Literature DB >> 21331705

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

Satoshi Okimoto, Junichi Kawahara, Yoshiaki Kiuchi.   

Abstract

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Year:  2011        PMID: 21331705     DOI: 10.1007/s10384-010-0905-y

Source DB:  PubMed          Journal:  Jpn J Ophthalmol        ISSN: 0021-5155            Impact factor:   2.447


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  6 in total

1.  MR of multiple cranial neuropathies in a patient with camurati-engelmann disease: case report.

Authors:  L J Applegate; G R Applegate; S S Kemp
Journal:  AJNR Am J Neuroradiol       Date:  1991 May-Jun       Impact factor: 3.825

2.  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

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

Authors:  P H Morse; F B Walsh; J R McCormick
Journal:  Am J Ophthalmol       Date:  1969-07       Impact factor: 5.258

4.  Pathogenesis of optic disc swelling.

Authors: 
Journal:  Br J Ophthalmol       Date:  1978-09       Impact factor: 4.638

5.  Glaucomatouslike visual field defects in chronic papilledema.

Authors:  F Grehn; S Knorr-Held; G Kommerell
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1981

6.  Progressive diaphyseal dysplasia: genetics and clinical and radiologic manifestations.

Authors:  Y Naveh; J K Kaftori; U Alon; J Ben-David; M Berant
Journal:  Pediatrics       Date:  1984-09       Impact factor: 7.124

  6 in total

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