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 *

175 related articles for article (PubMed ID: 14767659)

  • 1. A case of corneal dystrophy treated with automated lamellar therapeutic keratoplasty.
    Sato H; Fukuda M; Hibino T; Shimomura Y; Yamamoto S
    Jpn J Ophthalmol; 2004; 48(1):79-81. PubMed ID: 14767659
    [No Abstract]   [Full Text] [Related]  

  • 2. Clinical and immunopathological corneal phenotype in homozygotes for the BIGH3 R124H mutation.
    Diaper CJ; Schorderet DF; Chaubert P; Munier FL
    Eye (Lond); 2005 Jan; 19(1):92-6. PubMed ID: 15094731
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygous granular corneal dystrophy type II (Avellino corneal dystrophy): natural history and progression after treatment.
    Moon JW; Kim SW; Kim TI; Cristol SM; Chung ES; Kim EK
    Cornea; 2007 Oct; 26(9):1095-100. PubMed ID: 17893542
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical findings and treatments of granular corneal dystrophy type 2 (avellino corneal dystrophy): a review of the literature.
    Han KE; Kim TI; Chung WS; Choi SI; Kim BY; Kim EK
    Eye Contact Lens; 2010 Sep; 36(5):296-9. PubMed ID: 20724852
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 17317389
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. In vivo laser confocal microscopy findings for Bowman's layer dystrophies (Thiel-Behnke and Reis-Bücklers corneal dystrophies).
    Kobayashi A; Sugiyama K
    Ophthalmology; 2007 Jan; 114(1):69-75. PubMed ID: 17198850
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.
    Takács L; Losonczy G; Matesz K; Balogh I; Sohajda Z; Tóth K; Fazakas F; Vereb G; Berta A
    Mol Vis; 2007 Oct; 13():1976-83. PubMed ID: 17982422
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recurrent granular dystrophy of the cornea: an unusual case.
    Frising M; Wildhardt G; Frisch L; Pitz S
    Cornea; 2006 Jun; 25(5):614-7. PubMed ID: 16783153
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 15885785
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Comparative evaluation of big-bubble deep anterior lamellar keratoplasty and penetrating keratoplasty in a case of macular corneal dystrophy.
    Patel AK; Nayak H; Kumar V
    Cornea; 2009 Jun; 28(5):583-5. PubMed ID: 19421034
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of human transforming growth factor beta-induced gene mutation in corneal dystrophy.
    Li Y; Sun XG; Ren HY; Dong B; Wang ZQ; Sun XY
    Chin Med J (Engl); 2004 Sep; 117(9):1418-21. PubMed ID: 15377440
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Atypical Corneal Deposits after Deep Anterior Lamellar Keratoplasty.
    Bonnet C; Aldave AJ
    Ophthalmology; 2020 Apr; 127(4):466. PubMed ID: 32200838
    [No Abstract]   [Full Text] [Related]  

  • 16. Comparison of deep lamellar keratoplasty and penetrating keratoplasty for lattice and macular corneal dystrophies.
    Kawashima M; Kawakita T; Den S; Shimmura S; Tsubota K; Shimazaki J
    Am J Ophthalmol; 2006 Aug; 142(2):304-9. PubMed ID: 16876513
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Lattice corneal dystrophy type III in patients with a homozygous L527R mutation in the TGFBI gene.
    Funayama T; Mashima Y; Kawashima M; Yamada M
    Jpn J Ophthalmol; 2006; 50(1):62-4. PubMed ID: 16453189
    [No Abstract]   [Full Text] [Related]  

  • 19. Lattice corneal dystrophy type I without typical lattice lines: role of mutational analysis.
    Yoshida S; Yoshida A; Nakao S; Emori A; Nakamura T; Fujisawa K; Kumano Y; Ishibashi T
    Am J Ophthalmol; 2004 Mar; 137(3):586-8. PubMed ID: 15013897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
    Tian X; Fujiki K; Zhang Y; Murakami A; Li Q; Kanai A; Wang W; Hao Y; Ma Z
    Am J Ophthalmol; 2007 Sep; 144(3):473-5. PubMed ID: 17765440
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.