymphomas].

48. [Atrial flutter in a newborn infant. Recent case].

49. [The Kawasaki syndrome. Report of a case].

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