Literature DB >> 4187513

Hereditary deep dystrophy of the cornea (polymorphous).

M J Hogan, G Bietti.   

Abstract

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Year:  1969        PMID: 4187513     DOI: 10.1016/0002-9394(69)94569-3

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


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  8 in total

1.  Posterior polymorphous dystrophy: a light and electron microscopic study.

Authors:  B L Johnson; S I Brown
Journal:  Br J Ophthalmol       Date:  1978-02       Impact factor: 4.638

2.  Posterior polymorphous keratopathy.

Authors:  G M Liakos; T A Casey
Journal:  Br J Ophthalmol       Date:  1978-01       Impact factor: 4.638

3.  In vivo confocal microscopic observations of eyes diagnosed with posterior corneal vesicles.

Authors:  Atsushi Shiraishi; Xiaodong Zheng; Yuri Sakane; Yuko Hara; Yasuhito Hayashi
Journal:  Jpn J Ophthalmol       Date:  2016-09-01       Impact factor: 2.447

4.  The nature of hereditary deep polymorphous dystrophy of the cornea: its association with iris and anterior chamber dygenesis.

Authors:  M Grayson
Journal:  Trans Am Ophthalmol Soc       Date:  1974

5.  [Histopathology of Schlichting's posterior polymorphous corneal dystrophy. I. Light microscopy findings in relation to clinical aspects].

Authors:  H Hanselmayer
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1972

6.  Posterior polymorphous dystrophy of the cornea (Schlichting). An unusual clinical variant.

Authors:  H Witschel; R Sundmacher; H Theopold; W Jaeger
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1980

7.  Posterior polymorphous corneal dystrophy: a disease characterized by epithelial-like endothelial cells which influence management and prognosis.

Authors:  J H Krachmer
Journal:  Trans Am Ophthalmol Soc       Date:  1985

8.  Combined macular dystrophy and cornea guttata: an electron microscopic study.

Authors:  Y Pouliquen; P Dhermy; G Renard; J P Giraud; M Savoldelli
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1980
  8 in total

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