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    Results: 25

    1.

    Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.

    Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel E, Papp J.

    Cornea. 2009 Aug;28(7):801-7.PMID: 19574904 [PubMed - indexed for MEDLINE]Related articles

    2.

    A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.

    Aldave AJ, Yellore VS, Sonmez B, Bourla N, Salem AK, Khan MA, Rayner SA, Glasgow BJ.

    Arch Ophthalmol. 2008 Mar;126(3):371-7.PMID: 18332318 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    A late-onset unilateral variant of lattice corneal dystrophy not associated with a TGFBI mutation.

    Yellore VS, Sonmez B, Rayner SA, Aldave AJ.

    Br J Ophthalmol. 2008 Mar;92(3):426-7. No abstract available. PMID: 18303168 [PubMed - indexed for MEDLINE]Related articles

    4.

    Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.

    Yellore VS, Khan MA, Bourla N, Rayner SA, Chen MC, Sonmez B, Momi RS, Sampat KM, Gorin MB, Aldave AJ.

    Mol Vis. 2007 Sep 24;13:1777-82.PMID: 17960116 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Posterior polymorphous corneal dystrophy is associated with TCF8 gene mutations and abdominal hernia.

    Aldave AJ, Yellore VS, Yu F, Bourla N, Sonmez B, Salem AK, Rayner SA, Sampat KM, Krafchak CM, Richards JE.

    Am J Med Genet A. 2007 Nov 1;143A(21):2549-56.PMID: 17935237 [PubMed - indexed for MEDLINE]Related articles

    6.

    An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation.

    Yellore VS, Sonmez B, Chen MC, Rayner SA, Thonar EJ, Aldave AJ.

    Ophthalmic Genet. 2007 Sep;28(3):169-74.PMID: 17896316 [PubMed - indexed for MEDLINE]Related articles

    7.

    Keratoconus is not associated with mutations in COL8A1 and COL8A2.

    Aldave AJ, Bourla N, Yellore VS, Rayner SA, Khan MA, Salem AK, Sonmez B.

    Cornea. 2007 Sep;26(8):963-5.PMID: 17721297 [PubMed - indexed for MEDLINE]Related articles

    8.

    Autosomal recessive CHED associated with novel compound heterozygous mutations in SLC4A11.

    Aldave AJ, Yellore VS, Bourla N, Momi RS, Khan MA, Salem AK, Rayner SA, Glasgow BJ, Kurtz I.

    Cornea. 2007 Aug;26(7):896-900.PMID: 17667634 [PubMed - indexed for MEDLINE]Related articles

    9.

    Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2.

    Aldave AJ, Sonmez B, Bourla N, Schultz G, Papp JC, Salem AK, Rayner SA, Yellore VS.

    Ophthalmic Genet. 2007 Jun;28(2):57-67.PMID: 17558846 [PubMed - indexed for MEDLINE]Related articles

    10.

    Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20.

    Yellore VS, Papp JC, Sobel E, Khan MA, Rayner SA, Farber DB, Aldave AJ.

    Genet Med. 2007 Apr;9(4):228-34.PMID: 17438387 [PubMed - indexed for MEDLINE]Related articles

    11.

    A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy.

    Aldave AJ, Sonmez B, Forstot SL, Rayner SA, Yellore VS, Glasgow BJ.

    Am J Ophthalmol. 2007 Mar;143(3):416-9. Epub 2006 Dec 29.PMID: 17317389 [PubMed - indexed for MEDLINE]Related articles

    12.

    No pathogenic mutations identified in the COL8A1 and COL8A2 genes in familial Fuchs corneal dystrophy.

    Aldave AJ, Rayner SA, Salem AK, Yoo GL, Kim BT, Saeedian M, Sonmez B, Yellore VS.

    Invest Ophthalmol Vis Sci. 2006 Sep;47(9):3787-90.PMID: 16936088 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    No VSX1 gene mutations associated with keratoconus.

    Aldave AJ, Yellore VS, Salem AK, Yoo GL, Rayner SA, Yang H, Tang GY, Piconell Y, Rabinowitz YS.

    Invest Ophthalmol Vis Sci. 2006 Jul;47(7):2820-2.PMID: 16799019 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    No pathogenic mutations identified in the TGFBI gene in polymorphic corneal amyloid deposition.

    Aldave AJ, Rayner SA, King JA, Salem AK, Prechanond A, Hashida S, Affeldt JC, Meallet MA, Glasgow BJ, Small KW, Yellore VS.

    Cornea. 2006 May;25(4):413-5.PMID: 16670477 [PubMed - indexed for MEDLINE]Related articles

    15.

    Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene.

    Aldave AJ, Rayner SA, Kim BT, Prechanond A, Yellore VS.

    Mol Vis. 2006 Feb 27;12:142-6.PMID: 16541014 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy.

    Aldave AJ, Rayner SA, Principe AH, Affeldt JA, Katsev D, Yellore VS.

    Mol Vis. 2005 Sep 2;11:713-6.PMID: 16163269 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene.

    Aldave AJ, Rayner SA, King JA, Affeldt JA, Yellore VS.

    Ophthalmology. 2005 Jun;112(6):1017-22.PMID: 15885785 [PubMed - indexed for MEDLINE]Related articles

    18.

    No pathogenic mutations identified in the COL8A2 gene or four positional candidate genes in patients with posterior polymorphous corneal dystrophy.

    Yellore VS, Rayner SA, Emmert-Buck L, Tabin GC, Raber I, Hannush SB, Stulting RD, Sampat K, Momi R, Principe AH, Aldave AJ.

    Invest Ophthalmol Vis Sci. 2005 May;46(5):1599-603.PMID: 15851557 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Candidate gene screening for posterior polymorphous dystrophy.

    Aldave AJ, Yellore VS, Principe AH, Abedi G, Merrill K, Chalukya M, Small KW, Udar N.

    Cornea. 2005 Mar;24(2):151-5.PMID: 15725882 [PubMed - indexed for MEDLINE]Related articles

    20.

    Lattice dystrophy-like localized amyloidosis of the cornea secondary to trichiasis.

    Aldave AJ, Principe AH, Lin DY, Yellore VS, Small KW.

    Cornea. 2005 Jan;24(1):112-5.PMID: 15604878 [PubMed - indexed for MEDLINE]Related articles

    21.

    Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.

    Aldave AJ, Gutmark JG, Yellore VS, Affeldt JA, Meallet MA, Udar N, Rao NA, Small KW, Klintworth GK.

    Am J Ophthalmol. 2004 Nov;138(5):772-81.PMID: 15531312 [PubMed - indexed for MEDLINE]Related articles

    22.

    The usefulness of buccal swabs for mutation screening in patients with suspected corneal dystrophies.

    Aldave AJ, Yellore VS, Self CA, Holsclaw D, Small K.

    Ophthalmology. 2004 Jul;111(7):1407-9.PMID: 15234146 [PubMed - indexed for MEDLINE]Related articles

    23.

    Anterior basement membrane corneal dystrophy and pseudo-unilateral lattice corneal dystrophy in a patient with recurrent corneal erosions.

    Aldave AJ, Lin DY, Principe AH, Yellore VS, Weissman BA.

    Am J Ophthalmol. 2004 Jun;137(6):1124-7.PMID: 15183802 [PubMed - indexed for MEDLINE]Related articles

    24.

    Novel mutations in the carbohydrate sulfotransferase gene (CHST6) in American patients with macular corneal dystrophy.

    Aldave AJ, Yellore VS, Thonar EJ, Udar N, Warren JF, Yoon MK, Cohen EJ, Rapuano CJ, Laibson PR, Margolis TP, Small K.

    Am J Ophthalmol. 2004 Mar;137(3):465-73.PMID: 15013869 [PubMed - indexed for MEDLINE]Related articles

    25.

    Atypical vortex pattern of corneal deposits in granular corneal dystrophy.

    Aldave AJ, Yellore VS, Hwang DG.

    Cornea. 2003 Nov;22(8):754-9.PMID: 14576527 [PubMed - indexed for MEDLINE]Related articles

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