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Journal of Neurology
Volumn 253, Issue 2, 2006, Pages 261-262
Hereditary hemochromatosis and movement disorders: The still controversial relationship - Response to Russo et al. in J Neurol (2004) 251:849-852 [6]
Author keywords

[No Author keywords available]
Indexed keywords

CHOREA; CONFIDENCE INTERVAL; DYSTONIA; GAIT DISORDER; GENE LOCUS; GENE MUTATION; HEMOCHROMATOSIS; HOMOZYGOSITY; HUMAN; HUNTINGTON CHOREA; LETTER; MOTOR DYSFUNCTION; PARKINSON DISEASE; PRIORITY JOURNAL;
EID: 32844459070     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-005-0954-1     Document Type: Letter
Times cited : (2)
References (8)
  • 1
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    • Hereditary haemochromatosis is unlikely to cause movement disorders. A critical review
    • Russo N, Edwards M, Andrews T, O'Brien M, Bhatia KP (2004) Hereditary haemochromatosis is unlikely to cause movement disorders. A critical review. J Neurol 251:849-852
    • (2004) J Neurol , vol.251 , pp. 849-852
    • Russo, N.1    Edwards, M.2    Andrews, T.3    O'Brien, M.4    Bhatia, K.P.5
  • 2
    • 0033709765 scopus 로고    scopus 로고
    • Clinical report of three patients with hereditary hemochromatosis and movement disorders
    • Demarquay G, Setiey A, Morel Y, Trepo C, Chazot G, Broussolle E (2000) Clinical report of three patients with hereditary hemochromatosis and movement disorders. Mov Disord 15:1204-1209
    • (2000) Mov Disord , vol.15 , pp. 1204-1209
    • Demarquay, G.1    Setiey, A.2    Morel, Y.3    Trepo, C.4    Chazot, G.5    Broussolle, E.6
  • 3
    • 0021035887 scopus 로고
    • Idiopathic hemochromatosis (IHC): Dementia and ataxia as presenting signs
    • Jones HR Jr, Hedley-Whyte ET (1983) Idiopathic hemochromatosis (IHC): dementia and ataxia as presenting signs. Neurology 33:1479-1483
    • (1983) Neurology , vol.33 , pp. 1479-1483
    • Jones Jr., H.R.1    Hedley-Whyte, E.T.2
  • 4
    • 0023162154 scopus 로고
    • Extrapyramidal syndrome in idiopathic hemochromatosis. Significance of laboratory chemical, neurophysiologic and imaging procedures
    • Schröder J, Haan J (1987) Extrapyramidal syndrome in idiopathic hemochromatosis. Significance of laboratory chemical, neurophysiologic and imaging procedures. Nervenarzt 58:577-578
    • (1987) Nervenarzt , vol.58 , pp. 577-578
    • Schröder, J.1    Haan, J.2
  • 5
    • 0029086742 scopus 로고
    • Hereditary haemochromatosis: A case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome
    • Nielsen JE, Neerup Jensen L, Krabbe K (1995) Hereditary haemochromatosis: a case of iron accumulation in the basal ganglia associated with a parkinsonian syndrome. J Neurol Neurosurg Psychiatry 59:318-321
    • (1995) J Neurol Neurosurg Psychiatry , vol.59 , pp. 318-321
    • Nielsen, J.E.1    Neerup Jensen, L.2    Krabbe, K.3
  • 6
    • 1642564597 scopus 로고    scopus 로고
    • Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: A case report series
    • Costello DJ, Walsh SL, Harrington HJ, Walsh CH (2004) Concurrent hereditary haemochromatosis and idiopathic Parkinson's disease: a case report series. J Neurol Neurosurg Psychiatry 75:631-633
    • (2004) J Neurol Neurosurg Psychiatry , vol.75 , pp. 631-633
    • Costello, D.J.1    Walsh, S.L.2    Harrington, H.J.3    Walsh, C.H.4
  • 7
    • 0036266999 scopus 로고    scopus 로고
    • High headache prevalence among women with hemochromatosis: The Nord-Trondelag health study
    • Hagen K, Stovner LJ, Asberg A, Thorstensen K, Bjerve KS, Hveem K (2002) High headache prevalence among women with hemochromatosis: the Nord-Trondelag health study. Ann Neurol 51:786-789
    • (2002) Ann Neurol , vol.51 , pp. 786-789
    • Hagen, K.1    Stovner, L.J.2    Asberg, A.3    Thorstensen, K.4    Bjerve, K.S.5    Hveem, K.6

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.