Surtees R - Search Results

1

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. Zolkipli Z, et al. Among authors: surtees r. Pediatr Radiol. 2006 Aug;36(8):884-6. doi: 10.1007/s00247-006-0205-3. Epub 2006 Jun 7. Pediatr Radiol. 2006. PMID: 16758184

2

Painful and painless ophthalmoplegia with cavernous sinus pseudotumour.

Ganesan V, Lin JP, Chong WK, Kirkham FJ, Surtees RA. Ganesan V, et al. Among authors: surtees ra. Arch Dis Child. 1996 Sep;75(3):239-41. doi: 10.1136/adc.75.3.239. Arch Dis Child. 1996. PMID: 8976666 Free PMC article.

3

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. Briggs TA, et al. Among authors: surtees r. Am J Med Genet A. 2008 Jan 15;146A(2):182-90. doi: 10.1002/ajmg.a.32080. Am J Med Genet A. 2008. PMID: 18076099

4

How broad is the phenotype of Hallervorden-Spatz disease?

Hickman SJ, Ward NS, Surtees RA, Stevens JM, Farmer SF. Hickman SJ, et al. Among authors: surtees ra. Acta Neurol Scand. 2001 Mar;103(3):201-3. doi: 10.1034/j.1600-0404.2001.103003201.x. Acta Neurol Scand. 2001. PMID: 11240570

5

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

Assmann B, Köhler M, Hoffmann GF, Heales S, Surtees R. Assmann B, et al. Among authors: surtees r. Pediatr Res. 2002 Jul;52(1):91-4. doi: 10.1203/00006450-200207000-00017. Pediatr Res. 2002. PMID: 12084853

6

Guanidinoacetate methyltransferase deficiency: new clinical features.

Ganesan V, Johnson A, Connelly A, Eckhardt S, Surtees RA. Ganesan V, et al. Among authors: surtees ra. Pediatr Neurol. 1997 Sep;17(2):155-7. doi: 10.1016/s0887-8994(97)00083-0. Pediatr Neurol. 1997. PMID: 9367297

7

Mitochondrial DNA point mutation T9176C in Leigh syndrome.

Wilson CJ, Wood NW, Leonard JV, Surtees R, Rahman S. Wilson CJ, et al. Among authors: surtees r. J Child Neurol. 2000 Dec;15(12):830-3. doi: 10.1177/088307380001501218. J Child Neurol. 2000. PMID: 11198506

8

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. Bandmann O, et al. Among authors: surtees ra. Ann Neurol. 1998 Oct;44(4):649-56. doi: 10.1002/ana.410440411. Ann Neurol. 1998. PMID: 9778264

9

Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.

Bandmann O, Nygaard TG, Surtees R, Marsden CD, Wood NW, Harding AE. Bandmann O, et al. Among authors: surtees r. Hum Mol Genet. 1996 Mar;5(3):403-6. doi: 10.1093/hmg/5.3.403. Hum Mol Genet. 1996. PMID: 8852666

10

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. Wolf NI, et al. Among authors: surtees r. Neurogenetics. 2007 Jan;8(1):39-44. doi: 10.1007/s10048-006-0062-0. Epub 2006 Sep 13. Neurogenetics. 2007. PMID: 16969684

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