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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.

机译：早发性阿尔茨海默病中的app，psEN1和psEN2突变：家族性和散发性病例的遗传筛查研究。

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Hélène-Marie Lanoiselée; Gaël Nicolas; David Wallon; Anne Rovelet-Lecrux; Morgane Lacour; Stéphane Rousseau; Anne-Claire Richard; Florence Pasquier; Adeline Rollin-Sillaire; Olivier Martinaud; Muriel Quillard-Muraine; Vincent de la Sayette; Claire Boutoleau-Bretonniere; Frédérique Etcharry-Bouyx; Valérie Chauviré; Marie Sarazin; Isabelle le Ber; Stéphane Epelbaum; Thérèse Jonveaux; Olivier Rouaud; Mathieu Ceccaldi; Olivier Félician; Olivier Godefroy; Maite Formaglio; Bernard Croisile; Sophie Auriacombe; Ludivine Chamard; Jean-Louis Vincent; Mathilde Sauvée; Cecilia Marelli-Tosi; Audrey Gabelle; Canan Ozsancak; Jérémie Pariente; Claire Paquet; Didier Hannequin; Dominique Campion;
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1. APP , PSEN1 , AND PSEN2 MUTATIONS IN EARLY-ONSET ALZHEIMER’S DISEASE DISCOVERED IN ASIAN COUNTRIES: A GENETIC SCREENING STUDY OF FAMILIAL AND SPORADIC CASES [J] . Giau Van Vo, Gaik-Siew Ch’ng, Vorapun - Senanarong, Alzheimer’s & dementia: the journal of the Alzheimer’s Association . 2018,第7期

机译：在亚洲国家发现的早期Alzheimer疾病中的应用，psen1和psen2突变：家族和散发病例的遗传筛查研究
2. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases [J] . Hélène-Marie Lanoiselée, Ga?l Nicolas, David Wallon, PLoS Medicine . 2017,第3期

机译：早发性阿尔茨海默病的APP，PSEN1和PSEN2突变：家族和散发病例的基因筛选研究
3. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases [J] . Hélène-Marie Lanoiselée, Ga?l Nicolas, David Wallon, PLoS Medicine . 2017,第3期

机译：早发性阿尔茨海默病的APP，PSEN1和PSEN2突变：家族和散发病例的基因筛选研究
4. Ultrastructral Analysis of Synapse in a Drosophila of the Swedish Mutation Which Causes Early-Onset Alzheimer's Disease Using Focused Ion Beam Microscopy [C] . Se Jin Park, Andreas Schertel, Sung Sik Han International Metallographic Society Annual meeting;Microscopy Society of America Annual Meeting;Microanalysis Society Annual meeting . 2011

机译：使用聚焦离子束显微镜在瑞典突变的果蝇中引起早发阿尔茨海默氏病的突触的超微结构分析
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. APP PSEN1 and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases [O] . Hélène-Marie Lanoiselée, Gaël Nicolas, David Wallon, 2017

机译：早发性阿尔茨海默病的APPPSEN1和PSEN2突变：家族和散发病例的基因筛选研究
7. De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. [O] . Dumanchin, C, Brice, A, Campion, D, 1998

机译：从头早老素1突变在临床上偶发，早发的阿尔茨海默氏病病例中很少见。法国阿尔茨海默氏病研究小组。

APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.

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