Mutations in LRRK2 - A clinical and genetic study in a Portuguese population

被引:0
|
作者
Morgadinho, AS
Bras, JM
Januario, C
Cunha, L
Hardy, J
Oliveira, C
机构
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
引用
收藏
页码:S57 / S57
页数:1
相关论文
共 50 条
  • [21] Clinical Expression of LRRK2 G2019S Mutations in the Elderly
    San Luciano, Marta
    Lipton, Richard B.
    Wang, Cuiling
    Katz, Mindy
    Zimmerman, Molly E.
    Sanders, Amy E.
    Ozelius, Laurie J.
    Bressman, Susan B.
    Saunders-Pullman, Rachel
    MOVEMENT DISORDERS, 2010, 25 (15) : 2571 - 2576
  • [22] Clinical features of LRRK2 parkinsonism
    Haugarvoll, Kristoffer
    Wszolek, Zbigniew K.
    PARKINSONISM & RELATED DISORDERS, 2009, 15 : S205 - S208
  • [23] Neuron-autonomous susceptibility to induced synuclein aggregation is exacerbated by endogenous Lrrk2 mutations and ameliorated by Lrrk2 genetic knock-out
    MacIsaac, Sarah
    Melo, Thaiany Quevedo
    Zhang, Yuting
    Volta, Mattia
    Farrer, Matthew J.
    Milnerwood, Austen J.
    BRAIN COMMUNICATIONS, 2020, 2 (01)
  • [24] LRRK2 and GBA genetic mutations are not uncommon in an unselected Ashkenazi elderly cohort with PD
    Isaacson, S.
    Isaacson, J.
    MOVEMENT DISORDERS, 2018, 33 : S616 - S616
  • [25] Genetic analysis of LRRK2 in Parkinson's disease in Han Chinese population
    Zhang, Jin-Ru
    Jin, Hong
    Li, Kai
    Mao, Cheng-Jie
    Yang, Ya-Ping
    Wang, Fen
    Gu, Chen-Chen
    Zhang, Hui-Jun
    Chen, Jing
    Liu, Chun-Feng
    NEUROBIOLOGY OF AGING, 2018, 72 : 187.e5 - 187.e10
  • [26] LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population
    Cilia, Roberto
    Siri, Chiara
    Rusconi, Damiana
    Allegra, Roberta
    Ghiglietti, Andrea
    Sacilotto, Giorgio
    Zini, Michela
    Zecchinelli, Anna L.
    Asselta, Rosanna
    Duga, Stefano
    Paganoni, Anna M.
    Pezzoli, Gianni
    Seia, Manuela
    Goldwurm, Stefano
    PARKINSONISM & RELATED DISORDERS, 2014, 20 (08) : 911 - 914
  • [27] Screening for LRRK2 mutations in patients with Parkinson's disease in Russia:: identification of a novel LRRK2 variant
    Pchelina, S. N.
    Yakimovskii, A. F.
    Emelyanov, A. K.
    Ivanova, O. N.
    Schwarzman, A. L.
    Singleton, A. B.
    EUROPEAN JOURNAL OF NEUROLOGY, 2008, 15 (07) : 692 - 696
  • [28] LRRK2 Exon 41 mutations are not common in Turkey
    Hanagasi, H. A.
    Lohmann, E.
    Dursun, B.
    Honore, A.
    Lesage, S.
    Aydin, O.
    Babacan, G.
    Gurvit, H.
    Yazici, J.
    Erginel-Unaltuna, N.
    Brice, A.
    Emre, M.
    MOVEMENT DISORDERS, 2009, 24 : S141 - S141
  • [29] LRRK2 mutations in autosomal-dominant parkinsonism
    Gasser, T
    MOVEMENT DISORDERS, 2006, 21 : S3 - S4
  • [30] The Evolution of Genetic Variability at the LRRK2 Locus
    Guenther, Dylan T.
    Follett, Jordan
    Amouri, Rim
    Ben Sassi, Samia
    Hentati, Faycel
    Farrer, Matthew J.
    GENES, 2024, 15 (07)