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Journal Abstract Search

261 related items for PubMed ID: 25291437

  • 1. Anterior segment developmental anomalies in a 33-week-old fetus with MIDAS syndrome.
    Herwig MC, Loeffler KU, Gembruch U, Kuchelmeister K, Müller AM.
    Pediatr Dev Pathol; 2014; 17(6):491-5. PubMed ID: 25291437
    [Abstract] [Full Text] [Related]

  • 2. Loss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly.
    Zhao J, Kawai K, Wang H, Wu D, Wang M, Yue Z, Zhang J, Liu YH.
    Am J Pathol; 2012 Jun; 180(6):2230-9. PubMed ID: 22503753
    [Abstract] [Full Text] [Related]

  • 3. Microphthalmia with linear skin defects syndrome.
    García-Rabasco A, De-Unamuno B, Martínez F, Febrer-Bosch I, Alegre-de-Miquel V.
    Pediatr Dermatol; 2013 Jun; 30(6):e230-1. PubMed ID: 22612277
    [Abstract] [Full Text] [Related]

  • 4. MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome.
    Happle R, Daniëls O, Koopman RJ.
    Am J Med Genet; 1993 Oct 01; 47(5):710-3. PubMed ID: 8267001
    [Abstract] [Full Text] [Related]

  • 5. A case of atypical WAGR syndrome with anterior segment anomaly and microphthalmos.
    Kawase E, Tanaka K, Honna T, Azuma N.
    Arch Ophthalmol; 2001 Dec 01; 119(12):1855-6. PubMed ID: 11735802
    [No Abstract] [Full Text] [Related]

  • 6. Congenital anterior staphyloma associated with Peters' anomaly and aphakia in a Holstein calf.
    Sato R, Onda K, Murakami M, Ito D, Madarame H.
    J Vet Med Sci; 2017 Jul 07; 79(7):1151-1154. PubMed ID: 28529272
    [Abstract] [Full Text] [Related]

  • 7. Septo-optic dysplasia associated with bilateral complex microphthalmos.
    Gündüz K, Günalp I, Saatçi I.
    Ophthalmic Genet; 1996 Sep 07; 17(3):109-13. PubMed ID: 8905851
    [Abstract] [Full Text] [Related]

  • 8. A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphyloma.
    Tarlan B, Kiratli H, Kılıç E, Utine E, Boduroğlu K.
    Ophthalmic Genet; 2014 Dec 07; 35(4):248-51. PubMed ID: 23834556
    [Abstract] [Full Text] [Related]

  • 9. Peters anomaly in cri-du-chat syndrome.
    Hope WC, Cordovez JA, Capasso JE, Hammersmith KM, Eagle RC, Lall-Trail J, Levin AV.
    J AAPOS; 2015 Jun 07; 19(3):277-9. PubMed ID: 26059676
    [Abstract] [Full Text] [Related]

  • 10. Bilateral anterior segment dysgenesis with the presumed Peters' anomaly in a cat.
    Park S, Kim K, Kim Y, Seo K.
    J Vet Med Sci; 2018 Feb 20; 80(2):297-301. PubMed ID: 29249729
    [Abstract] [Full Text] [Related]

  • 11. 8q21.11 microdeletion in two patients with syndromic peters anomaly.
    Happ H, Schilter KF, Weh E, Reis LM, Semina EV.
    Am J Med Genet A; 2016 Sep 20; 170(9):2471-5. PubMed ID: 27378168
    [Abstract] [Full Text] [Related]

  • 12. Clinical outcome of penetrating keratoplasty in patients 5 years or younger: peters anomaly versus sclerocornea.
    Kim YW, Choi HJ, Kim MK, Wee WR, Yu YS, Oh JY.
    Cornea; 2013 Nov 20; 32(11):1432-6. PubMed ID: 24104853
    [Abstract] [Full Text] [Related]

  • 13. [COX7B mutations in MIDAS syndrome or microphthalmia with linear skin defects (MLS)].
    Dereure O.
    Ann Dermatol Venereol; 2013 May 20; 140(5):405-6. PubMed ID: 23663720
    [No Abstract] [Full Text] [Related]

  • 14. [Mesodermal dysgenesis of the anterior segment].
    Damian C.
    Oftalmologia; 1992 May 20; 36(4):391-5. PubMed ID: 1420131
    [Abstract] [Full Text] [Related]

  • 15. A rare case of type 1 unilateral 'peripheral' Peters' anomaly.
    Shah C, Sen P, Mohan A, Chandra K, Jain E.
    Indian J Ophthalmol; 2019 Oct 20; 67(10):1702-1703. PubMed ID: 31546519
    [No Abstract] [Full Text] [Related]

  • 16. Clinical features of anterior segment dysgenesis associated with congenital corneal opacities.
    Shigeyasu C, Yamada M, Mizuno Y, Yokoi T, Nishina S, Azuma N.
    Cornea; 2012 Mar 20; 31(3):293-8. PubMed ID: 22157569
    [Abstract] [Full Text] [Related]

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  • 19. Unilateral Peters' anomaly complicated by a corneal tattoo.
    Pomella KM, Wagner H.
    Optom Vis Sci; 1998 Sep 20; 75(9):635-9. PubMed ID: 9778695
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