| 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. | 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。 |
| 6. | 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。 |
| 7. | A gene implicated in spinal muscular atrophy showed an association in three populations , but not in yoruba from ibadan , nigeria
一个涉及脊髓性肌萎缩病的基因显示出与三个人群有关联但却没有在伊巴丹、尼日利亚、的优鲁巴人身上发现。 |
| 8. | Methods : we used deidentified , family - reported data from participants in the international spinal muscular atrophy patient registry and obtained additional clinical information through a mail - in questionnaire
方法：应用来源于国际脊肌萎缩症患者注册处的鉴定、家庭报道数据，并通过邮寄问卷的形式获得更多的临床信息。 |
| 9. | Background : noninvasive ventilation has become increasingly available to spinal muscular atrophy ( sma ) patients since the early 1990s . this is expected to have improved survival for sma type 1 patients
背景：自90年代早期，非侵入性通气越来越广泛的应用于脊肌萎缩症（ sma ）患者，被认为提高了1型脊肌萎缩症患者的生存率。 |
