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The Journal of Experimental Medicine|June 6, 2007
Complement factor H and the hemolytic uremic syndromeJohn P Atkinson, Timothy H J GoodshipClinical and Experimental Immunology|January 1, 1991
Evidence that X-linked severe combined immunodeficiency is not a differentiation defect of T lymphocytesJ Goodship, S Malcolm, R J LevinskyMovement Disorders : Official Journal of the Movement Disorder Society|June 1, 2011
Parkinson's disease: the quintessential neuropsychiatric disorderDaniel Weintraub, David J BurnJournal of Neurology, Neurosurgery, and Psychiatry|December 17, 1998
Neurology and the kidneyD J Burn, D BatesMovement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
The pathogenesis of multiple system atrophy: past, present, and futureE Jaros, D J BurnLancet (London, England)|August 10, 1999
Left-isomerism sequence and maternal type-1 diabetesM Splitt, C Wright, D Sen, et al.British Medical Bulletin|September 14, 2006
Atypical haemolytic uraemic syndromeDavid Kavanagh, Timothy H J Goodship, Anna RichardsArchives of Disease in Childhood|January 6, 1999
A population study of chromosome 22q11 deletions in infancyJ Goodship, I Cross, J LiLing, et al.Journal of Medical Genetics|May 1, 1990
Unknown syndrome. A possible new X linked retardation syndrome: dysmorphic facies, microcephaly, hypotonia, and small genitaliaM E Porteous, J BurnBiology of the Neonate|January 1, 1976
Isoelectric focusing of non-specific esterases of developing human brain in thin-layer polyacrylamide gelsS S Papiha, J BurnPageof 58