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Items: 32

1.

Rescue of Infectious Recombinant Hazara Nairovirus from cDNA Reveals the Nucleocapsid Protein DQVD Caspase Cleavage Motif Performs an Essential Role other than Cleavage.

Fuller J, Surtees RA, Slack GS, Mankouri J, Hewson R, Barr JN.

J Virol. 2019 Jul 17;93(15). pii: e00616-19. doi: 10.1128/JVI.00616-19. Print 2019 Aug 1.

PMID:
31118258
2.

Hazara nairovirus elicits differential induction of apoptosis and nucleocapsid protein cleavage in mammalian and tick cells.

Fuller J, Surtees RA, Shaw AB, Álvarez-Rodríguez B, Slack GS, Bell-Sakyi L, Mankouri J, Edwards TA, Hewson R, Barr JN.

J Gen Virol. 2019 Mar;100(3):392-402. doi: 10.1099/jgv.0.001211. Epub 2019 Feb 5.

3.

Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I).

Kölker S, Christensen E, Leonard JV, Greenberg CR, Burlina AB, Burlina AP, Dixon M, Duran M, Goodman SI, Koeller DM, Müller E, Naughten ER, Neumaier-Probst E, Okun JG, Kyllerman M, Surtees RA, Wilcken B, Hoffmann GF, Burgard P.

J Inherit Metab Dis. 2007 Feb;30(1):5-22. Epub 2007 Jan 3.

PMID:
17203377
4.

The aetiology of neurological complications of organic acidaemias--a role for the blood-brain barrier.

Kölker S, Sauer SW, Surtees RA, Leonard JV.

J Inherit Metab Dis. 2006 Dec;29(6):701-4; discussion 705-6. Epub 2006 Oct 14.

PMID:
17041745
5.

Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidase.

Mills PB, Surtees RA, Champion MP, Beesley CE, Dalton N, Scambler PJ, Heales SJ, Briddon A, Scheimberg I, Hoffmann GF, Zschocke J, Clayton PT.

Hum Mol Genet. 2005 Apr 15;14(8):1077-86. Epub 2005 Mar 16.

PMID:
15772097
6.

Dyskinesias and associated psychiatric disorders following streptococcal infections.

Dale RC, Heyman I, Surtees RA, Church AJ, Giovannoni G, Goodman R, Neville BG.

Arch Dis Child. 2004 Jul;89(7):604-10.

7.

Infantile Parkinsonism-dystonia and elevated dopamine metabolites in CSF.

Assmann BE, Robinson RO, Surtees RA, Bräutigam C, Heales SJ, Wevers RA, Zschocke J, Hyland K, Sharma R, Hoffmann GF.

Neurology. 2004 May 25;62(10):1872-4.

PMID:
15159499
8.

Diagnostic considerations in juvenile parkinsonism.

Paviour DC, Surtees RA, Lees AJ.

Mov Disord. 2004 Feb;19(2):123-35. Review.

PMID:
14978667
9.

Encephalitis lethargica syndrome: 20 new cases and evidence of basal ganglia autoimmunity.

Dale RC, Church AJ, Surtees RA, Lees AJ, Adcock JE, Harding B, Neville BG, Giovannoni G.

Brain. 2004 Jan;127(Pt 1):21-33. Epub 2003 Oct 21.

PMID:
14570817
10.

Neonatal epileptic encephalopathy.

Clayton PT, Surtees RA, DeVile C, Hyland K, Heales SJ.

Lancet. 2003 May 10;361(9369):1614. No abstract available.

PMID:
12747882
11.

Post-streptococcal autoimmune neuropsychiatric disease presenting as paroxysmal dystonic choreoathetosis.

Dale RC, Church AJ, Surtees RA, Thompson EJ, Giovannoni G, Neville BG.

Mov Disord. 2002 Jul;17(4):817-20.

PMID:
12210883
12.

Post-streptococcal autoimmune dystonia with isolated bilateral striatal necrosis.

Dale RC, Church AJ, Benton S, Surtees RA, Lees A, Thompson EJ, Giovannoni G, Neville BG.

Dev Med Child Neurol. 2002 Jul;44(7):485-9.

13.

Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delay.

de Vries BB, van'tHoff WG, Surtees RA, Winter RM.

Clin Dysmorphol. 2001 Apr;10(2):115-21.

PMID:
11310991
14.

How broad is the phenotype of Hallervorden-Spatz disease?

Hickman SJ, Ward NS, Surtees RA, Stevens JM, Farmer SF.

Acta Neurol Scand. 2001 Mar;103(3):201-3.

PMID:
11240570
15.

Liver transplantation for methylmalonic acidaemia.

van't Hoff W, McKiernan PJ, Surtees RA, Leonard JV.

Eur J Pediatr. 1999 Dec;158 Suppl 2:S70-4.

PMID:
10603103
17.

Dopa-responsive dystonia: a clinical and molecular genetic study.

Bandmann O, Valente EM, Holmans P, Surtees RA, Walters JH, Wevers RA, Marsden CD, Wood NW.

Ann Neurol. 1998 Oct;44(4):649-56.

PMID:
9778264
18.

Status epilepticus: pathophysiology, epidemiology, and outcomes.

Scott RC, Surtees RA, Neville BG.

Arch Dis Child. 1998 Jul;79(1):73-7. Review. No abstract available.

19.

Cerebrospinal fluid investigations for neurometabolic disorders.

Hoffmann GF, Surtees RA, Wevers RA.

Neuropediatrics. 1998 Apr;29(2):59-71. Review.

PMID:
9638660
20.

Clinical outcomes in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

Morris AA, Clayton PT, Surtees RA, Leonard JV.

J Pediatr. 1997 Dec;131(6):938. No abstract available.

PMID:
9427908
21.

Guanidinoacetate methyltransferase deficiency: new clinical features.

Ganesan V, Johnson A, Connelly A, Eckhardt S, Surtees RA.

Pediatr Neurol. 1997 Sep;17(2):155-7.

PMID:
9367297
23.

Painful and painless ophthalmoplegia with cavernous sinus pseudotumour.

Ganesan V, Lin JP, Chong WK, Kirkham FJ, Surtees RA.

Arch Dis Child. 1996 Sep;75(3):239-41.

24.

Recessively inherited L-DOPA-responsive parkinsonism in infancy caused by a point mutation (L205P) in the tyrosine hydroxylase gene.

Lüdecke B, Knappskog PM, Clayton PT, Surtees RA, Clelland JD, Heales SJ, Brand MP, Bartholomé K, Flatmark T.

Hum Mol Genet. 1996 Jul;5(7):1023-8.

PMID:
8817341
25.

Age dependent changes in the cerebrospinal fluid concentration of nitrite and nitrate.

Clelland JD, Brand MP, Bolaños JP, Surtees RA, Land JM, Heales SJ.

Ann Clin Biochem. 1996 Jan;33 ( Pt 1):71-2. No abstract available.

PMID:
8929071
26.

Cerebrospinal fluid concentrations of pterins and metabolites of serotonin and dopamine in a pediatric reference population.

Hyland K, Surtees RA, Heales SJ, Bowron A, Howells DW, Smith I.

Pediatr Res. 1993 Jul;34(1):10-4.

PMID:
7689195
27.

Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers.

Haworth JC, Dilling LA, Surtees RA, Seargeant LE, Lue-Shing H, Cooper BA, Rosenblatt DS.

Am J Med Genet. 1993 Mar 1;45(5):572-6.

PMID:
8456826
28.
29.

Neurologic outcome of propionic acidemia.

Surtees RA, Matthews EE, Leonard JV.

Pediatr Neurol. 1992 Sep-Oct;8(5):333-7.

PMID:
1418175
30.

The role of growth hormone in stunted head growth after cranial irradiation.

Clayton PE, Shalet SM, Price DA, Surtees RA, Pearson D.

Pediatr Res. 1987 Oct;22(4):402-4.

PMID:
3684370
31.

Seasonal variation of glycosylated haemoglobin.

Ferrie CD, Sharpe TC, Price DA, Surtees RA.

Arch Dis Child. 1987 Sep;62(9):959-60.

32.

Growth hormone deficiency in one of identical twins.

Surtees RA, Price DA.

Acta Paediatr Scand. 1987 Sep;76(5):837-8. No abstract available.

PMID:
3661188

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