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Movement Disorders : Official Journal of the Movement Disorder Society|September 5, 2002
Genetics of parkinsonismKatrina Gwinn-HardyJournal of Geriatric Psychiatry and Neurology|December 20, 2002
Familial Lewy body diseasesKatrina Gwinn-Hardy, Amanda Adam SingletonMovement Disorders : Official Journal of the Movement Disorder Society|September 3, 2011
Parkinson's disease and α-synuclein expressionMichael J Devine, Katrina Gwinn, Andrew Singleton, et al.Journal of the National Medical Association|July 16, 2004
Prevalence of Parkinson's disease in populations of African ancestry: a reviewAideen McInerney-Leo, Katrina Gwinn-Hardy, Robert L NussbaumMovement Disorders : Official Journal of the Movement Disorder Society|October 27, 2004
Genetic testing in Parkinson's diseaseAideen McInerney-Leo, Donald W Hadley, Katrina Gwinn-Hardy, et al.Annals of Neurology|October 28, 2006
Genetics of Parkinson's disease and parkinsonismJohn Hardy, Huaiban Cai, Mark R Cookson, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 9, 2002
X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?Virgilio Gerald H Evidente, Katrina Gwinn-Hardy, John Hardy, et al.Neurobiology of Disease|March 1, 2006
A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementiaRoneil Malkani, Ian D'Souza, Katrina Gwinn-Hardy, et al.Journal of Neurology|December 14, 2004
Analysis of familial and sporadic restless legs syndrome in age of onset, gender, and severity featuresMelissa Hanson, Melissa Honour, Amanda Singleton, et al.Pageof 7