Intrafamilial phenotypic variability in idiopathic Fahr’s disease
Downloads
References
Ashtari F, Fatehi F. Fahr's disease: variable presentation in a family. Neurological Sciences 2010; 31:665-7.
Alemdar M, Selek A, Iseri P, Efendi H. Fahr's disease presenting with paroxysmal non-kinesigenic dyskinesia: a case report. Parkinsonism Related Disorders 2008; 14:69-71.
Casanova MF, Araque JM. Mineralization of the basal ganglia: implications for neuropsychiatry, pathology and neuroimaging. Psychiatry Research 2003; 12:159-87.
Hempel A, Henze M, Berghoff C, Garcia N, Ody R, Schroder J.PET findings and neuropsychological deficits in a case of Fahr's disease. Psychiatry Research 2001; 108: 133-40
Le Ber I, Marié RM, Chabot B, Lalevée C, Defer GL. Neuropsychological and 18FDG-PET studies in a family with idiopathic basal ganglia calcifications. Journal of the Neurological Sciences 2007; 258: 115-22.
Wan-Jin Chen et al. Novel SLC20A2 mutations identified in southern Chinese patients with idiopathic basal ganglia. Gene 2013; 529: 159-62.
Dai X., et al. Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification. American Journal of Medical Genetics Part B Neuropsychiatric genetics 2010 ; 153B : 1305-10
