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Prominent Neuroleptic Sensitivity in a Case of Early-onset Alzheimer Disease due to Presenilin-1 G206A Mutation

机译：由于Presenilin-1 G206A突变而引起的早发性阿尔茨海默氏病的突出的抗精神病药敏感性

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摘要

ObjectiveWe describe atypical motor and cognitive features in a case of familial Alzheimer disease (FAD) due to presenilin-1 (PS-1) mutation.

机译：目的我们描述由早老素1（PS-1）突变引起的家族性阿尔茨海默病（FAD）的非典型运动和认知特征。

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期刊名称 other
作者
Steven P. Cercy; Martin J. Sadowski; Thomas Wisniewski;
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年(卷),期 -1(21),3
年度 -1
页码 190–195
总页数 13
原文格式 PDF
正文语种
中图分类
关键词
Alzheimer disease presenilin-1 extrapyramidal signs neuroleptic sensitivity;

机译：阿尔茨海默氏病;早老素-1;锥体束外征兆;抗精神病药敏感性;

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专利

1. Prominent behavioural and psychiatric symptoms in early-onset Alzheimer's disease in a sib pair with the presenilin-1 gene R269G mutation. [J] . Doran M, Larner AJ European archives of psychiatry and clinical neuroscience . 2004,第3期

机译：在早老性早老性阿尔茨海默氏病中，具有早老素-1基因R269G突变的同胞对中出现明显的行为和精神症状。
2. Early-Onset Alzheimer Disease in a Puerto Rican Man with the G206A Mutation in Presenilin 1 (PSEN1) [J] . Bonnin Jose, Garringer Holly, Epperson Francine, Journal of Neuropathology and Experimental Neurology: Official Journal of the American Association of Neuropathologists, Inc . 2018,第6期

机译：在Puerto Rican Man中早期出现的Alzheimer疾病，Pareanilin 1（Psen1）中的G206A突变
3. Genotype-phenotype analysis in early-onset Alzheimer's disease due to presenilin-1 mutations at codon 139. [J] . Hanisch F, Kolmel HW European journal of medical research. . 2004,第7期

机译：由于139位密码子的presenilin-1突变，在早发性阿尔茨海默氏病中进行了基因型-表型分析。
4. Effective Connectivity Changes in Presymptomatie Alzheimer's Disease with E280A Presenilin-1 Mutation Gene [C] . J. Ochoa, F. Sanchez, C. Tobon Latin American Congress on Biomedical Engineering . 2015

机译：Barymptomatie Alzheimer疾病的有效连通性变化e280a presenilin-1突变基因
5. The involvement of hereditary hemochromatosis mutations (C282Y and H63D) in familial Alzheimer disease and Parkinson disease and their purported origins through epidemic pathogenic selection [D] . Moalem, Sharon. 2003

机译：遗传性血细胞化突变（C282Y和H63D）在家族性阿尔茨海默病和帕金森病中的涉及及其通过流行病致病选择所称的起源
6. A presenilin-1 truncating mutation is present in two cases with autopsy-confirmed early-onset Alzheimer disease. [O] . C Tysoe, J Whittaker, J Xuereb, 1998

机译：尸检证实的早发性阿尔茨海默氏病的两个案例中存在presenilin-1截断突变。
7. Prominent Neuroleptic Sensitivity in a Case of Early-onset Alzheimer Disease due to Presenilin-1 G206A Mutation [O] . Steven P. Cercy, Martin J. Sadowski, Thomas Wisniewski 2008

机译：由于PreseniNiN-1 G206A突变，在早熟阿尔茨海默病的情况下显着的神经溶血性敏感性

Prominent Neuroleptic Sensitivity in a Case of Early-onset Alzheimer Disease due to Presenilin-1 G206A Mutation

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