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Current Opinion in Genetics & Development|May 8, 2009
The genetics of Parkinson's syndromes: a critical reviewJohn Hardy, Patrick Lewis, Tamas Revesz, et al.
Neurobiology of Aging|August 9, 2014
Investigating the role of rare coding variability in Mendelian dementia genes (APP, PSEN1, PSEN2, GRN, MAPT, and PRNP) in late-onset Alzheimer's diseaseCeleste Sassi, Rita Guerreiro, Raphael Gibbs, et al.
The Lancet. Neurology|March 17, 2007
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of dataJennifer C Schymick, Sonja W Scholz, Hon-Chung Fung, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 27, 2005
Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year periodJordi Clarimon, Janel Johnson, Ruth Djaldetti, et al.
Trauma Surgery & Acute Care Open|August 31, 2019
Family satisfaction in the trauma and surgical intensive care unit: another important quality measureTom Maxim, Agustin Alvarez, Yvonne Hojberg, et al.
Manual Therapy|June 19, 2016
Association between altered motor control of trunk muscles and head and neck injuries in elite footballers - An exploratory studyJulie A Hides, M Dilani Mendis, Melinda M Franettovich Smith, et al.
The International Journal of Eating Disorders|April 3, 2025
Premature Mortality in Patients With Anorexia Nervosa: A Matched Cohort Study of Cause of DeathNathalie Auger, Mimi Israël, Howard Steiger, et al.
JAMA Psychiatry|October 17, 2019
Association of Bulimia Nervosa With Long-term Risk of Cardiovascular Disease and Mortality Among WomenRasmi M Tith, Gilles Paradis, Brian J Potter, et al.
Immunobiology|August 16, 2011
Complement receptor 1 (CR1) and Alzheimer's diseaseHelen Crehan, Patrick Holton, Selina Wray, et al.
Brain : a Journal of Neurology|April 8, 2017
Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementiaAniket Mishra, Raffaele Ferrari, Peter Heutink, et al.
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