Literature DB >> 15459793

[Central pigment epithelial defect in a 33 year-old female patient. A 33 year-old female patient with neurological symptoms, central pigment epithelial defect and limited upward gaze].

A H Wolf1, C Gass, A Kampik, G Rudolph.   

Abstract

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Year:  2004        PMID： 15459793     DOI： 10.1007/s00347-003-0921-0

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN： 0941-293X            Impact factor:   1.059


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  6 in total

Review 1.  Mitochondrial DNA mutations in human disease.

Authors:  S DiMauro; E A Schon
Journal:  Am J Med Genet       Date:  2001

2.  [Ocular changes in MELAS syndrome].

Authors:  M Küchle; P M Brenner; A Engelhardt; G O Naumann
Journal:  Klin Monbl Augenheilkd       Date:  1990-09       Impact factor: 0.700

Review 3.  [Eye diseases in mitochondrial encephalomyopathies].

Authors:  D Mojon
Journal:  Ther Umsch       Date:  2001-01

4.  Fundus changes in patients with the mitochondrial DNA point mutation at position 3243.

Authors:  C Bonte; A Leys; G Matthijs; L Missotten
Journal:  Bull Soc Belge Ophtalmol       Date:  1996

5.  Ocular clinicopathologic study of the mitochondrial encephalomyopathy overlap syndromes.

Authors:  T S Chang; D R Johns; D Walker; Z de la Cruz; I H Maumence; W R Green
Journal:  Arch Ophthalmol       Date:  1993-09

6.  Ocular pathology of MELAS syndrome with mitochondrial DNA nucleotide 3243 point mutation.

Authors:  V Rummelt; R Folberg; V Ionasescu; H Yi; K C Moore
Journal:  Ophthalmology       Date:  1993-12       Impact factor: 12.079
  6 in total
  1 in total

1.  [Classification of biomedical research reports as a reference for evidence-based medicine in ophthalmology. A survey considering as example the journal Der Ophthalmologe].

Authors:  H P N Scholl; M Fleckenstein; T U Krohne; F G Holz
Journal:  Ophthalmologe       Date:  2005-12       Impact factor: 1.059
  1 in total

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