| 1. | Familial progressive spinal muscular atrophy
家族性进行性脊肌萎缩 |
| 2. | Progressive spinal muscular atrophy
进行性脊髓性肌萎缩 |
| 3. | Prenatal diagnosis of spinal muscular atrophy based on umbilical cord blood
胎儿脐带血产前诊断脊髓性肌萎缩症 |
| 4. | Chronic spinal muscular atrophy
慢性脊髓性肌萎缩 |
| 5. | Biological and histological changes of denervated skeletal muscular atrophy
失神经支配骨骼肌萎缩的生物学和组织学变化 |
| 6. | Clinical observation on treatment of 56 cases of muscular atrophy by combined jiaji and body acupuncture
夹脊刺结合体针治疗肌萎缩56例临床观察 |
| 7. | Some patients experience only minor symptoms , while others may develop spinal muscular atrophy
一些患者只会出现轻微徵状，但也有患者会出现脊骨肌肉萎缩的情况。 |
| 8. | The purposes of physical therapy are to , improve facial circulation , and if possible , delay muscular atrophy following nerve degeneration , and to re - educate patient
物理治疗的方式包括红内线、冰敷、电刺激、按摩及脸部运动等。 |
| 9. | Conclusion : survival in spinal muscular atrophy type 1 patients has increased in recent years , in relation to the growing trend toward more proactive clinical care
结论：近年来1型脊肌萎缩症幸存者增加归功于主动临床护理的增长。 |
| 10. | There is loss of anterior horn cells , so that patients present with progressive weakness that proceeds to paralysis from neurogenic muscular atrophy
存在前角细胞丧失,因此病人表现为渐进性衰弱，这可能因神经源性肌萎缩而出现瘫痪。 |
