Literature DB >> 5793652

Ocular findings in hereditary diaphyseal cysplasia (Engelmann's disease).

P H Morse, F B Walsh, J R McCormick.   

Abstract

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Year:  1969        PMID： 5793652     DOI： 10.1016/0002-9394(69)94939-3

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


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  4 in total

1.  Papilloedema, a complication of progressive diaphyseal dysplasia: a series of three case reports.

Authors:  M Wright; N R Miller; R M McFadzean; P Riordan-Eva; A G Lee; M D Sanders; G G McIlwaine
Journal:  Br J Ophthalmol       Date:  1998-09       Impact factor: 4.638

2.  Papilledema with Camurati-Engelmann disease instigating loss of ganglion cell complex thickness.

Authors:  Satoshi Okimoto; Junichi Kawahara; Yoshiaki Kiuchi
Journal:  Jpn J Ophthalmol       Date:  2011-02-18       Impact factor: 2.447

Review 3.  A method for volume determination of the orbit and its contents by high resolution axial tomography and quantitative digital image analysis.

Authors:  W C Cooper
Journal:  Trans Am Ophthalmol Soc       Date:  1985

Review 4.  Craniotubular bone disorders.

Authors:  R J Gorlin
Journal:  Pediatr Radiol       Date:  1994
  4 in total

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