1IshikawaS,Ishikawa M,Tokuda T,et al.Japanese family with anautosomal dominant chromosome inst ability syndrome:a new neuro-degenerative disease[J]Am J Med Genet,2000,94 (4):265-270.
4Ozerov S S,Semen ova ZhB,Zubairaev MS,et al.Concurrence of Fahr's disease with cerebellar tumors[J].Zh Vopr Neirokhir Im N N Burdenko,2004,(4):34-35 ; discussion 35-36.
5Oliveira JR, Spiteri E, Sobrido MJ, et al. Genetic Heterogeneity in Familial Idiopathic Basal Ganglia Cal- cification (Fahr disease) [J]. Neurology (S1526 - 632X),2004,63(11) :2165-2167.
6Geschwind DH, Loginov M, Stern JM. Identification of a Locus on Chromosome 14q for Idiopathic Basal Ganglia Calcification (Fahr Disease)[J]. Am J Hum Genet(S0002- 9297) ,1999,65(3) :764-772.
7Oliveira JR, Sobrido MJ, Spiteri E, et al. Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification ("Fahr's Disease")[J]. J Mol neurosci(S0895 - 8696), 2007,33 (2):151-154.
9Alemdar M, Selek A, Iseri P, et al. Fahr's Disease Presenting with Paroxysmal Non-kinesigenic Dyskinesia: a Case Report [J]. Parkinsonism Relat Disord (S1353- 8020) ,2008,14(1) :69-71.
10Mahy N,Prats A,Riveros A,et al. Basal Ganglia Calcification Induced by Excitotoxicity: an Experimental Model Characterised by Electron Microscopy and X-ray Microanalysis[J]. Aeta Neuropathol ( S0001 - 6322), 1999,98(3) :217-225.