메뉴 건너뛰기




Volumn 71, Issue 1, 2014, Pages 62-67

Cognitive and motor function in long-duration PARKIN-associated parkinson disease

(36)  Alcalay, Roy N a   Caccappolo, Elise a   Mejia Santana, Helen a   Tang, Ming Xin a   Rosado, Llency a   Reilly, Martha Orbe a   Ruiz, Diana a   Louis, Elan D a,b,c   Comella, Cynthia L d   Nance, Martha A e   Bressman, Susan B f,g   Scott, William K h   Tanner, Caroline M i   Mickel, Susan F j   Waters, Cheryl H a   Fahn, Stanley a   Cote, Lucien J a,b   Frucht, Steven J a   Ford, Blair a   Rezak, Michael k   more..


Author keywords

[No Author keywords available]

Indexed keywords

PARKIN; UBIQUITIN PROTEIN LIGASE;

EID: 84892375063     PISSN: 21686149     EISSN: None     Source Type: Journal    
DOI: 10.1001/jamaneurol.2013.4498     Document Type: Article
Times cited : (49)

References (28)
  • 1
    • 0342368772 scopus 로고    scopus 로고
    • Association between early-onset parkinson's disease and mutations in the parkin gene
    • French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease
    • Lücking C.B., Dürr A, Bonifati V., et al.; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. Association between early-onset Parkinson's disease and mutations in the parkin gene. N Engl J Med. 2000; 342(21):1560-1567.
    • (2000) N Engl J Med. , vol.342 , Issue.21 , pp. 1560-1567
    • Lücking, C.B.1    Dürr, A.2    Bonifati, V.3
  • 2
    • 79451474061 scopus 로고    scopus 로고
    • Neuropsychological profile of parkin mutation carriers with and without parkinson disease: The CORE-PD study
    • Caccappolo E, Alcalay RN, Mejia-Santana H, et al Neuropsychological profile of parkin mutation carriers with and without parkinson disease: the CORE-PD study. J Int Neuropsychol Soc. 2011; 17(1):91-100.
    • (2011) J Int Neuropsychol Soc , vol.17 , Issue.1 , pp. 91-100
    • Caccappolo, E.1    Alcalay, R.N.2    Mejia-Santana, H.3
  • 3
    • 60549116319 scopus 로고    scopus 로고
    • A multidisciplinary study of patients with early-onset PD with and without parkin mutations
    • French Parkinson's Disease Genetics Study Group
    • Lohmann E, Thobois S, Lesage S., et al.; French Parkinson's Disease Genetics Study Group. A multidisciplinary study of patients with early-onset PD with and without parkin mutations. Neurology. 2009; 72(2):110-116.
    • (2009) Neurology , vol.72 , Issue.2 , pp. 110-116
    • Lohmann, E.1    Thobois, S.2    Lesage, S.3
  • 4
    • 60549117962 scopus 로고    scopus 로고
    • Parkinson disease(s): Is "Parkin disease" a distinct clinical entity?
    • Klein C, Lohmann K. Parkinson disease(s): is "Parkin disease" a distinct clinical entity? Neurology. 2009; 72(2):106-107.
    • (2009) Neurology , vol.72 , Issue.2 , pp. 106-107
    • Klein, C.1    Lohmann, K.2
  • 5
    • 77957043835 scopus 로고    scopus 로고
    • Frequency of known mutations in early-onset parkinson disease: Implication for genetic counseling: The consortium on risk for early onset parkinson disease study
    • Alcalay RN, Caccappolo E, Mejia-Santana H, et al Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study. Arch Neurol. 2010; 67(9):1116-1122.
    • (2010) Arch Neurol. , vol.67 , Issue.9 , pp. 1116-1122
    • Alcalay, R.N.1    Caccappolo, E.2    Mejia-Santana, H.3
  • 6
    • 77953633735 scopus 로고    scopus 로고
    • Predictors of parkin mutations in early-onset parkinson disease: The consortium on risk for early-onset parkinson disease study
    • Marder KS, Tang MX, Mejia-Santana H, et al Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study. Arch Neurol. 2010; 67(6):731-738.
    • (2010) Arch Neurol. , vol.67 , Issue.6 , pp. 731-738
    • Marder, K.S.1    Tang, M.X.2    Mejia-Santana, H.3
  • 7
    • 68249129262 scopus 로고    scopus 로고
    • Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations
    • Parkinson Study Group-PROGENI Investigators
    • Pankratz N, Kissell DK, Pauciulo M.W., et al.; Parkinson Study Group-PROGENI Investigators. Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations. Neurology. 2009; 73(4):279-286.
    • (2009) Neurology , vol.73 , Issue.4 , pp. 279-286
    • Pankratz, N.1    Kissell, D.K.2    Pauciulo, M.W.3
  • 8
    • 33846833930 scopus 로고    scopus 로고
    • Heterozygous parkin point mutations are as common in control subjects as in parkinson's patients
    • Kay DM, Moran D, Moses L., et al Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients. Ann Neurol. 2007; 61(1):47-54.
    • (2007) Ann Neurol. , vol.61 , Issue.1 , pp. 47-54
    • Kay, D.M.1    Moran, D.2    Moses, L.3
  • 9
    • 33845453622 scopus 로고    scopus 로고
    • Frequency of LRRK2 mutations in early- and late-onset parkinson disease
    • Clark LN, Wang Y, Karlins E., et al Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Neurology. 2006; 67(10):1786-1791.
    • (2006) Neurology , vol.67 , Issue.10 , pp. 1786-1791
    • Clark, L.N.1    Wang, Y.2    Karlins, E.3
  • 10
    • 34548726339 scopus 로고    scopus 로고
    • Mutations in the glucocerebrosidase gene are associated with early-onset parkinson disease
    • Clark LN, Ross BM, Wang Y, et al Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease. Neurology. 2007; 69(12):1270-1277.
    • (2007) Neurology , vol.69 , Issue.12 , pp. 1270-1277
    • Clark, L.N.1    Ross, B.M.2    Wang, Y.3
  • 11
    • 84860708754 scopus 로고    scopus 로고
    • Cognitive performance of GBA mutation carriers with early-onset PD: The CORE-PD study
    • Alcalay RN, Caccappolo E, Mejia-Santana H, et al Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study. Neurology. 2012; 78(18):1434-1440.
    • (2012) Neurology , vol.78 , Issue.18 , pp. 1434-1440
    • Alcalay, R.N.1    Caccappolo, E.2    Mejia-Santana, H.3
  • 12
    • 0000224448 scopus 로고
    • ERMotUDC: The unified parkinson's disease rating scale
    • Fahn S, Marsden CD, Calne DB, Goldstein M, eds. Florham Park, NJ: Macmillan Healthcare Information
    • Fahn S. ERMotUDC: the Unified Parkinson's Disease Rating Scale. In: Fahn S, Marsden CD, Calne DB, Goldstein M, eds. Recent Developments in Parkinson's Disease. Florham Park, NJ: Macmillan Healthcare Information; 1987.
    • (1987) Recent Developments in Parkinson's Disease
    • Fahn, S.1
  • 13
    • 0027425211 scopus 로고
    • The clinical dementia rating (CDR): Current version and scoring rules
    • Morris JC. The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology. 1993; 43(11):2412-2414.
    • (1993) Neurology , vol.43 , Issue.11 , pp. 2412-2414
    • Morris, J.C.1
  • 15
    • 27144549543 scopus 로고    scopus 로고
    • Cognitive profile of patients with newly diagnosed parkinson disease
    • Muslimovic D, Post B, Speelman J.D., Schmand B. Cognitive profile of patients with newly diagnosed Parkinson disease. Neurology. 2005; 65(8):1239-1245.
    • (2005) Neurology , vol.65 , Issue.8 , pp. 1239-1245
    • Muslimovic, D.1    Post, B.2    Speelman, J.D.3    Schmand, B.4
  • 16
    • 0035195760 scopus 로고    scopus 로고
    • Current concepts in mild cognitive impairment
    • Petersen RC, Doody R, Kurz A., et al Current concepts in mild cognitive impairment. Arch Neurol. 2001; 58(12):1985-1992.
    • (2001) Arch Neurol. , vol.58 , Issue.12 , pp. 1985-1992
    • Petersen, R.C.1    Doody, R.2    Kurz, A.3
  • 17
    • 0042415580 scopus 로고    scopus 로고
    • How much phenotypic variation can be attributed to parkin genotype?
    • French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease
    • Lohmann E, Periquet M, Bonifati V., et al.; French Parkinson's Disease Genetics Study Group; European Consortium on Genetic Susceptibility in Parkinson's Disease. How much phenotypic variation can be attributed to parkin genotype? Ann Neurol. 2003; 54(2):176-185.
    • (2003) Ann Neurol. , vol.54 , Issue.2 , pp. 176-185
    • Lohmann, E.1    Periquet, M.2    Bonifati, V.3
  • 18
    • 0038662544 scopus 로고    scopus 로고
    • Parkin disease: A phenotypic study of a large case series
    • Khan NL, Graham E, Critchley P., et al Parkin disease: a phenotypic study of a large case series. Brain. 2003; 126(pt 6):1279-1292.
    • (2003) Brain , vol.126 , Issue.PART 6 , pp. 1279-1292
    • Khan, N.L.1    Graham, E.2    Critchley, P.3
  • 19
    • 0842287328 scopus 로고    scopus 로고
    • Parkin mutation associated parkinsonism and cognitive decline, comparison to early onset parkinson's disease
    • Benbunan BR, Korczyn AD, Giladi N. Parkin mutation associated parkinsonism and cognitive decline, comparison to early onset Parkinson's disease. J Neural Transm. 2004; 111(1):47-57.
    • (2004) J Neural Transm , vol.111 , Issue.1 , pp. 47-57
    • Benbunan, B.R.1    Korczyn, A.D.2    Giladi, N.3
  • 20
    • 0037161261 scopus 로고    scopus 로고
    • Evaluation of 50 probands with early-onset parkinson's disease for parkin mutations
    • Hedrich K, Marder K, Harris J., et al Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations. Neurology. 2002; 58(8):1239-1246.
    • (2002) Neurology , vol.58 , Issue.8 , pp. 1239-1246
    • Hedrich, K.1    Marder, K.2    Harris, J.3
  • 21
    • 61649104022 scopus 로고    scopus 로고
    • Genotypic and phenotypic characteristics of dutch patients with early onset parkinson's disease
    • Macedo MG, Verbaan D, Fang Y., et al Genotypic and phenotypic characteristics of Dutch patients with early onset Parkinson's disease. Mov Disord. 2009; 24(2):196-203.
    • (2009) Mov Disord. , vol.24 , Issue.2 , pp. 196-203
    • Macedo, M.G.1    Verbaan, D.2    Fang, Y.3
  • 22
    • 84859718086 scopus 로고    scopus 로고
    • Clinical and pathological characteristics of LRRK2 G2019S patients with PD
    • Poulopoulos M, Cortes E, Vonsattel J.P., et al Clinical and pathological characteristics of LRRK2 G2019S patients with PD. J Mol Neurosci. 2012; 47(1):139-143.
    • (2012) J Mol Neurosci. , vol.47 , Issue.1 , pp. 139-143
    • Poulopoulos, M.1    Cortes, E.2    Vonsattel, J.P.3
  • 24
    • 84868200922 scopus 로고    scopus 로고
    • Neuropathologic substrates of parkinson disease dementia
    • Irwin DJ, White MT, Toledo J.B., et al Neuropathologic substrates of Parkinson disease dementia. Ann Neurol. 2012; 72(4):587-598.
    • (2012) Ann Neurol. , vol.72 , Issue.4 , pp. 587-598
    • Irwin, D.J.1    White, M.T.2    Toledo, J.B.3
  • 25
    • 79251592293 scopus 로고    scopus 로고
    • Olfaction in parkin heterozygotes and compound heterozygotes: The CORE-PD study
    • Alcalay RN, Siderowf A, Ottman R., et al Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study. Neurology. 2011; 76(4):319-326.
    • (2011) Neurology , vol.76 , Issue.4 , pp. 319-326
    • Alcalay, R.N.1    Siderowf, A.2    Ottman, R.3
  • 26
    • 84897609650 scopus 로고    scopus 로고
    • Knowledge of and interest in genetic results among parkinson disease patients and caregivers
    • [published online June 9, 2013] doi:10.1007/s10897-013-9618-y
    • Sakanaka K, Waters CH, Levy O.A., et al Knowledge of and interest in genetic results among Parkinson disease patients and caregivers [published online June 9, 2013]. J Genet Couns. doi:10.1007/s10897-013-9618-y.
    • J Genet Couns.
    • Sakanaka, K.1    Waters, C.H.2    Levy, O.A.3
  • 27
    • 80052608877 scopus 로고    scopus 로고
    • Genetic testing and parkinson disease: Assessment of patient knowledge, attitudes, and interest
    • Falcone DC, Wood EM, Xie S.X., Siderowf A., Van Deerlin VM. Genetic testing and Parkinson disease: assessment of patient knowledge, attitudes, and interest. J Genet Couns. 2011; 20(4):384-395.
    • (2011) J Genet Couns , vol.20 , Issue.4 , pp. 384-395
    • Falcone, D.C.1    Wood, E.M.2    Xie, S.X.3    Siderowf, A.4    Van Deerlin, V.M.5
  • 28
    • 33748602367 scopus 로고    scopus 로고
    • Genetic testing in parkinson disease: Promises and pitfalls
    • Tan EK, Jankovic J. Genetic testing in Parkinson disease: promises and pitfalls. Arch Neurol. 2006; 63(9):1232-1237.
    • (2006) Arch Neurol. , vol.63 , Issue.9 , pp. 1232-1237
    • Tan, E.K.1    Jankovic, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.