user

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：
来源：
NEUROLOGY | 2011年 / 76卷 / 09期
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：A17 / A17
页数：1
相关论文
共 50 条
  • [1] The LRRK2 G2019S mutation predisposes Parkinson's disease patients to cancer
    Inzelberg, R.
    Cohen, O.
    Aharon-Peretz, J.
    Schlesinger, I.
    Gershoni-Baruch, R.
    Djaldetti, R.
    Nitsan, Z.
    Ephraty, L.
    Tunkel, O.
    Kozlova, E.
    Inzelberg, L.
    Kaplan, N.
    Schechtman, E.
    Friedman, E.
    Hassin-Baer, S.
    MOVEMENT DISORDERS, 2011, 26 : S310 - S310
  • [2] The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease
    Cho, J.
    Kim, H.
    Park, S.
    Jeon, B.
    MOVEMENT DISORDERS, 2006, 21 : S402 - S402
  • [3] LRRK2 G2019S Mutation in an Argentinean Cohort of Patients with Parkinson's Disease
    Gatto, Emilia M.
    Converso, Daniela P.
    Marti-Masso, Jose F.
    Sebastian, San
    Ruiz, Coro Paisan
    Persi, Gabriel
    Etcheverry, Jose L.
    Parisi, Virginia
    Leiguarda, Fernando
    Carreras, Maria C.
    Poderoso, Juan J.
    NEUROLOGY, 2010, 74 (09) : A253 - A253
  • [4] The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease
    Cho, Jin-Whan
    Kim, Sung-Yeon
    Park, Sung-Sup
    Kim, Han-Jun
    Ahn, Tae-Beom
    Kim, Jong-Min
    Jeon, Beom-Seok
    CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 2007, 34 (01) : 53 - 55
  • [5] Mitochondrial impairment in patients with Parkinson disease with the G2019S mutation in LRRK2
    Mortiboys, Heather
    Johansen, Krisztina K.
    Aasly, Jan O.
    Bandmann, Oliver
    NEUROLOGY, 2010, 75 (22) : 2017 - 2020
  • [6] Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease
    Lesage, Suzanne
    Leclere, Laurence
    Lohmann, Ebba
    Borg, Michel
    Ruberg, Merle
    Duerr, Alexandra
    Brice, Alexis
    NEURODEGENERATIVE DISEASES, 2007, 4 (2-3) : 195 - 198
  • [7] Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's disease
    Tiziana Squillaro
    Franca Cambi
    Giuseppe Ciacci
    Simone Rossi
    Monica Ulivelli
    Alessandro Malandrini
    Maria Antonietta Mencarelli
    Francesca Mari
    Alessandra Renieri
    Francesca Ariani
    Journal of Human Genetics, 2007, 52 : 201 - 204
  • [8] Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation
    Deng, H
    Le, WD
    Guo, Y
    Hunter, CB
    Xie, WJ
    Jankovic, J
    ANNALS OF NEUROLOGY, 2005, 57 (06) : 933 - 934
  • [9] Frequency of the LRRK2 G2019S mutation in South African patients with Parkinson's disease
    du Toit, Nicola
    van Coller, Riaan
    Anderson, David G.
    Carr, Jonathan
    Bardien, Soraya
    NEUROGENETICS, 2019, 20 (04) : 215 - 218
  • [10] Frequency of the LRRK2 G2019S mutation in Italian patients affected by Parkinson's disease
    Squillaro, Tiziana
    Cambi, Franca
    Ciacci, Giuseppe
    Rossi, Simone
    Ulivelli, Monica
    Malandrini, Alessandro
    Mencarelli, Maria Antonietta
    Mari, Francesca
    Renieri, Alessandra
    Ariani, Francesca
    JOURNAL OF HUMAN GENETICS, 2007, 52 (03) : 201 - 204
12345