共 1078 条
[91]
Perry EK(2011)Translation initiator EIF4G1 mutations in familial Parkinson disease Am J Hum Genet. 89 398-e1e95
[92]
Tiraboschi P(2002)Familial diffuse Lewy body disease, eye movement abnormalities, and distribution of pathology Arch Neurol. 59 464-175
[93]
Attems J(2002)Clinical presentations in monozygotic twins with dementia with Lewy bodies J Am Med Dir Assoc. 3 175-1276
[94]
Thomas A(2016)Exome sequencing in dementia with Lewy bodies Transl Psychiatry. 6 e728-735
[95]
Brown A(2014)Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodies Hum Mol Genet. 23 6139-1661
[96]
Jaros E(2018)Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study Lancet neurology. 17 64-630
[97]
Lett DJ(2018)The Genetics of Dementia with Lewy Bodies: Current Understanding and Future Directions Curr Neurol Neurosci Rep. 18 67-203
[98]
Montine TJ(2017)An update on the genetics of dementia with Lewy bodies Parkinsonism Relat Disord. 43 1-4902
[99]
Phelps CH(2006)Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype Arch Neurol. 63 370-24
[100]
Beach TG(2013)APOE epsilon4 increases risk for dementia in pure synucleinopathies JAMA Neurol. 70 223-6473