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.
378 related articles for article (PubMed ID: 9379642)
1. [Schnyder corneal dystrophy and juvenile, systemic hypercholesteremia]. Kohnen T; Pelton RW; Jones DB Klin Monbl Augenheilkd; 1997 Aug; 211(2):135-7. PubMed ID: 9379642 [TBL] [Abstract][Full Text] [Related]
2. Central corneal mosaic opacities in Schnyder's crystalline dystrophy. Wu CW; Lin PY; Liu YF; Liu TC; Lin MW; Chen WM; Lee FL; Lee SM; Hsu WM Ophthalmology; 2005 Apr; 112(4):650-3. PubMed ID: 15808257 [TBL] [Abstract][Full Text] [Related]
3. [Schnyder's crystalline dystrophy. II. Association with genu valgum]. Hoang-Xuan T; Pouliquen Y; Gasteau J J Fr Ophtalmol; 1985; 8(11):743-7. PubMed ID: 3879611 [TBL] [Abstract][Full Text] [Related]
6. Schnyder's dystrophy of the cornea. A Swede-Finn connection. Weiss JS Cornea; 1992 Mar; 11(2):93-101. PubMed ID: 1582223 [TBL] [Abstract][Full Text] [Related]
7. Ultrastructural changes in the posterior layers of the cornea in Schnyder's crystalline dystrophy. Freddo TF; Polack FM; Leibowitz HM Cornea; 1989 Sep; 8(3):170-7. PubMed ID: 2663345 [TBL] [Abstract][Full Text] [Related]
8. [Schnyder's crystalline dystrophy. I. Study of a case by light and electron microscopy]. Hoang-Xuan T; Pouliquen Y; Savoldelli M; Gasteau J J Fr Ophtalmol; 1985; 8(11):735-42. PubMed ID: 3914502 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. In vivo confocal microscopy of a family with Schnyder crystalline corneal dystrophy. Vesaluoma MH; Linna TU; Sankila EM; Weiss JS; Tervo TM Ophthalmology; 1999 May; 106(5):944-51. PubMed ID: 10328394 [TBL] [Abstract][Full Text] [Related]
12. [Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36?]. Riebeling P; Polz S; Tost F; Weiss JS; Kuivaniemi H; Hoeltzenbein M Ophthalmologe; 2003 Nov; 100(11):979-83. PubMed ID: 14669035 [TBL] [Abstract][Full Text] [Related]
17. Morphological evaluation of Schnyder's central crystalline dystrophy by confocal microscopy before and after phototherapeutic keratectomy. Ciancaglini M; Carpineto P; Doronzo E; Nubile M; Zuppardi E; Mastropasqua L J Cataract Refract Surg; 2001 Nov; 27(11):1892-5. PubMed ID: 11709268 [TBL] [Abstract][Full Text] [Related]
18. Posterior amorphous corneal dystrophy. An ultrastructural study of a variant with histopathological features of an endothelial dystrophy. Roth SI; Mittelman D; Stock EL Cornea; 1992 Mar; 11(2):165-72. PubMed ID: 1582220 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark. Jensen HK Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]