相似文献
1
[Current conceptions on etiology, pathogenesis and treatment of motor neuron disease].
Zh Nevrol Psikhiatr Im S S Korsakova. 2005;105(1):4-12.
2
[Motor neuron disease].
Tanpakushitsu Kakusan Koso. 2004 May;49(7 Suppl):1127-8.
3
Genetics of sporadic amyotrophic lateral sclerosis.
Hum Mol Genet. 2007 Oct 15;16 Spec No. 2:R233-42. doi: 10.1093/hmg/ddm215.
4
Axonal defects in mouse models of motoneuron disease.
J Neurobiol. 2004 Feb 5;58(2):272-86. doi: 10.1002/neu.10313.
5
Facial onset sensory motor neuronopathy (FOSMN) syndrome: an unusual amyotrophic lateral sclerosis phenotype?
J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):951. doi: 10.1136/jnnp-2014-307756. Epub 2014 Mar 18.
6
Analysis of the survival motor neuron and neuronal apoptosis inhibitory protein genes in Malay patients with Spinal Muscular Atrophy.
Med J Malaysia. 2004 Oct;59(4):512-4.
7
Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients.
Clin Neurol Neurosurg. 2007 Dec;109(10):844-8. doi: 10.1016/j.clineuro.2007.07.019. Epub 2007 Sep 11.
8
SMN1 gene, but not SMN2, is a risk factor for sporadic ALS.
Neurology. 2006 Oct 10;67(7):1147-50. doi: 10.1212/01.wnl.0000233830.85206.1e. Epub 2006 Aug 23.
9
[Molecular mechanisms of motor neuron disease].
Zh Nevrol Psikhiatr Im S S Korsakova. 2005;105(4):68-76.
10
[A study of survival motor neuron and neuronal apoptosis inhibitory protein gene in spinal muscular atrophy].
Zhonghua Nei Ke Za Zhi. 2001 Jun;40(6):401-4.
Zotero 插件