Editorial: Diagnosis of childhood spinal muscular atrophy.
出版信息
Br Med J. 1973 Oct 6;4(5883):2-3. doi: 10.1136/bmj.4.5883.2.
Abstract
摘要
相似文献
1
Editorial: Diagnosis of childhood spinal muscular atrophy.社论：儿童脊髓性肌萎缩症的诊断
Br Med J. 1973 Oct 6;4(5883):2-3. doi: 10.1136/bmj.4.5883.2.
2
Spinal muscular atrophy.
Minn Med. 1971 Jun;54(6):457-61.
3
[Type II proximal spinal muscular atrophy. Clinical, electrophysiological, histopathological and histochemical studies].[II型近端脊髓性肌萎缩症。临床、电生理、组织病理学及组织化学研究]
Minerva Pediatr. 1974 Jun 23;26(22):1125-45.
4
[Clinical study of muscular atrophy].[肌肉萎缩的临床研究]
Hokkaido Igaku Zasshi. 1974 Jan;49(1):23-31.
5
The nosology of the spinal muscular atrophies.脊髓性肌萎缩症的疾病分类学
J Med Genet. 1971 Dec;8(4):481-95. doi: 10.1136/jmg.8.4.481.
6
[Variant of childhood spinal amyotrophy].[儿童脊髓性肌萎缩症的变异型]
Zh Nevropatol Psikhiatr Im S S Korsakova. 1971;71(10):1456-61.
7
[Malate dehydrogenase activity in patients with different forms of progressive muscular dystrophy].[不同类型进行性肌营养不良患者的苹果酸脱氢酶活性]
Zh Nevropatol Psikhiatr Im S S Korsakova. 1970;70(9):1309-12.
8
[Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy].[肌电图对韦尼克-霍夫曼婴儿型脊髓性肌萎缩症诊断的贡献]
Pathol Biol (Paris). 1972 Mar;20(5):287-96.
9
Werdnig-Hoffmann-Wohlfart-Kugelberg-Welander disease. Nosological unity and clinical variability in intrafamilial cases.韦尔尼格－霍夫曼－沃尔夫法特－库格尔贝格－韦兰德病。家族性病例中的疾病分类一致性与临床变异性。
Acta Genet Med Gemellol (Roma). 1971 Jan;20(1):43-58. doi: 10.1017/s1120962300011707.
本文引用的文献
1
INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY.婴儿型肌肉萎缩症。一项前瞻性研究，特别关注一种缓慢进展型。
Brain. 1964 Dec;87:707-18. doi: 10.1093/brain/87.4.707.
2
Infantile muscular atrophy.婴儿型肌肉萎缩症
Arch Neurol. 1961 Aug;5:140-64. doi: 10.1001/archneur.1961.00450140022003.
3
Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.遗传性家族性青少年型肌肉萎缩症，类似肌营养不良症。
AMA Arch Neurol Psychiatry. 1956 May;75(5):500-9. doi: 10.1001/archneurpsyc.1956.02330230050005.
4
Microcephaly and mental subnormalitiy in chronic progressive spinal muscular atrophy of childhood.儿童慢性进行性脊髓性肌萎缩症中的小头畸形和智力发育迟缓
Dev Med Child Neurol. 1967 Oct;9(5):594-601. doi: 10.1111/j.1469-8749.1967.tb02330.x.
5
Benign spinal muscular atrophy arising in childhood and adolescence.
J Neurol Sci. 1967 Jul-Aug;5(1):121-58. doi: 10.1016/0022-510x(67)90013-5.
6
"Myopathic" changes in chronically denervated muscle.慢性失神经支配肌肉中的“肌病性”改变。
Arch Neurol. 1967 Jan;16(1):14-24. doi: 10.1001/archneur.1967.00470190018002.
7
Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease.婴儿期神经源性肌肉萎缩伴生存期延长。韦尔尼克-霍夫曼病的可变病程。
Brain. 1969 Mar;92(1):9-24. doi: 10.1093/brain/92.1.9.
8
The benign proximal spinal progressive muscular atrophies.良性近端脊髓性进行性肌萎缩症
Acta Neurol Scand. 1968;44(5):542-60. doi: 10.1111/j.1600-0404.1968.tb05591.x.
9
10
Spinal muscular atrophy in childhood. Two clues to clinical diagnosis.儿童脊髓性肌萎缩症。临床诊断的两条线索。
Arch Dis Child. 1973 May;48(5):386-8. doi: 10.1136/adc.48.5.386.
Zotero 插件