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Volumn 19, Issue 1, 2009, Pages 69-71

Fahr syndrome, a rare neurodegenerative disorder

Author keywords

Basal ganglia; Calcification; Cerebellum; Fahr's syndrome; Seizure

Indexed keywords

ANTICONVULSIVE AGENT;

EID: 67651177983     PISSN: 10506438     EISSN: None     Source Type: Journal    
DOI: 10.1097/WNQ.0b013e31818d19aa     Document Type: Article
Times cited : (2)

References (13)
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  • 2
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    • Neuropsychological and Neurophysiological features of Fahr's disease
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    • Bobek, J.1    Nowak, M.2
  • 4
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    • Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease)
    • DOI 10.1086/302558
    • Geschwind DH, Loginov M, Stern JM. Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Am J Hum Genet. 1999;65:764-772. (Pubitemid 30468722)
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  • 8
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    • Calcification of the basal ganglia and Fahr disease. Report of two clinical cases and review of the literature
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    • (1993) Recenti Prog Med , vol.84 , pp. 192-198
    • Rossi, M.1    Morena, M.2    Zanardi, M.3
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    • Familial idiopathic cerebral calcifications
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    • (1977) JNNP , vol.40 , pp. 280-285
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  • 10
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    • Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr Disease)
    • Oliviera JR, Spieri E, Sorbido MJ, et al. Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr Disease). Neurology. 2004;63:2165-2167.
    • (2004) Neurology , vol.63 , pp. 2165-2167
    • Oliviera, J.R.1    Spieri, E.2    Sorbido, M.J.3
  • 12
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    • Familial idiopathic brain calcification with autosomal dominant inheritance
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.