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Items: 1 to 50 of 102

1.

Heat Shock Protein 70 Family Members Interact with Crimean-Congo Hemorrhagic Fever Virus and Hazara Virus Nucleocapsid Proteins and Perform a Functional Role in the Nairovirus Replication Cycle.

Surtees R, Dowall SD, Shaw A, Armstrong S, Hewson R, Carroll MW, Mankouri J, Edwards TA, Hiscox JA, Barr JN.

J Virol. 2016 Sep 29;90(20):9305-16. doi: 10.1128/JVI.00661-16. Print 2016 Oct 15.

2.

The crystal structure of the Hazara virus nucleocapsid protein.

Surtees R, Ariza A, Punch EK, Trinh CH, Dowall SD, Hewson R, Hiscox JA, Barr JN, Edwards TA.

BMC Struct Biol. 2015 Dec 29;15:24. doi: 10.1186/s12900-015-0051-3.

3.

Structure, function, and evolution of the Crimean-Congo hemorrhagic fever virus nucleocapsid protein.

Carter SD, Surtees R, Walter CT, Ariza A, Bergeron É, Nichol ST, Hiscox JA, Edwards TA, Barr JN.

J Virol. 2012 Oct;86(20):10914-23. Epub 2012 Aug 8.

4.

A quantitative proteomic analysis of lung epithelial (A549) cells infected with 2009 pandemic influenza A virus using stable isotope labelling with amino acids in cell culture.

Dove BK, Surtees R, Bean TJ, Munday D, Wise HM, Digard P, Carroll MW, Ajuh P, Barr JN, Hiscox JA.

Proteomics. 2012 May;12(9):1431-6. doi: 10.1002/pmic.201100470. Epub 2012 May 14.

PMID:
22585751
5.

Using SILAC and quantitative proteomics to investigate the interactions between viral and host proteomes.

Munday DC, Surtees R, Emmott E, Dove BK, Digard P, Barr JN, Whitehouse A, Matthews D, Hiscox JA.

Proteomics. 2012 Feb;12(4-5):666-72. doi: 10.1002/pmic.201100488. Epub 2012 Jan 19. Review.

PMID:
22246955
6.

Quantitative proteomic analysis of A549 cells infected with human respiratory syncytial virus.

Munday DC, Emmott E, Surtees R, Lardeau CH, Wu W, Duprex WP, Dove BK, Barr JN, Hiscox JA.

Mol Cell Proteomics. 2010 Nov;9(11):2438-59. doi: 10.1074/mcp.M110.001859. Epub 2010 Jul 20.

7.
9.

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members.

Finch N, Baker M, Crook R, Swanson K, Kuntz K, Surtees R, Bisceglio G, Rovelet-Lecrux A, Boeve B, Petersen RC, Dickson DW, Younkin SG, Deramecourt V, Crook J, Graff-Radford NR, Rademakers R.

Brain. 2009 Mar;132(Pt 3):583-91. doi: 10.1093/brain/awn352. Epub 2009 Jan 21.

10.

Psychogenic movement disorders in children: a report of 15 cases and a review of the literature.

Schwingenschuh P, Pont-Sunyer C, Surtees R, Edwards MJ, Bhatia KP.

Mov Disord. 2008 Oct 15;23(13):1882-8. doi: 10.1002/mds.22280. Review.

PMID:
18759366
11.

'Inductions of labour': on becoming an experienced midwifery practitioner in Aotearoa/New Zealand.

Surtees R.

Nurs Inq. 2008 Mar;15(1):11-20. doi: 10.1111/j.1440-1800.2008.00392.x.

PMID:
18271786
12.

Developing a therapeutic alliance in an eating disorders unit.

Surtees R.

Nurs N Z. 2007 Nov;13(10):14-5. No abstract available.

PMID:
18084966
13.

Cerebroretinal microangiopathy with calcifications and cysts (CRMCC).

Briggs TA, Abdel-Salam GM, Balicki M, Baxter P, Bertini E, Bishop N, Browne BH, Chitayat D, Chong WK, Eid MM, Halliday W, Hughes I, Klusmann-Koy A, Kurian M, Nischal KK, Rice GI, Stephenson JB, Surtees R, Talbot JF, Tehrani NN, Tolmie JL, Toomes C, van der Knaap MS, Crow YJ.

Am J Med Genet A. 2008 Jan 15;146A(2):182-90.

PMID:
18076099
14.
15.

A severity scoring tool to assess the neurological features of neuronopathic Gaucher disease.

Davies EH, Surtees R, DeVile C, Schoon I, Vellodi A.

J Inherit Metab Dis. 2007 Oct;30(5):768-82. Epub 2007 Sep 16. Review.

PMID:
17876722
16.

Changes in postural alignment when using kneeblocks for children with severe motor disorders.

McDonald R, Surtees R.

Disabil Rehabil Assist Technol. 2007 Sep;2(5):287-91.

PMID:
19263534
17.

Treatable neonatal epilepsy.

Surtees R, Wolf N.

Arch Dis Child. 2007 Aug;92(8):659-61. No abstract available.

18.
19.

A standardized tool to measure and describe scleral colour in osteogenesis imperfecta.

Zack P, Zack LR, Surtees R, Neville BG.

Ophthalmic Physiol Opt. 2007 Mar;27(2):174-8.

PMID:
17324207
20.

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
21.

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
22.
23.

Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination.

Wolf NI, Cundall M, Rutland P, Rosser E, Surtees R, Benton S, Chong WK, Malcolm S, Ebinger F, Bitner-Glindzicz M, Woodward KJ.

Neurogenetics. 2007 Jan;8(1):39-44. Epub 2006 Sep 13.

PMID:
16969684
24.

Virchow-Robin spaces on magnetic resonance images: normative data, their dilatation, and a review of the literature.

Groeschel S, Chong WK, Surtees R, Hanefeld F.

Neuroradiology. 2006 Oct;48(10):745-54. Epub 2006 Aug 5. Review.

PMID:
16896908
25.

GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis.

Mercimek-Mahmutoglu S, Stoeckler-Ipsiroglu S, Adami A, Appleton R, Araújo HC, Duran M, Ensenauer R, Fernandez-Alvarez E, Garcia P, Grolik C, Item CB, Leuzzi V, Marquardt I, Mühl A, Saelke-Kellermann RA, Salomons GS, Schulze A, Surtees R, van der Knaap MS, Vasconcelos R, Verhoeven NM, Vilarinho L, Wilichowski E, Jakobs C.

Neurology. 2006 Aug 8;67(3):480-4. Epub 2006 Jul 19.

PMID:
16855203
26.

Pantothenate kinase 2 mutation with classic pantothenate-kinase-associated neurodegeneration without 'eye-of-the-tiger' sign on MRI in a pair of siblings.

Zolkipli Z, Dahmoush H, Saunders DE, Chong WK, Surtees R.

Pediatr Radiol. 2006 Aug;36(8):884-6. Epub 2006 Jun 7.

PMID:
16758184
27.

Influenza virus associated encephalopathy.

Surtees R, DeSousa C.

Arch Dis Child. 2006 Jun;91(6):455-6. No abstract available.

28.

Epilepsy in inborn errors of metabolism.

Wolf NI, Bast T, Surtees R.

Epileptic Disord. 2005 Jun;7(2):67-81. Review.

29.

Disorders of intermediary metabolism: toxic leukoencephalopathies.

Hörster F, Surtees R, Hoffmann GF.

J Inherit Metab Dis. 2005;28(3):345-56. Review.

PMID:
15868467
30.

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
31.

Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher disease.

Wolf NI, Sistermans EA, Cundall M, Hobson GM, Davis-Williams AP, Palmer R, Stubbs P, Davies S, Endziniene M, Wu Y, Chong WK, Malcolm S, Surtees R, Garbern JY, Woodward KJ.

Brain. 2005 Apr;128(Pt 4):743-51. Epub 2005 Feb 2.

PMID:
15689360
32.

Glutaric aciduria type I and kynurenine pathway metabolites: a modified hypothesis.

Varadkar S, Surtees R.

J Inherit Metab Dis. 2004;27(6):835-42. Review.

PMID:
15505390
33.

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.

34.

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
35.

The effect of genotype on the natural history of eIF2B-related leukodystrophies.

Fogli A, Schiffmann R, Bertini E, Ughetto S, Combes P, Eymard-Pierre E, Kaneski CR, Pineda M, Troncoso M, Uziel G, Surtees R, Pugin D, Chaunu MP, Rodriguez D, Boespflug-Tanguy O.

Neurology. 2004 May 11;62(9):1509-17.

PMID:
15136673
36.

Diagnostic considerations in juvenile parkinsonism.

Paviour DC, Surtees RA, Lees AJ.

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

PMID:
14978667
37.

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
38.

Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1.

Pitt M, Houlden H, Jacobs J, Mok Q, Harding B, Reilly M, Surtees R.

Brain. 2003 Dec;126(Pt 12):2682-92. Epub 2003 Sep 23.

PMID:
14506069
39.

A comparison between parents' and therapists' views of their child's individual seating systems.

McDonald R, Surtees R, Wirz S.

Int J Rehabil Res. 2003 Sep;26(3):235-43.

PMID:
14501577
40.

Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable status.

Baxter P, Clarke A, Cross H, Harding B, Hicks E, Livingston J, Surtees R.

Seizure. 2003 Sep;12(6):379-87.

41.
42.

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
43.

Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher disease.

Woodward K, Cundall M, Palmer R, Surtees R, Winter RM, Malcolm S.

Am J Med Genet A. 2003 Apr 1;118A(1):15-24.

PMID:
12605435
44.

L-serine in disease and development.

de Koning TJ, Snell K, Duran M, Berger R, Poll-The BT, Surtees R.

Biochem J. 2003 May 1;371(Pt 3):653-61. Review.

45.

New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.

van der Knaap MS, Naidu S, Pouwels PJ, Bonavita S, van Coster R, Lagae L, Sperner J, Surtees R, Schiffmann R, Valk J.

AJNR Am J Neuroradiol. 2002 Oct;23(9):1466-74.

46.

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
47.

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.

48.

Selective decrease in central nervous system serotonin turnover in children with dopa-nonresponsive dystonia.

Assmann B, Köhler M, Hoffmann GF, Heales S, Surtees R.

Pediatr Res. 2002 Jul;52(1):91-4.

PMID:
12084853
49.

Denaturing gradient gel electrophoresis for the molecular characterization of six patients with guanidinoacetate methyltransferase deficiency.

Item CB, Stromberger C, Mühl A, Edlinger C, Bodamer OA, Schulze A, Surtees R, Leuzzi V, Salomons GS, Jakobs C, Stöckler-Ipsiroglu S.

Clin Chem. 2002 May;48(5):767-9. No abstract available.

50.

Neurological outcome of patients with ornithine carbamoyltransferase deficiency.

Nicolaides P, Liebsch D, Dale N, Leonard J, Surtees R.

Arch Dis Child. 2002 Jan;86(1):54-6.

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