Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity
Dale, Russell C., Church, Andrew J., Surtees, Robert A. H., Lees, Andrew J., Adcock, Jane E., Harding, Brian, Neville, Brian G. R., Giovannoni, Gavin
Published in Brain (London, England : 1878) (01.01.2004)
Published in Brain (London, England : 1878) (01.01.2004)
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Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5′-phosphate oxidase
Mills, Philippa B., Surtees, Robert A.H., Champion, Michael P., Beesley, Clare E., Dalton, Neil, Scambler, Peter J., Heales, Simon J.R., Briddon, Anthony, Scheimberg, Irene, Hoffmann, Georg F., Zschocke, Johannes, Clayton, Peter T.
Published in Human molecular genetics (15.04.2005)
Published in Human molecular genetics (15.04.2005)
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Diagnostic considerations in juvenile parkinsonism
Paviour, Dominic C., Surtees, Robert A.H., Lees, Andrew J.
Published in Movement disorders (01.02.2004)
Published in Movement disorders (01.02.2004)
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Status epilepticus: pathophysiology, epidemiology, and outcomes
Scott, Rod C, Surtees, Robert A H, Neville, Brian G R
Published in Archives of disease in childhood (01.07.1998)
Published in Archives of disease in childhood (01.07.1998)
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Recessively Inherited L-DOPA-Responsive Parkinsonism In Infancy Caused by A Point Mutation (L205p) in the Tyrosine Hydroxylase Gene
Lüdecke, Barbara, Knappskog, Per M., Clayton, Peter T., Surtees, Robert A. H., Clelland, James D., Heales, Simon J. R., Brand, Michael P., Bartholomé, Klaus, Flatmark, Torgeir
Published in Human molecular genetics (01.07.1996)
Published in Human molecular genetics (01.07.1996)
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Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay
de Vries, B B, van'tHoff, W G, Surtees, R A, Winter, R M
Published in Clinical dysmorphology (01.04.2001)
Published in Clinical dysmorphology (01.04.2001)
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