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2. Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease

7. OTHER NMDs

12. Wernicke encephalopathy and Creutzfeldt-Jakob disease

13. Mechanisms underlying Andersen's syndrome pathology in skeletal muscle are revealed in human myotubes

15. Long-term benefit of enzyme replacement therapy with alglucosidase alfa in adults with Pompe disease: prospective analysis from the French Pompe Registry

16. Lethal paradoxical cerebral vein thrombosis due to suspicious anticoagulant rodenticide intoxication with chlorophacinone

20. Épendymomes intracrâniens de l'adulte. Diagnostic histologique et facteurs histopronostiques

22. Imagerie du nerf facial

26. Scientific correspondence

29. Self-report questionnaire vs. clinical evaluation form in the French National Registry on facioscapulohumeral dystrophy: a statistical comparison

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

34. Abstracts

41. Current French Pompe Prevalence Study (French PoPS)

46. Diffusion-weighted imaging in normal fetal brain maturation

48. Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families

49. Long-term exposure to Myozyme results in a decrease of anti-drug antibodies in late-onset Pompe disease patients

50. Effect of enzyme replacement therapy with alglucosidase alfa (Myozyme®) in 12 patients with advanced late-onset Pompe disease

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