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2. Prognostic significance and outcomes of patient-reported symptoms after valve intervention in severe aortic stenosis

3. Syncope at rest in severe aortic stenosis may persist after intervention and is associated with poor outcomes

11. Hereditary motor neuropathies

12. Validación de la versión española de la Charcot-Marie-Tooth Disease Pediatric Scale (CMTPedS)

15. Clinical characteristics and outcomes of thymoma associated myasthenia gravis

16. A study of the phenotypic variability and disease progression in Laing myopathy through the evaluation of muscle imaging

17. Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations

18. Clinical, genetic and disability profile of pediatric distal hereditary motor neuropathy

22. CMT caused by MORC2 mutations in Spain

23. Oxidative Stress, a Crossroad between Rare Diseases and Neurodegeneration

24. The relationship between deficit in digit span and genotype in nonsense mutation Duchenne muscular dystrophy

29. 3 Impact of morbid obesity and obesity phenotype on outcomes post transcatheter aortic valve replacement

31. Clinical spectrum of BICD2 mutations

32. PRO93 DEMOGRAPHICS AND TREATMENT PATTERNS FOR CHARCOT-MARIE-TOOTH DISEASE IN THE EU AND US: INTERIM RESULTS FROM AN INTERNATIONAL DIGITAL REAL-WORLD STUDY

33. PRO138 PRODUCTIVITY LOSSES IN PEOPLE WITH CHARCOT-MARIE-TOOTH DISEASE IN THE EU AND US: INTERIM RESULTS FROM AN INTERNATIONAL DIGITAL REAL-WORLD EVIDENCE STUDY

34. PRO37 HEALTHCARE RESOURCE USE IN CHARCOT-MARIE-TOOTH DISEASE IN THE EU AND US: INTERIM RESULTS FROM AN INTERNATIONAL DIGITAL REAL-WORLD STUDY

37. IqYmune® is an effective maintenance treatment for multifocal motor neuropathy: a randomised, double-blind, multicenter cross-over non-inferiority study versus Kiovig® - The LIME Study

38. Characterization of molecular mechanisms underlying the axonal Charcot-Marie-Tooth neuropathy caused by MORC2 mutations

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

44. The width of the third ventricle associates with cognition and behaviour in motor neuron disease

46. Characterising the phenotype and mode of inheritance of patients with inherited peripheral neuropathies carrying MME mutations

47. Infections of the Central Nervous System after Untelated Donor Umbilical Cord Blood Transplantation or Human teukocyte Antigen-Matched Sibling Transplantation

48. Generation of a disease-specific iPS cell line derived from a patient with Charcot-Marie-Tooth type 2K lacking functional GDAP1 gene

49. Audiological Findings in Charcot-Marie-Tooth Disease Type 4C

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