Characterization of the Neuropsychiatric Features Associated with Mutations in C9ORF72'MAPT and PGRN

被引：0
|
作者：
Adeli, Anahita [1 ]
Geda, Yonas [1 ]
Boeve, Bradley [1 ]
Graff-Radford, Neill [2 ]
DeJesus-Hernandez, Mariely [2 ]
Knopman, David [1 ]
Josephs, Keith [1 ]
Pedraza, Otto [2 ]
Rush, Beth [2 ]
Fields, Julie [1 ]
Rutherford, Nicola [2 ]
Baker, Matthew [2 ]
Smith, Glenn [1 ]
Ivnik, Robert [1 ]
Pankratz, Vernon [1 ]
Rademakers, Rosa [2 ]
Petersen, Ronald [1 ]
机构：
[1] Mayo Clin, Rochester, MN USA
[2] Mayo Clin, Jacksonville, FL 32224 USA
来源：
NEUROLOGY | 2012年 / 78卷
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P05065
引用
收藏
页数：3
相关论文
共 50 条
  • [41] Treatment implications of C9ORF72
    Sha, Sharon J.
    Boxer, Adam
    ALZHEIMERS RESEARCH & THERAPY, 2012, 4 (06)
  • [42] Treatment implications of C9ORF72
    Sharon J Sha
    Adam Boxer
    Alzheimer's Research & Therapy, 4
  • [43] Investigating mechanism of C9orf72 mutations in amyotrophic lateral sclerosis
    Kim, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 320 - 320
  • [44] C9orf72 and intracerebral hemorrhage
    Hostettler, Isabel C.
    Bernal-Quiros, Manuel
    Wong, Andrew
    Sharma, Nikhil
    Wilson, Duncan
    Seiffge, David J.
    Shakeshaft, Clare
    Jaeger, Hans R.
    Cohen, Hannah
    Yousry, Tarek
    Salman, Rustam Al-Shahi
    Lip, Gregory Y. H.
    Brown, Martin M.
    Muir, Keith W.
    Werring, David J.
    Houlden, Henry
    NEUROBIOLOGY OF AGING, 2019, 84 : 237.e1 - 237.e3
  • [45] The clinical and pathological phenotypes of frontotemporal dementia with C9ORF72 mutations
    Liu, Ying
    Yu, Jin-Tai
    Sun, Fu-Rong
    Ou, Jiang-Rong
    Qu, Song-Ben
    Tan, Lan
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2013, 335 (1-2) : 26 - 35
  • [46] Microglia in frontotemporal lobar degeneration with progranulin or C9ORF72 mutations
    Sakae, Nobutaka
    Roemer, Shanu F.
    Bieniek, Kevin F.
    Murray, Melissa E.
    Baker, Matthew C.
    Kasanuki, Koji
    Graff-Radford, Neill R.
    Petrucelli, Leonard
    Van Blitterswijk, Marka
    Rademakers, Rosa
    Dickson, Dennis W.
    ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2019, 6 (09): : 1782 - 1796
  • [47] CORTICAL HYPEREXCITABILITY IN PATIENTS WITH C9ORF72 MUTATIONS: RELATIONSHIP TO PHENOTYPE
    Schanz, Olivia
    Bageac, Devin
    Braun, Laura
    Traynor, Bryan J.
    Lehky, Tanya J.
    Floeter, Mary Kay
    MUSCLE & NERVE, 2016, 54 (02) : 264 - 269
  • [48] Development of an AAV gene therapy for C9orf72 ALS by targeting mutant C9orf72 transcripts
    Zancanella, Vanessa
    de Ruiter, Anna Aster
    van Vliet, Romy
    van Rooijen, Kristel
    Chatterjee, Madhurima
    Pereira, Ines
    Shtefaniuk, Vlad
    Kieper, Sebastian
    Bockaj, Irena
    de Miguel, Elena
    Dobrynin, Greg
    Evers, Melvin
    Valls, Mercedes
    Kovacevic, Jovana
    Liu, Ying Poi
    MUSCLE & NERVE, 2023, 68 : S70 - S70
  • [49] A case of Neuromyotonia associated to a C9ORF72 CCCGG expansion
    Bonapace, G.
    Gullace, R.
    Procopio, R.
    Gaglardi, M.
    Fortunato, F.
    Gambardella, A.
    Valentino, P.
    Annesi, G.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2020, 28 (SUPPL 1) : 433 - 434
  • [50] Parkinson disease is not associated with C9ORF72 repeat expansions
    Harms, Matthew B.
    Neumann, Drexel
    Benitez, Bruno A.
    Cooper, Breanna
    Carrell, David
    Racette, Brad A.
    Perlmutter, Joel S.
    Goate, Alison
    Cruchaga, Carlos
    NEUROBIOLOGY OF AGING, 2013, 34 (05) : 1519.e1 - 1519.e2
12345