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    Results: 1 to 20 of 322

    1.

    Aetiology of congenital and paediatric cataract in an Australian population.

    Wirth MG, Russell-Eggitt IM, Craig JE, Elder JE, Mackey DA.

    Br J Ophthalmol. 2002 Jul;86(7):782-6.PMID: 12084750 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Hereditary hyperferritinemia-cataract syndrome: prevalence, lens morphology, spectrum of mutations, and clinical presentations.

    Craig JE, Clark JB, McLeod JL, Kirkland MA, Grant G, Elder JE, Toohey MG, Kowal L, Savoia HF, Chen C, Roberts S, Wirth MG, Mackey DA.

    Arch Ophthalmol. 2003 Dec;121(12):1753-61.PMID: 14662596 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Autosomal dominant congenital cataract. Interocular phenotypic variability.

    Scott MH, Hejtmancik JF, Wozencraft LA, Reuter LM, Parks MM, Kaiser-Kupfer MI.

    Ophthalmology. 1994 May;101(5):866-71.PMID: 8190472 [PubMed - indexed for MEDLINE]Related articles

    4.

    Non-syndromic posterior lenticonus a cause of childhood cataract: evidence for X-linked inheritance.

    Russell-Eggitt IM.

    Eye (Lond). 2000 Dec;14(Pt 6):861-3.PMID: 11584843 [PubMed - indexed for MEDLINE]Related articles

    5.

    A missense mutation in LIM2 causes autosomal recessive congenital cataract.

    Ponnam SP, Ramesha K, Tejwani S, Matalia J, Kannabiran C.

    Mol Vis. 2008 Jun 23;14:1204-8.PMID: 18596884 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Juvenile cataract with autosomal recessive inheritance. A study from the Aland Islands, Finland.

    Forsius H, Arentz-Grastvedt B, Eriksson AW.

    Acta Ophthalmol (Copenh). 1992 Feb;70(1):26-32.PMID: 1557971 [PubMed - indexed for MEDLINE]Related articles

    7.

    Have we stopped looking for a red reflex in newborn screening?

    Sotomi O, Ryan CA, O'Connor G, Murphy BP.

    Ir Med J. 2007 Mar;100(3):398-400.PMID: 17491540 [PubMed - indexed for MEDLINE]Related articles

    8.

    Congenital cataract etiology.

    El Fkih L, Hmaied W, El Hif S, Moalla S, Marakchi S, Tabib N, Azzouz H.

    Tunis Med. 2007 Dec;85(12):1025-9.PMID: 19170381 [PubMed - indexed for MEDLINE]Related articles

    9.

    Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

    Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM.

    Br J Ophthalmol. 2004 Jan;88(1):79-83.PMID: 14693780 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    [Complicated cataracts in various forms of retinitis pigmentosa. Type and incidence]

    Auffarth GU, Tetz MR, Krastel H, Blankenagel A, Völcker HE.

    Ophthalmologe. 1997 Sep;94(9):642-6. Review. German. PMID: 9410231 [PubMed - indexed for MEDLINE]Related articles

    11.

    Visual outcome in patients with isolated autosomal dominant congenital cataract.

    Francis PJ, Ionides A, Berry V, Bhattacharya S, Moore AT.

    Ophthalmology. 2001 Jun;108(6):1104-8.PMID: 11382637 [PubMed - indexed for MEDLINE]Related articles

    12.

    Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations.

    Forshew T, Johnson CA, Khaliq S, Pasha S, Willis C, Abbasi R, Tee L, Smith U, Trembath RC, Mehdi SQ, Moore AT, Maher ER.

    Hum Genet. 2005 Sep;117(5):452-9. Epub 2005 Jun 16.PMID: 15959809 [PubMed - indexed for MEDLINE]Related articles

    13.

    Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract.

    Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS.

    Invest Ophthalmol Vis Sci. 2007 May;48(5):2208-13.PMID: 17460281 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13.

    Watts P, Rees M, Clarke A, Beck L, Lane C, Owen MJ, Gray J.

    Eye (Lond). 2000 Apr;14 ( Pt 2):172-5.PMID: 10845011 [PubMed - indexed for MEDLINE]Related articles

    15.

    Aetiology of childhood cataract in south India.

    Eckstein M, Vijayalakshmi P, Killedar M, Gilbert C, Foster A.

    Br J Ophthalmol. 1996 Jul;80(7):628-32.PMID: 8795375 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    A nationwide Danish study of 1027 cases of congenital/infantile cataracts: etiological and clinical classifications.

    Haargaard B, Wohlfahrt J, Fledelius HC, Rosenberg T, Melbye M.

    Ophthalmology. 2004 Dec;111(12):2292-8.PMID: 15582089 [PubMed - indexed for MEDLINE]Related articles

    17.

    A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from Pakistan.

    Sajjad N, Goebel I, Kakar N, Cheema AM, Kubisch C, Ahmad J.

    BMC Med Genet. 2008 Nov 11;9:99.PMID: 19014451 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Juvenile cataract in Hutterites.

    Shokeir MH, Lowry RB.

    Am J Med Genet. 1985 Nov;22(3):495-500.PMID: 4061486 [PubMed - indexed for MEDLINE]Related articles

    19.

    [Genetic examination in cases of congenital cataract]

    Lorenz B.

    Ophthalmologe. 2007 Jul;104(7):559-65. Review. German. PMID: 17571268 [PubMed - indexed for MEDLINE]Related articles

    20.

    Localization of autosomal recessive congenital cataracts in consanguineous Pakistani families to a new locus on chromosome 1p.

    Butt T, Yao W, Kaul H, Xiaodong J, Gradstein L, Zhang Y, Husnain T, Riazuddin S, Hejtmancik JF, Riazuddin SA.

    Mol Vis. 2007 Sep 10;13:1635-40.PMID: 17893665 [PubMed - indexed for MEDLINE]Related articlesFree article

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