Progranulin Mutations are a Common Cause of FTLD in Northern Italy

被引：21

作者：

Benussi, Luisa ^{[1
]}

Ghidoni, Roberta ^{[1
,2
]}

Binetti, Giuliano ^{[1
]}

机构：

[1] IRCCS Ctr S Giovanni di Dio FBF, NeuroBioGen Lab Memory Clin, Brescia, Italy

[2] IRCCS Ctr S Giovanni di Dio FBF, Prote Unit, Brescia, Italy

来源：

ALZHEIMER DISEASE & ASSOCIATED DISORDERS | 2010年 / 24卷 / 03期

关键词：

FRONTOTEMPORAL LOBAR DEGENERATION; CBS;

D O I：

10.1097/WAD.0b013e3181d1bb13

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：308 / 309

页数：3

共 7 条

[1] A novel deletion in progranulin gene is associated with FTDP-17 and CBS [J].

Benussi, Luisa ;

Binetti, Giuliano ;

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Ghidoni, Roberta .

NEUROBIOLOGY OF AGING, 2008, 29 (03) :427-435

[2] Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide [J].

Benussi, Luisa ;

Ghidoni, Roberta ;

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[3] PGRN Mutations in Northern Italy [J].

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[4] Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members [J].

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[5] Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration [J].

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[6] Granulin Mutations Associated With Frontotemporal Lobar Degeneration and Related Disorders: An Update [J].

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HUMAN MUTATION, 2008, 29 (12) :1373-1386

[7] Higher Than Expected Progranulin Mutation Rate in a Case Series of Italian FTLD Patients [J].

Tremolizzo, Lucio ;

Gelosa, Giorgio ;

Galbussera, Alessio ;

Isella, Valeria ;

Arosio, Cristina ;

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ALZHEIMER DISEASE & ASSOCIATED DISORDERS, 2009, 23 (03) :301-301

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