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Volumn 24, Issue 1, 2009, Pages 144-147

Pseudo-orthostatic and resting leg tremor in a large Spanish family with homozygous truncating parkin mutation

Author keywords

[No Author keywords available]

Indexed keywords

ALPRAZOLAM; COMPLEMENTARY DNA; LEVODOPA; MESSENGER RNA; PARKIN; TRIHEXYPHENIDYL;

EID: 61449234295     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.22349     Document Type: Article
Times cited : (9)

References (13)
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    • Fast orthostatic tremor in Parkinson's disease mimicking primary orthostatic tremor
    • Apartis E, Tison F, Arne P, Jedynak CP, Vidailhet M. Fast orthostatic tremor in Parkinson's disease mimicking primary orthostatic tremor. Mov Disord 2001;16:1133-1136.
    • (2001) Mov Disord , vol.16 , pp. 1133-1136
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  • 5
    • 30444452091 scopus 로고    scopus 로고
    • Clinical and neurophysiologic spectrum of orthostatic tremor: Case series of 26 subjects
    • Piboolnurak P, Yu QP, Pullman SL. Clinical and neurophysiologic spectrum of orthostatic tremor: case series of 26 subjects. Mov Disord 2005;20:1455-1461.
    • (2005) Mov Disord , vol.20 , pp. 1455-1461
    • Piboolnurak, P.1    Yu, Q.P.2    Pullman, S.L.3
  • 6
    • 34748837001 scopus 로고    scopus 로고
    • Secondary orthostatic tremor in idiopathic Parkinson's disease
    • Mastain B, Cassim F, Guieu JD, Destee A. "Secondary" orthostatic tremor in idiopathic Parkinson's disease. Mov Disord 1998;13 (suppl 144):53.
    • (1998) Mov Disord , vol.13 , Issue.SUPPL. 144 , pp. 53
    • Mastain, B.1    Cassim, F.2    Guieu, J.D.3    Destee, A.4
  • 8
    • 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;126:1279-1292.
    • (2003) Brain , vol.126 , pp. 1279-1292
    • Khan, N.L.1    Graham, E.2    Critchley, P.3
  • 9
    • 0037461335 scopus 로고    scopus 로고
    • New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism
    • Rawal N, Periquet M, Lohmann E, et al. New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism. Neurology 2003;60:1378-1381.
    • (2003) Neurology , vol.60 , pp. 1378-1381
    • Rawal, N.1    Periquet, M.2    Lohmann, E.3
  • 10
    • 2442451698 scopus 로고    scopus 로고
    • Clinical findings in a large family with a parkin Ex3D40 mutation
    • Munhoz RP, Sa DS, Rogaeva E, et al. Clinical findings in a large family with a parkin Ex3D40 mutation. Arch Neurol 2004;61:701-704.
    • (2004) Arch Neurol , vol.61 , pp. 701-704
    • Munhoz, R.P.1    Sa, D.S.2    Rogaeva, E.3
  • 12
    • 33847622175 scopus 로고    scopus 로고
    • Biological effects of the PINK1 c.1366C>T mutation: Implications in Parkinson disease pathogenesis
    • Grünewald A, Breedveld GJ, Lohmann-Hedrich K, et al. Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis. Neurogenetics 2007;8:103-109.
    • (2007) Neurogenetics , vol.8 , pp. 103-109
    • Grünewald, A.1    Breedveld, G.J.2    Lohmann-Hedrich, K.3
  • 13
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    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.