1. He has raised money for muscular dystrophy charities.

2. In only a few cases, such as muscular dystrophy and cystic fibrosis, has the gene and its protein been identified.

3. Sufian had one client with muscular dystrophy who needed to take every Wednesday off work, so he could rest his muscles.

4. Objective Perform gene diagnosis for Chinese facioscapulohumeral muscular dystrophy(FSHD).

5. What is neuromuscular disease and muscular dystrophy?

5.

6. She was the poster child for muscular dystrophy.

7. Myotonic muscular dystrophy is a rare hereditary disease involved with multiple sys tems. only a few cases were reported in our country.

8. Duchene's muscular dystrophy and cystic fibrosis are examples of hereditary diseases that result from nonsense mutations.

9. Conditions such as muscular dystrophy, spina bifida and tetraplegia will fall under this classification.

10. Background: Duchenne muscular dystrophy is characterized by progressive cardiac dysfunction and myocardial fibrosis late process.

11. Clinical for muscular dystrophy, myasthenia gravis, muscular dystrophy, polymyositis, motor neuron disease, as atrophy disease syringomyelia.

12. In patients with certain types of muscular dystrophy, it is particularly important to be aware of the potential for malignant hyperthermia (MH).

13. Diseases like multiple sclerosis, muscular dystrophy or polio can leave people disabled.

14. The FacioScapuloHumeral Muscular Dystrophy Society addresses issues and needs related to this disease of the skeletal muscle, which is a type of muscular dystrophy.

15. These are genetic disorders that only affect males normally. They are things like muscular dystrophy and haemophilia.

16. In 1847 he described two boys with what was obviously pseudo-hypertrophic muscular dystrophy, described twenty-one years later by Guillaume Duchenne.

17. The researchers hope that their results will allow them to initiate studies in humans with limb-girdle muscular dystrophy.

18. Absence of the carboxy terminus of dystrophin is associated with severe phenotypes in most muscular dystrophy patients.

19. Claims must be made within two years of the child's birth, or four in the case of muscular dystrophy.

20. In the early 1980s, her son Peter died at 15 of muscular dystrophy.

21. Objective To study affected muscle selectivity and main laboratorial examination value of duchenne muscular dystrophy ( DMD ).

22. Some diseases prominent within the European population that could see numbers drop as mixed-race grow are cystic fibrosis, coeliac disease, muscular dystrophy and haemophilia.

23. Swine flu outbreaks have prompted temporary closure of Indiana-based Camp Livingston, a YMCA day camp in West Virginia, and all of the Muscular Dystrophy Association's summer programs.

24. But quantities was larger. Conclusion The capacity of muscle fibers regeneration in pseudohypertrophic muscular dystrophy was correlated with age.

25. Neurasthenia, neurasthenic syndrome, peripheral neuropathy, etc. amyotrophy, myasthenia, progressive muscular dystrophy.

26. Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy(FSHD)in order to improve its diagnosis.

27. Objective To investigate the genealogical tree of women with Becker muscular dystrophy (BMD).

28. Objective To perform early and presymptomatic diagnosis for facioscapulohumeral muscular dystrophy (FSHD).

29. Objective To establish a normative procedure for clinical prenatal gene diagnosis of Duchenne and Becker muscular dystrophy(DMD/BMD).

30. Objective: To investigate the pulmonary function characteristics and rehabilitation strategy for Becker muscular dystrophy(BMD).

31. But it could also make it easier to treat Parkinson's disease, motor neurone disease and muscular dystrophy.

32. Wilson'disease was often misdiagnosed as various kinds of hepatitis, lunacy, falling sickness, arthritis, muscular dystrophy, nephritis, et al, with the misdiagnosis rate of 55.5%.

33. Conclusion Repeat sequence polymorphism as well as gene dosage analysis can potentially be used in carrier detection in the deleted families of Duchenne and Becker muscular dystrophy.

34. Patients with myotonic dystrophy , the most common form of adult-onset muscular dystrophy , have a high prevalence of insulin resistance due to disruption of the insulin receptor.

35. Quick movements cause muscle stiffening. There is also a myotonic form of muscular dystrophy.

36. Objective To develop and compare the methods for determining the carrier status in the 18 deleted families of Duchenne and Becker muscular dystrophy.

37. To explore the application of freeze etching electrom microscopy in the study of Duchenne muscular dystrophy ( DMD ).

38. He had muscular dystrophy.

39. Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy (FSHD) 1A gene.

40. Objective : To observe bone marrow rebuilding after bone marrow transplantation ( BMT ) to treat Duchenne muscular dystrophy ( DMD ).

41. Objective To detect dystrophin gene deletion of Duchenne muscular dystrophy ( DMD ) and make DMD gene diagnosis.