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Volumn 23, Issue 7, 2008, Pages 807-809

Juvenile Huntington disease exacerbated by methylphenidate: Case report

Author keywords

Attention deficit; Basal ganglia; Huntington disease

Indexed keywords

ADENOSINE; CYTOSINE; DOPAMINE RECEPTOR STIMULATING AGENT; GUANINE; METHYLPHENIDATE;

EID: 47349132531     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/0883073808314152     Document Type: Article
Times cited : (18)

References (19)
  • 1
    • 12144288251 scopus 로고    scopus 로고
    • Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset
    • Wexler NS, Lorimer J., Porter J., et al. Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset. Proc Natl Acad Sci U S A. 2004; 101:3498-3503.
    • (2004) Proc Natl Acad Sci U S A , vol.101 , pp. 3498-3503
    • Wexler, N.S.1    Lorimer, J.2    Porter, J.3
  • 2
    • 33745174181 scopus 로고    scopus 로고
    • Clinical characteristics of childhood-onset (juvenile) Huntington disease: Report of 12 patients and review of the literature
    • Gonzalez-Alegre P., Afifi AK Clinical characteristics of childhood-onset (juvenile) Huntington disease: Report of 12 patients and review of the literature. J Child Neurol. 2006; 21:223-229.
    • (2006) J Child Neurol. , vol.21 , pp. 223-229
    • Gonzalez-Alegre, P.1    Afifi, A.K.2
  • 3
    • 0033771298 scopus 로고    scopus 로고
    • Huntington disease in children: Genotype-phenotype correlation
    • Rasmussen A., Macias R., Yescas P., et al. Huntington disease in children: Genotype-phenotype correlation. Neuropediatrics. 2000; 31:190-194.
    • (2000) Neuropediatrics , vol.31 , pp. 190-194
    • Rasmussen, A.1    Macias, R.2    Yescas, P.3
  • 4
    • 33749854930 scopus 로고    scopus 로고
    • Speech and language delay are early manifestations of juvenile-onset Huntington disease
    • Yoon G., Kramer J., Zanko A., et al. Speech and language delay are early manifestations of juvenile-onset Huntington disease. Neurology. 2006; 67:1265-1267.
    • (2006) Neurology , vol.67 , pp. 1265-1267
    • Yoon, G.1    Kramer, J.2    Zanko, A.3
  • 6
    • 11244324114 scopus 로고    scopus 로고
    • Early onset Huntington disease: A neuronal degeneration syndrome
    • Seneca S., Fagnart D., Keymolen K., et al. Early onset Huntington disease: A neuronal degeneration syndrome. Eur J Pediatr. 2004; 163:717-721.
    • (2004) Eur J Pediatr. , vol.163 , pp. 717-721
    • Seneca, S.1    Fagnart, D.2    Keymolen, K.3
  • 7
    • 33847195685 scopus 로고    scopus 로고
    • Huntington's disease presenting as a depressive disorder with psychotic features
    • Jardri R., Medjkane F., Cuisset JM, et al. Huntington's disease presenting as a depressive disorder with psychotic features. J Am Acad Child Adolesc Psychiatry. 2007; 46:307-308.
    • (2007) J Am Acad Child Adolesc Psychiatry , vol.46 , pp. 307-308
    • Jardri, R.1    Medjkane, F.2    Cuisset, J.M.3
  • 8
    • 0027176364 scopus 로고
    • The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
    • Andrew SE, Goldberg YP, Kremer B., et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease. Nat Genet. 1993; 4:398-403.
    • (1993) Nat Genet. , vol.4 , pp. 398-403
    • Andrew, S.E.1    Goldberg, Y.P.2    Kremer, B.3
  • 9
    • 1842477303 scopus 로고    scopus 로고
    • A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length
    • Langbehn DR, Brinkman RR, Falush D., et al. A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length. Clin Genet. 2004; 65:267-277.
    • (2004) Clin Genet. , vol.65 , pp. 267-277
    • Langbehn, D.R.1    Brinkman, R.R.2    Falush, D.3
  • 10
    • 0035827818 scopus 로고    scopus 로고
    • Familial influence on age of onset among siblings with Huntington disease
    • Rosenblatt A., Brinkman RR, Liang KY, et al. Familial influence on age of onset among siblings with Huntington disease. Am J Med Genet. 2001; 105:399-403.
    • (2001) Am J Med Genet. , vol.105 , pp. 399-403
    • Rosenblatt, A.1    Brinkman, R.R.2    Liang, K.Y.3
  • 11
    • 0033022687 scopus 로고    scopus 로고
    • Differences in duration of Huntington's disease based on age at onset
    • Foroud T., Gray J., Ivashina J., et al. Differences in duration of Huntington's disease based on age at onset. J Neurol Neurosurg Psychiatry. 1999; 66:52-56.
    • (1999) J Neurol Neurosurg Psychiatry , vol.66 , pp. 52-56
    • Foroud, T.1    Gray, J.2    Ivashina, J.3
  • 12
    • 33646085784 scopus 로고    scopus 로고
    • The association of CAG repeat length with clinical progression in Huntington disease
    • Rosenblatt A., Liang KY, Zhou H., et al. The association of CAG repeat length with clinical progression in Huntington disease. Neurology. 2006; 66:1016-1020.
    • (2006) Neurology , vol.66 , pp. 1016-1020
    • Rosenblatt, A.1    Liang, K.Y.2    Zhou, H.3
  • 13
    • 33646022550 scopus 로고    scopus 로고
    • The search for cerebral biomarkers of Huntington's disease: A review of genetic models of age at onset prediction
    • Squitieri F., Ciarmiello A., Di Donato S., et al. The search for cerebral biomarkers of Huntington's disease: A review of genetic models of age at onset prediction. Eur J Neurol. 2006; 13:408-415.
    • (2006) Eur J Neurol. , vol.13 , pp. 408-415
    • Squitieri, F.1    Ciarmiello, A.2    Di Donato, S.3
  • 14
    • 33749416817 scopus 로고    scopus 로고
    • Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: The HD MAPS study
    • Li JL, Hayden MR, Warby SC, et al. Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: The HD MAPS study. BMC Med Genet. 2006; 7: 71.
    • (2006) BMC Med Genet. , vol.7 , pp. 71
    • Li, J.L.1    Hayden, M.R.2    Warby, S.C.3
  • 15
    • 0030851715 scopus 로고    scopus 로고
    • Side effects of methylphenidate and dexamphetamine in children with attention deficit hyperactivity disorder: A double-blind, crossover trial
    • Efron D., Jarman F., Barker M. Side effects of methylphenidate and dexamphetamine in children with attention deficit hyperactivity disorder: A double-blind, crossover trial. Pediatrics. 1997; 100:662-666.
    • (1997) Pediatrics , vol.100 , pp. 662-666
    • Efron, D.1    Jarman, F.2    Barker, M.3
  • 16
    • 0030773501 scopus 로고    scopus 로고
    • Methylphenidate and brain dopamine neurotoxicity
    • Yuan J., McCann U., Ricaurte G. Methylphenidate and brain dopamine neurotoxicity. Brain Res. 1997; 767:172-175.
    • (1997) Brain Res. , vol.767 , pp. 172-175
    • Yuan, J.1    McCann, U.2    Ricaurte, G.3
  • 17
    • 33845612662 scopus 로고    scopus 로고
    • Dopamine enhances motor and neuropathological consequences of polyglutamine expanded huntingtin
    • Cyr M., Sotnikova TD, Gainetdinov RR, et al. Dopamine enhances motor and neuropathological consequences of polyglutamine expanded huntingtin. FASEB J. 2006; 20:2541-2543.
    • (2006) FASEB J , vol.20 , pp. 2541-2543
    • Cyr, M.1    Sotnikova, T.D.2    Gainetdinov, R.R.3
  • 18
    • 0018827748 scopus 로고
    • Levodopa and presymptomatic detection of Huntington's disease-eight-year follow-up
    • Klawans HL, Goetz CG, Paulson GW, et al. Levodopa and presymptomatic detection of Huntington's disease-eight-year follow-up. N Engl J Med. 1980; 302:1090.
    • (1980) N Engl J Med. , vol.302 , pp. 1090
    • Klawans, H.L.1    Goetz, C.G.2    Paulson, G.W.3
  • 19
    • 0028115834 scopus 로고
    • Paroxysmal kinesigenic dystonia after methylphenidate administration
    • Gay CT, Ryan SG Paroxysmal kinesigenic dystonia after methylphenidate administration. J Child Neurol. 1994; 9:45-46.
    • (1994) J Child Neurol. , vol.9 , pp. 45-46
    • Gay, C.T.1    Ryan, S.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.