These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 7315222)

  • 21. A Korean family with an early-onset autosomal dominant macular dystrophy resembling North Carolina macular dystrophy.
    Kim SJ; Woo SJ; Yu HG
    Korean J Ophthalmol; 2006 Dec; 20(4):220-4. PubMed ID: 17302207
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Autosomal dominant macular dystrophy simulating North Carolina macular dystrophy.
    Holz FG; Evans K; Gregory CY; Bhattacharya S; Bird AC
    Arch Ophthalmol; 1995 Feb; 113(2):178-84. PubMed ID: 7864750
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A North Carolina macular dystrophy phenotype in a Belizean family maps to the MCDR1 locus.
    Rabb MF; Mullen L; Yelchits S; Udar N; Small KW
    Am J Ophthalmol; 1998 Apr; 125(4):502-8. PubMed ID: 9559736
    [TBL] [Abstract][Full Text] [Related]  

  • 24. An early-onset autosomal dominant macular dystrophy (MCDR3) resembling North Carolina macular dystrophy maps to chromosome 5.
    Michaelides M; Johnson S; Tekriwal AK; Holder GE; Bellmann C; Kinning E; Woodruff G; Trembath RC; Hunt DM; Moore AT
    Invest Ophthalmol Vis Sci; 2003 May; 44(5):2178-83. PubMed ID: 12714659
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Long-term follow-up of dominant macular dystrophy with flecks (Stargardt).
    Mansour AM
    Ophthalmologica; 1992; 205(3):138-43. PubMed ID: 1475092
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Central areolar pigment epithelial dystrophy.
    Fetkenhour CL; Gurney N; Dobbie JG; Choromokos E
    Am J Ophthalmol; 1976 Jun; 81(6):745-53. PubMed ID: 937428
    [TBL] [Abstract][Full Text] [Related]  

  • 27. An autosomal dominant bull's-eye macular dystrophy (MCDR2) that maps to the short arm of chromosome 4.
    Michaelides M; Johnson S; Poulson A; Bradshaw K; Bellmann C; Hunt DM; Moore AT
    Invest Ophthalmol Vis Sci; 2003 Apr; 44(4):1657-62. PubMed ID: 12657606
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Atrophic maculopathy associated with hereditary ataxia.
    Duinkerke-Eerola KU; Cruysberg JR; Deutman AF
    Am J Ophthalmol; 1980 Nov; 90(5):597-603. PubMed ID: 7446640
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Autosomal dominant hemorrhagic macular dystrophy not associated with the TIMP3 gene.
    Ayyagari R; Griesinger IB; Bingham E; Lark KK; Moroi SE; Sieving PA
    Arch Ophthalmol; 2000 Jan; 118(1):85-92. PubMed ID: 10636420
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [North Carolina macular dystrophy. Hereditary macular disease with good functional prognosis].
    Schworm HD; Ulbig MW; Hoops J; Rudolph G; Weber BH; Ehrt O; Boergen KP
    Ophthalmologe; 1998 Jan; 95(1):13-8. PubMed ID: 9531796
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Various fundus manifestations in a Japanese family with Best's vitelliform macular dystrophy.
    Shibuya Y; Hayasaka S
    Jpn J Ophthalmol; 1993; 37(4):478-84. PubMed ID: 8145393
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The variable expressivity of a family with central areolar pigment epithelial dystrophy.
    Keithahn MA; Huang M; Keltner JL; Small KW; Morse LS
    Ophthalmology; 1996 Mar; 103(3):406-15. PubMed ID: 8600416
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Best's vitelliform dystrophy.
    Blodi CF; Stone EM
    Ophthalmic Paediatr Genet; 1990 Mar; 11(1):49-59. PubMed ID: 2190134
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Sporadic butterfly macular dystrophy.
    Mejia JR; Gieser RG
    Ann Ophthalmol; 1981 Nov; 13(11):1253-4. PubMed ID: 7325502
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Autosomal dominant Stargardt-like macular dystrophy: identification of a new family with a mutation in the ELOVL4 gene.
    Vrabec TR; Tantri A; Edwards A; Frost A; Donoso LA
    Am J Ophthalmol; 2003 Sep; 136(3):542-5. PubMed ID: 12967813
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Hereditary macular dystrophy without visible fundus abnormality.
    Miyake Y; Ichikawa K; Shiose Y; Kawase Y
    Am J Ophthalmol; 1989 Sep; 108(3):292-9. PubMed ID: 2774037
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical and genetic evidence for autosomal dominant North Carolina macular dystrophy in a German family.
    Pauleikhoff D; Sauer CG; Müller CR; Radermacher M; Merz A; Weber BH
    Am J Ophthalmol; 1997 Sep; 124(3):412-5. PubMed ID: 9439376
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.
    Stone EM; Nichols BE; Kimura AE; Weingeist TA; Drack A; Sheffield VC
    Arch Ophthalmol; 1994 Jun; 112(6):765-72. PubMed ID: 8002834
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Butterfly-shaped macular dystrophy in four generations.
    Prensky JG; Bresnick GH
    Arch Ophthalmol; 1983 Aug; 101(8):1198-203. PubMed ID: 6882245
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Unusual associations of pattern dystrophies].
    Lodato G; Giuffré G
    J Fr Ophtalmol; 1985; 8(2):147-54. PubMed ID: 4008873
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.