PubMed

Eicosanoid involvement in the regulation of behavioral fever in the desert locust, Schistocerca gregaria.

Bundey S, Raymond S, Dean P, Roberts SK, Dillon RJ, Charnley AK.

Arch Insect Biochem Physiol. 2003 Apr;52(4):183-92.PMID: 12655606 [PubMed - indexed for MEDLINE]Related articles

Assessment of cannabinoid induced gene changes: tolerance and neuroprotection.

Grigorenko E, Kittler J, Clayton C, Wallace D, Zhuang S, Bridges D, Bundey S, Boon A, Pagget C, Hayashizaki S, Lowe G, Hampson R, Deadwyler S.

Chem Phys Lipids. 2002 Dec 31;121(1-2):257-66. Review.PMID: 12505705 [PubMed - indexed for MEDLINE]Related articles

Rufous albinism.

Mehta JS, Good P, Maharaj D, Butler L, Bundey S, O'Shea J.

J Pediatr Ophthalmol Strabismus. 2001 Mar-Apr;38(2):117-9. No abstract available. PMID: 11310706 [PubMed - indexed for MEDLINE]Related articles

Large-scale analysis of gene expression changes during acute and chronic exposure to [Delta]9-THC in rats.

Kittler JT, Grigorenko EV, Clayton C, Zhuang SY, Bundey SC, Trower MM, Wallace D, Hampson R, Deadwyler S.

Physiol Genomics. 2000 Sep 8;3(3):175-85.PMID: 11015613 [PubMed - indexed for MEDLINE]Related articles

A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.

Liu XZ, Hope C, Liang CY, Zou JM, Xu LR, Cole T, Mueller RF, Bundey S, Nance W, Steel KP, Brown SD.

Am J Hum Genet. 1999 Apr;64(4):1221-5. No abstract available. PMID: 10090909 [PubMed - indexed for MEDLINE]Related articlesFree article

A gene for autosomal recessive symmetrical spastic cerebral palsy maps to chromosome 2q24-25.

McHale DP, Mitchell S, Bundey S, Moynihan L, Campbell DA, Woods CG, Lench NJ, Mueller RF, Markham AF.

Am J Hum Genet. 1999 Feb;64(2):526-32.PMID: 9973289 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

Liu XZ, Hope C, Walsh J, Newton V, Ke XM, Liang CY, Xu LR, Zhou JM, Trump D, Steel KP, Bundey S, Brown SD.

Am J Hum Genet. 1998 Sep;63(3):909-12. No abstract available. PMID: 9718356 [PubMed - indexed for MEDLINE]Related articlesFree article

A comparison of disease and gene frequencies of inborn errors of metabolism among different ethnic groups in the West Midlands, UK.

Hutchesson AC, Bundey S, Preece MA, Hall SK, Green A.

J Med Genet. 1998 May;35(5):366-70.PMID: 9610798 [PubMed - indexed for MEDLINE]Related articlesFree article

Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.

Moynihan LM, Bundey SE, Heath D, Jones EL, McHale DP, Mueller RF, Markham AF, Lench NJ.

Am J Hum Genet. 1998 May;62(5):1123-8.PMID: 9545394 [PubMed - indexed for MEDLINE]Related articlesFree article

A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24.

Mitchell SJ, McHale DP, Campbell DA, Lench NJ, Mueller RF, Bundey SE, Markham AF.

Am J Hum Genet. 1998 May;62(5):1070-6.PMID: 9545391 [PubMed - indexed for MEDLINE]Related articlesFree article

Wolfram (DIDMOAD) syndrome.

Barrett TG, Bundey SE.

J Med Genet. 1997 Oct;34(10):838-41. Review.PMID: 9350817 [PubMed - indexed for MEDLINE]Related articlesFree article

'Prevalence and type of cerebral palsy'.

Bundey S.

Dev Med Child Neurol. 1997 Aug;39(8):568. No abstract available. PMID: 9295856 [PubMed - indexed for MEDLINE]Related articles

A novel mechanism of aberrant pre-mRNA splicing in humans.

Cogan JD, Prince MA, Lekhakula S, Bundey S, Futrakul A, McCarthy EM, Phillips JA 3rd.

Hum Mol Genet. 1997 Jun;6(6):909-12.PMID: 9175738 [PubMed - indexed for MEDLINE]Related articlesFree article

Few psychological consequences of presymptomatic testing for Huntington disease.

Bundey S.

Lancet. 1997 Jan 4;349(9044):4. No abstract available. PMID: 8988110 [PubMed - indexed for MEDLINE]Related articles

Optic atrophy in Wolfram (DIDMOAD) syndrome.

Barrett TG, Bundey SE, Fielder AR, Good PA.

Eye (Lond). 1997;11 ( Pt 6):882-8.PMID: 9537152 [PubMed - indexed for MEDLINE]Related articles

Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Hope CI, Bundey S, Proops D, Fielder AR.

Br J Ophthalmol. 1997 Jan;81(1):46-53.PMID: 9135408 [PubMed - indexed for MEDLINE]Related articlesFree article

Symmetry of neurological signs in Pakistani patients with probable inherited spastic cerebral palsy.

Mitchell S, Bundey S.

Clin Genet. 1997 Jan;51(1):7-14.PMID: 9084927 [PubMed - indexed for MEDLINE]Related articles

Fragile X syndrome is less common than previously estimated.

Morton JE, Bundey S, Webb TP, MacDonald F, Rindl PM, Bullock S.

J Med Genet. 1997 Jan;34(1):1-5.PMID: 9032640 [PubMed - indexed for MEDLINE]Related articlesFree article

Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneity.

Collier DA, Barrett TG, Curtis D, Macleod A, Arranz MJ, Maassen JA, Bundey S.

Am J Hum Genet. 1996 Oct;59(4):855-63.PMID: 8808601 [PubMed - indexed for MEDLINE]Related articlesFree article

Julia Bell (1879-1979). Steamboat Lady, statistician and geneticist.

Bundey S.

J Med Biogr. 1996 Feb;4(1):8-13. No abstract available. PMID: 11615351 [PubMed - indexed for MEDLINE]Related articles

ERG and EOG abnormalities in carriers of X-linked retinitis pigmentosa.

Stavrou P, Good PA, Broadhurst EJ, Bundey S, Fielder AR, Crews SJ.

Eye (Lond). 1996;10 ( Pt 5):581-9.PMID: 8977786 [PubMed - indexed for MEDLINE]Related articles

The representation of ethnic minorities at genetic clinics in Birmingham.

Roberts A, Cullen R, Bundey S.

J Med Genet. 1996 Jan;33(1):56-8.PMID: 8825050 [PubMed - indexed for MEDLINE]Related articlesFree article

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

Barrett TG, Bundey SE, Macleod AF.

Lancet. 1995 Dec 2;346(8988):1458-63.PMID: 7490992 [PubMed - indexed for MEDLINE]Related articles

A clinical and molecular genetic study of dentatorubropallidoluysian atrophy in four European families.

Warner TT, Williams LD, Walker RW, Flinter F, Robb SA, Bundey SE, Honavar M, Harding AE.

Ann Neurol. 1995 Apr;37(4):452-9.PMID: 7717681 [PubMed - indexed for MEDLINE]Related articles

DIDMOAD syndrome; further studies and muscle biochemistry.

Barrett TG, Poulton K, Bundey S.

J Inherit Metab Dis. 1995;18(2):218-20. No abstract available. PMID: 7564251 [PubMed - indexed for MEDLINE]Related articles

Clinical and genetic features of ataxia-telangiectasia.

Bundey S.

Int J Radiat Biol. 1994 Dec;66(6 Suppl):S23-9. Review.PMID: 7836849 [PubMed - indexed for MEDLINE]Related articles

Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

Aldred MA, Teague PW, Jay M, Bundey S, Redmond RM, Jay B, Bird AC, Bhattacharya SS, Wright AF.

J Med Genet. 1994 Nov;31(11):848-52.PMID: 7853368 [PubMed - indexed for MEDLINE]Related articlesFree article

X inactivation patterns in female monozygotic twins and their families.

Watkiss E, Webb T, Rysiecki G, Girdler N, Hewett E, Bundey S.

J Med Genet. 1994 Oct;31(10):754-7.PMID: 7837250 [PubMed - indexed for MEDLINE]Related articlesFree article

Duplication of the 15q11-13 region in a patient with autism, epilepsy and ataxia.

Bundey S, Hardy C, Vickers S, Kilpatrick MW, Corbett JA.

Dev Med Child Neurol. 1994 Aug;36(8):736-42.PMID: 8050626 [PubMed - indexed for MEDLINE]Related articles

Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinism.

Lee ST, Nicholls RD, Bundey S, Laxova R, Musarella M, Spritz RA.

N Engl J Med. 1994 Feb 24;330(8):529-34.PMID: 8302318 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA).

Tripathi RK, Bundey S, Musarella MA, Droetto S, Strunk KM, Holmes SA, Spritz RA.

Am J Hum Genet. 1993 Dec;53(6):1173-9.PMID: 7902671 [PubMed - indexed for MEDLINE]Related articlesFree article

Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene.

Sweeney MG, Bundey S, Brockington M, Poulton KR, Winer JB, Harding AE.

Q J Med. 1993 Nov;86(11):709-13.PMID: 8265770 [PubMed - indexed for MEDLINE]Related articles

Wolfram syndrome: mitochondrial disorder.

Bundey S, Fielder A, Poulton K.

Lancet. 1993 Oct 23;342(8878):1059-60. No abstract available. PMID: 8105296 [PubMed - indexed for MEDLINE]Related articles

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.

Chen ZY, Battinelli EM, Fielder A, Bundey S, Sims K, Breakefield XO, Craig IW.

Nat Genet. 1993 Oct;5(2):180-3.PMID: 8252044 [PubMed - indexed for MEDLINE]Related articles

Is skewed X inactivation responsible for symptoms in female carriers for adrenoleucodystrophy?

Watkiss E, Webb T, Bundey S.

J Med Genet. 1993 Aug;30(8):651-4.PMID: 8411051 [PubMed - indexed for MEDLINE]Related articlesFree article

Low segregation ratios in autosomal recessive disorders.

Bundey S, Young ID.

J Med Genet. 1993 Jun;30(6):449-51. No abstract available. PMID: 8179645 [PubMed - indexed for MEDLINE]Related articlesFree article

Population screening for fragile-X syndrome.

Bundey S, Norman E.

Lancet. 1993 Mar 20;341(8847):770. No abstract available. PMID: 8095682 [PubMed - indexed for MEDLINE]Related articles

X linked exudative vitreoretinopathy: clinical features and genetic linkage analysis.

Fullwood P, Jones J, Bundey S, Dudgeon J, Fielder AR, Kilpatrick MW.

Br J Ophthalmol. 1993 Mar;77(3):168-70.PMID: 8457509 [PubMed - indexed for MEDLINE]Related articlesFree article

A five-year prospective study of the health of children in different ethnic groups, with particular reference to the effect of inbreeding.

Bundey S, Alam H.

Eur J Hum Genet. 1993;1(3):206-19.PMID: 8044647 [PubMed - indexed for MEDLINE]Related articles

Racial distribution of Duchenne muscular dystrophy in the West Midlands region of Britain.

Roddie A, Bundey S.

J Med Genet. 1992 Aug;29(8):555-7.PMID: 1518024 [PubMed - indexed for MEDLINE]Related articlesFree article

Multiple mutation in an extended Duchenne muscular dystrophy family.

Miciak A, Keen A, Jadayel D, Bundey S.

J Med Genet. 1992 Feb;29(2):123-6.PMID: 1351947 [PubMed - indexed for MEDLINE]Related articlesFree article

Mitochondrial abnormalities in the DIDMOAD syndrome.

Bundey S, Poulton K, Whitwell H, Curtis E, Brown IA, Fielder AR.

J Inherit Metab Dis. 1992;15(3):315-9. No abstract available. PMID: 1383603 [PubMed - indexed for MEDLINE]Related articles

Uses and limitations of twin studies.

Bundey S.

J Neurol. 1991 Oct;238(7):360-4.PMID: 1960539 [PubMed - indexed for MEDLINE]Related articles

Allan-Herndon syndrome--or X-linked cerebral palsy?

Bundey S, Comley LA, Blair A.

Am J Hum Genet. 1991 Jun;48(6):1214. No abstract available. PMID: 2035542 [PubMed - indexed for MEDLINE]Related articlesFree article

Prevalence of fragile X syndrome.

Webb T, Bundey S.

J Med Genet. 1991 May;28(5):358. No abstract available. PMID: 1865479 [PubMed - indexed for MEDLINE]Related articlesFree article

A family with three sisters with the 4p- syndrome, originally reported as suffering from the Smith-Lemli-Opitz syndrome.

Hill S, Creasy M, Bundey S.

J Ment Defic Res. 1991 Feb;35 ( Pt 1):76-80.PMID: 2038028 [PubMed - indexed for MEDLINE]Related articles

Why do UK-born Pakistani babies have high perinatal and neonatal mortality rates?

Bundey S, Alam H, Kaur A, Mir S, Lancashire R.

Paediatr Perinat Epidemiol. 1991 Jan;5(1):101-14.PMID: 2000330 [PubMed - indexed for MEDLINE]Related articles

Severe dwarfism with cataracts. A new osteo-chondrodysplasia.

Chapman S, Bundey S, Fletcher RF.

Br J Radiol. 1990 Dec;63(756):971-4. No abstract available. PMID: 2268769 [PubMed - indexed for MEDLINE]Related articles

Adrenoleucodystrophy: a molecular genetic study in five families.

Del Mastro RG, Bundey S, Kilpatrick MW.

J Med Genet. 1990 Nov;27(11):670-5.PMID: 2277380 [PubMed - indexed for MEDLINE]Related articlesFree article

Very early onset Huntington's disease: genetic mechanism and risk to siblings.

Clarke DJ, Bundey S.

Clin Genet. 1990 Sep;38(3):180-6. Review.PMID: 2146048 [PubMed - indexed for MEDLINE]Related articles