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Volumn 24, Issue 4, 2009, Pages 618-619

Parkinsonism and impulse control disorder: Presentation of a new progranulin gene mutation

Author keywords

[No Author keywords available]

Indexed keywords

LEVODOPA; PROGRANULIN; GRN PROTEIN, HUMAN; SIGNAL PEPTIDE;

EID: 67651151267     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22429     Document Type: Letter
Times cited : (9)

References (10)
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    • Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive includsion with progranulin gene mutations
    • Josephs KA, Ahmed Z, Katsus O, et al. Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive includsion with progranulin gene mutations. J Neuropathol Exp Neurol 2007;66:142-151.
    • (2007) J Neuropathol Exp Neurol , vol.66 , pp. 142-151
    • Josephs, K.A.1    Ahmed, Z.2    Katsus, O.3
  • 2
    • 39749135522 scopus 로고    scopus 로고
    • Phenotype variability in progranulin mutation carriers: A clinical, neuropsychological imaging, and genetic study
    • Le Ber I, Camuzat A, Hannequin D, et al. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological imaging, and genetic study. Brain 2008;131:732-746.
    • (2008) Brain , vol.131 , pp. 732-746
    • Le Ber, I.1    Camuzat, A.2    Hannequin, D.3
  • 5
    • 0032543684 scopus 로고    scopus 로고
    • Association of missense and 5′-splice-site mutation in tau with inherited dementia FTDP-17
    • Hutton M, Lendon CL, Rizzu P, et al. Association of missense and 5′-splice-site mutation in tau with inherited dementia FTDP-17. Nature 1998;393:702-705.
    • (1998) Nature , vol.393 , pp. 702-705
    • Hutton, M.1    Lendon, C.L.2    Rizzu, P.3
  • 6
    • 33746919083 scopus 로고    scopus 로고
    • Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
    • Baker M, Mackenzie IR, Pickering-Brown SM, et al. Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 2006;442:916-919.
    • (2006) Nature , vol.442 , pp. 916-919
    • Baker, M.1    Mackenzie, I.R.2    Pickering-Brown, S.M.3
  • 7
    • 33746910649 scopus 로고    scopus 로고
    • Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
    • Cruts M, Gijselinck I, van der Zee J, et al. Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 2006;442:920-924
    • (2006) Nature , vol.442 , pp. 920-924
    • Cruts, M.1    Gijselinck, I.2    van der Zee, J.3
  • 8
    • 33750590113 scopus 로고    scopus 로고
    • The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene
    • Mackenzie IRA, Baker M, Pickering-Brown S, et al. The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene. Brain 2006;129:3081-3090.
    • (2006) Brain , vol.129 , pp. 3081-3090
    • Mackenzie, I.R.A.1    Baker, M.2    Pickering-Brown, S.3
  • 9
    • 33749568019 scopus 로고    scopus 로고
    • Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
    • Gass J, Cannon A, Mackenzie IR, et al. Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration. Hum Mol Genet 2006;15:2988-3001.
    • (2006) Hum Mol Genet , vol.15 , pp. 2988-3001
    • Gass, J.1    Cannon, A.2    Mackenzie, I.R.3
  • 10
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    • A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
    • Beck J, Rohrer JD, Campbell T, et al. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series. Brain 2008;131: 706-720.
    • (2008) Brain , vol.131 , pp. 706-720
    • Beck, J.1    Rohrer, J.D.2    Campbell, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.