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 *

201 related articles for article (PubMed ID: 20724852)

  • 41. [Comments on the letter to the editor regarding "Phototherapeutic keratectomy in recurrences of granular corneal dystrophy after keratoplasty"].
    Kroll P
    Klin Monbl Augenheilkd; 1995 Nov; 207(5):343. PubMed ID: 8587311
    [No Abstract]   [Full Text] [Related]  

  • 42. 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. PubMed ID: 15531312
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Comment on: "Phototherapeutic keratectomy in recurrence of granular corneal dystrophy after keratoplasty"].
    Vogel M
    Klin Monbl Augenheilkd; 1995 Aug; 207(2):143. PubMed ID: 7474778
    [No Abstract]   [Full Text] [Related]  

  • 44. Different recurrence patterns after phototherapeutic keratectomy in the corneal dystrophy resulting from homozygous and heterozygous R124H BIG-H3 mutation.
    Inoue T; Watanabe H; Yamamoto S; Inoue Y; Okada M; Hori Y; Maeda N; Inoue Y; Hayashi K; Shimomura Y; Tano Y
    Am J Ophthalmol; 2001 Aug; 132(2):255-7. PubMed ID: 11476689
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Laser refractive surgery in corneal dystrophies.
    Rocha-de-Lossada C; Rachwani-Anil R; Colmenero-Reina E; Borroni D; Sánchez-González JM
    J Cataract Refract Surg; 2021 May; 47(5):662-670. PubMed ID: 33149045
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Classification of corneal dystrophies].
    Lisch W
    Klin Monbl Augenheilkd; 2006 Oct; 223(10):828. PubMed ID: 17063426
    [No Abstract]   [Full Text] [Related]  

  • 47. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
    Correa-Gomez V; Villalvazo-Cordero L; Zenteno JC
    Mol Vis; 2007 Sep; 13():1695-700. PubMed ID: 17893671
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
    Zhao XC; Nakamura H; Subramanyam S; Stock LE; Gillette TE; Yoshikawa S; Ma X; Yee RW
    Ophthalmology; 2007 Nov; 114(11):e39-46. PubMed ID: 17980739
    [TBL] [Abstract][Full Text] [Related]  

  • 49. The changes in corneal biomechanical parameters after phototherapeutic keratectomy in eyes with granular corneal dystrophy.
    Kamiya K; Shimizu K; Ohmoto F
    Eye (Lond); 2009 Sep; 23(9):1790-5. PubMed ID: 19098706
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A novel mutation of the TGFBI gene causing a lattice corneal dystrophy with deep stromal involvement.
    Kawasaki S; Yagi H; Yamasaki K; Matsuda A; Takeda K; Kinoshita S
    Br J Ophthalmol; 2011 Jan; 95(1):150-1. PubMed ID: 20974628
    [No Abstract]   [Full Text] [Related]  

  • 51. Treatment of lisch corneal dystrophy with photorefractive keratectomy and mitomycin C.
    Wessel MM; Sarkar JS; Jakobiec FA; Dang N; Bhat P; Michaud N; Starr CE
    Cornea; 2011 Apr; 30(4):481-5. PubMed ID: 21045666
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Deep anterior lamellar keratoplasty in Korean patients with Avellino dystrophy.
    Park KA; Ki CS; Chung ES; Chung TY
    Cornea; 2007 Oct; 26(9):1132-5. PubMed ID: 17893551
    [TBL] [Abstract][Full Text] [Related]  

  • 53. De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy.
    Hilton EN; Black GC; Manson FD; Schorderet DF; Munier FL
    Br J Ophthalmol; 2007 Aug; 91(8):1083-4. PubMed ID: 17638818
    [No Abstract]   [Full Text] [Related]  

  • 54. Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of Avellino corneal dystrophy.
    Lisch W; Moller HU
    Cornea; 2011 Aug; 30(8):949; author reply 949-50. PubMed ID: 21617530
    [No Abstract]   [Full Text] [Related]  

  • 55. Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L mutation of the BIGH3 gene.
    Dighiero P; Valleix S; D'Hermies F; Drunat S; Ellies P; Savoldelli M; Pouliquen Y; Delpech M; Legeais JM; Renard G
    Ophthalmology; 2000 Jul; 107(7):1353-7. PubMed ID: 10889112
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Post-LASIK exacerbation of granular corneal dystrophy type 2 in members of a chinese family.
    Chao-Shern C; Me R; DeDionisio LA; Ke BL; Nesbit MA; Marshall J; Moore CBT
    Eye (Lond); 2018 Jan; 32(1):39-43. PubMed ID: 29192679
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Novel TGFBI mutation p.(Leu558Arg) in a lattice corneal dystrophy patient.
    Dudakova L; Palos M; Jirsova K; Skalicka P; Dundr P; Liskova P
    Ophthalmic Genet; 2016 Dec; 37(4):473-474. PubMed ID: 27028151
    [No Abstract]   [Full Text] [Related]  

  • 58. [Early recurrence of Groenouw type I corneal dystrophy after phototherapeutic keratectomy. Molecular biology study suggests epithelial genesis].
    Chiambaretta F; Pilon F; Deriot JB; Gerard M; Couleangon ML; Schorderet DF; Kemeny JL; Dastugue B; Creveaux I; Rigal D
    J Fr Ophtalmol; 2004 May; 27(5):449-56. PubMed ID: 15179300
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Unusual phenotype of an individual with the R124C mutation in the TGFBI gene.
    Morishige N; Chikama T; Ishimura Y; Nishida T; Takahashi M; Mashima Y
    Arch Ophthalmol; 2004 Aug; 122(8):1224-7. PubMed ID: 15302666
    [No Abstract]   [Full Text] [Related]  

  • 60. Phototherapeutic keratectomy in the treatment of Avellino dystrophy.
    Cennamo G; Rosa N; Rosenwasser GO; Sebastiani A
    Ophthalmologica; 1994; 208(4):198-200. PubMed ID: 7970546
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.