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Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutationDOI 10.1001/jama.277.10.793
Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation.Semantic proximity
Phenotypic profile of early-onset familial Alzheimer's disease caused by presenilin-1 E280A mutation.Semantic proximity
Presenilin-1 mutations in Alzheimer's disease: an update on genotype-phenotype relationships.Semantic proximity
Atypical presentation of a novel Presenilin 1 R377W mutation: sporadic, late-onset Alzheimer disease with epilepsy and frontotemporal atrophy.Semantic proximity
Presenilin-1 mutations in Alzheimer's disease.Semantic proximity
Early- and Late-Onset Alzheimer’s Disease: Two Sides of the Same Coin?Semantic proximity
The solved and unsolved mysteries of the genetics of early-onset Alzheimer's disease.Semantic proximity
Early-Onset Alzheimer's Disease: What Is Missing in Research?Semantic proximity
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.Semantic proximity
Early-onset familial Alzheimer's disease (EOFAD).Semantic proximity
Clinical phenotype of G206D mutation in the presenilin 1 gene in pathologically confirmed familial Alzheimer's disease.Semantic proximity
Early psychiatrics symptoms in familial Alzheimer's disease with presenilin 1 mutation (I83T).Semantic proximity
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