Epidemiology of Motor-Neuron Diseases

作者: A. Roger Bobowick , Jacob A. Brody

DOI: 10.1056/NEJM197305172882005

关键词: Progressive muscular atrophyAmyotrophic lateral sclerosisDiseaseMotor neuronPathologyProgressive bulbar palsyEpidemiologyMedicineGeneral Medicine

摘要: THE motor-neuron diseases as considered here include the clinical syndromes that have been shown to be due primary abnormalities of anterior-horn cells and motor cranial-nerve nuclei. The term disease is used in a more restricted sense for syndrome amyotrophic lateral sclerosis components, progressive muscular atrophy bulbar palsy. Although these disorders similar pathologic substrate expression, they do not necessarily share same causal factors. Some are clearly hereditary, sporadic 95 per cent cases. In recent years, distinctions between major . . .

参考文章(84)
A. Vejjajiva, J.B. Foster, H. Miller, Motor neuron disease Journal of the Neurological Sciences. ,vol. 4, pp. 299- 314 ,(1967) , 10.1016/0022-510X(67)90108-6
K. Kondo, T. Tsubaki, F. Sakamoto, The ryukyuan muscular atrophy Journal of the Neurological Sciences. ,vol. 11, pp. 359- 382 ,(1970) , 10.1016/0022-510X(70)90082-1
A.J Mccomas, R.E.P Sica, M.J Campbell, "Sick" motoneurones. A unifying concept of muscle disease. The Lancet. ,vol. 297, pp. 321- 325 ,(1971) , 10.1016/S0140-6736(71)91045-2
B.O. Osuntokun, The pattern of neurological illness in tropical Africa Journal of the Neurological Sciences. ,vol. 12, pp. 417- 442 ,(1971) , 10.1016/0022-510X(71)90110-9
SYLVIA HAY, INCIDENCE OF SELECTED CONGENITAL MALFORMATIONS IN IOWA American Journal of Epidemiology. ,vol. 94, pp. 572- 584 ,(1971) , 10.1093/OXFORDJOURNALS.AJE.A121356
E. KUGELBERG, Heredofamilial Juvenile muscular Atrophy Simulating muscular Dystrophy Archives of Neurology And Psychiatry. ,vol. 75, pp. 500- 509 ,(1956) , 10.1001/ARCHNEURPSYC.1956.02330230050005
Kurt Boman, Tuula Meurman, Prognosis of amyotrophic lateral sclerosis. Acta Neurologica Scandinavica. ,vol. 43, pp. 489- 498 ,(1967) , 10.1111/J.1600-0404.1967.TB05755.X