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Molecular Pathology : MP|November 29, 2001
Multiple system atrophy: cellular and molecular pathologyD J Burn, E JarosCytogenetics and Cell Genetics|November 5, 1999
Genetic predictive testing for bowel cancer predisposition: the impact on the individualP D Chapman, J BurnIntensive Care Medicine|July 1, 1978
The effects of insulin glucose administration in fulminant hepatic failureJ Burn, W D WilliamsJournal of Medical Genetics|July 1, 1990
Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasiaJ Goodship, S Malcolm, A Clarke, et al.Scientific Reports|August 6, 2015
Atlantic hurricane activity during the last millenniumMichael J Burn, Suzanne E PalmerCurrent Neurology and Neuroscience Reports|April 30, 2010
Parkinson's disease dementiaMary J Docherty, David J BurnMovement Disorders : Official Journal of the Movement Disorder Society|August 11, 2005
Toward future therapies in progressive supranuclear palsyDavid J Burn, Naomi M WarrenCurrent Opinion in Nephrology and Hypertension|July 10, 2002
The genetics and pathogenesis of haemolytic uraemic syndrome and thrombotic thrombocytopenic purpuraAnna Richards, Judith A Goodship, Timothy H J GoodshipJournal of Medical Genetics|March 1, 1988
Intellectual development in Apert's syndrome: a long term follow up of 29 patientsM A Patton, J Goodship, R Hayward, et al.Pediatric Nephrology (Berlin, Germany)|May 17, 2008
Plasma therapy in atypical haemolytic uremic syndrome: lessons from a family with a factor H mutationJean Claude Davin, Lisa Strain, Tim H J GoodshipPageof 58