The LRRK2 G2019S Mutation Predisposes Parkinson's Disease Patients to Cancer

被引:0
|
作者
Inzelberg, Rivka
Cohen, Oren S.
Aharon-Peretz, Judith
Schlesinger, Ilana
Yaakov, Zichron
Gershoni-Baruch, Ruth
Djaldetti, Ruth
Nitzan, Zeev
Ephraty, Lilach
Tunkel, Olga
Kozlova, Evgenya
Inzelberg, Lilah
Schechtman, Edna
Kaplan, Natali
Friedman, Eitan
Hassin-Baer, Sharon
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
下载
收藏
页码:A17 / A17
页数:1
相关论文
共 50 条
  • [41] LRRK2 G2019S mutation does not contribute to Parkinson's disease in South India
    Vijayan, Bejoy
    Gopala, Srinivas
    Kishore, Asha
    NEUROLOGY INDIA, 2011, 59 (02) : 157 - 160
  • [42] The G2019S LRRK2 mutation is frequent in north African families with Parkinson's disease
    Lesage, S.
    Ibanez, P.
    Lohmann, E.
    Pollak, P.
    Tison, F.
    Tazir, M.
    Leutenegger, A. L.
    Guimaraes, J.
    Bonnet, A. M.
    Durr, A.
    Brice, A.
    EUROPEAN JOURNAL OF NEUROLOGY, 2005, 12 : 31 - 32
  • [43] A meta-analysis of the prevalence of the mutation LRRK2 G2019S in patients with Parkinson's disease in Africa
    Wahmane, Sofiane Ait
    Achbani, Abderrahmane
    Elatiqi, Mohamed
    Belmouden, Ahmed
    Nejmeddine, Mohamed
    GENE REPORTS, 2021, 24
  • [44] The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: Clinical and demographic characteristics
    Mabel Gatto, Emilia
    Parisi, Virginia
    Paola Converso, Daniela
    Jose Poderoso, Juan
    Cecilia Carreras, Maria
    Felix Marti-Masso, Jose
    Paisan-Ruiz, Coro
    NEUROSCIENCE LETTERS, 2013, 537 : 1 - 5
  • [45] LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson's disease patients
    Bardien, Soraya
    Marsberg, Angelica
    Keyser, Rowena
    Lombard, Debbie
    Lesage, Suzanne
    Brice, Alexis
    Carr, Jonathan
    JOURNAL OF NEURAL TRANSMISSION, 2010, 117 (07) : 847 - 853
  • [46] The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease -: Is there a gender effect?
    Orr-Urtreger, A.
    Shifrin, C.
    Rozovski, U.
    Rosner, S.
    Bercovich, D.
    Gurevich, T.
    Yagev-More, H.
    Bar-Shira, A.
    Giladi, N.
    NEUROLOGY, 2007, 69 (16) : 1595 - 1602
  • [47] LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson’s disease patients
    Soraya Bardien
    Angelica Marsberg
    Rowena Keyser
    Debbie Lombard
    Suzanne Lesage
    Alexis Brice
    Jonathan Carr
    Journal of Neural Transmission, 2010, 117 : 847 - 853
  • [48] The G2019S LRRK2 Mutation is Rare in Korean Patients with Parkinson's Disease and Multiple System Atrophy
    Cho, Jin-Whan
    Kim, Sung-Yeon
    Park, Sung-Sup
    Jeon, Beom S.
    JOURNAL OF CLINICAL NEUROLOGY, 2009, 5 (01): : 29 - 32
  • [49] LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease
    Infante, J
    Rodríguez, E
    Combarros, O
    Mateo, I
    Fontalba, A
    Pascual, J
    Oterino, A
    Polo, JM
    Leno, C
    Berciano, J
    NEUROSCIENCE LETTERS, 2006, 395 (03) : 224 - 226
  • [50] Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson's disease
    Chien, Hsin Fen
    Figueiredo, Tamires Rocha
    Hollaender, Marianna Almeida
    Tofoli, Fabiano
    Takada, Leonel Tadao
    Pereira, Lygia do Veiga
    Barbosa, Egberto Reis
    ARQUIVOS DE NEURO-PSIQUIATRIA, 2014, 72 (05) : 356 - 359