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Annals of Neurology|March 23, 2001
Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin geneR Hilker, C Klein, M Ghaemi, et al.Journal of Medical Genetics|September 1, 1987
DNA linkage analysis in Von Recklinghausen neurofibromatosisB R Seizinger, G Rouleau, A H Lane, et al.Annals of Neurology|November 1, 1994
Dystonia in Ashkenazi Jews: clinical characterization of a founder mutationS B Bressman, D de Leon, P L Kramer, et al.Neurology|July 15, 2011
Olfactory dysfunction in LRRK2 G2019S mutation carriersR Saunders-Pullman, K Stanley, C Wang, et al.American Journal of Human Genetics|September 1, 1994
The DYT1 gene on 9q34 is responsible for most cases of early limb-onset idiopathic torsion dystonia in non-JewsP L Kramer, G A Heiman, T Gasser, et al.Neurology|June 1, 1997
Secondary dystonia and the DYTI geneS B Bressman, D de Leon, D Raymond, et al.Nature Genetics|June 1, 1993
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosisA Blumenfeld, S A Slaugenhaupt, F B Axelrod, et al.Journal of Medical Genetics|January 1, 1993
Exclusion of familial dysautonomia from more than 60% of the genomeA Blumenfeld, F B Axelrod, J A Trofatter, et al.Neurology|December 11, 2002
Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystoniaC Klein, K Hedrich, K Kabakçi, et al.Neurology|January 24, 2002
Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependenceR Saunders-Pullman, J Shriberg, G Heiman, et al.Pageof 7