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

5. Actinomycose de la paroi abdominale

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

9. Vaginal birth in a patient with Pompe disease

14. Improving outcome measures in late onset Pompe disease: Modified Rasch-Built Pompe-Specific Activity scale.

15. Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry.

16. Real-life effectiveness 1 year after switching to avalglucosidase alfa in late-onset Pompe disease patients worsening on alglucosidase alfa therapy: A French cohort study.

17. Characteristics of Patients With Late-Onset Pompe Disease in France: Insights From the French Pompe Registry in 2022.

18. Macroglossia: A potentially severe complication of late-onset Pompe disease.

19. Motor and respiratory decline in patients with late onset Pompe disease after cessation of enzyme replacement therapy during COVID-19 pandemic.

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

21. Large variation in effects during 10 years of enzyme therapy in adults with Pompe disease.

22. Late-onset Pompe disease in France: molecular features and epidemiology from a nationwide study.

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

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

25. Multidisciplinary care allowing uneventful vaginal delivery in a woman with Pompe disease.

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