Literature DB >> 13570776

Dominant hereditary optic atrophy with bitemporal field defects.

P T MANCHESTER, F P CALHOUN.   

Abstract

Entities:  

Keywords:  HEMIANOPIA; NERVES, OPTIC/diseases

Mesh：

Year:  1958        PMID： 13570776     DOI： 10.1001/archopht.1958.00940080497021

Source DB:  PubMed          Journal:  AMA Arch Ophthalmol        ISSN： 0096-6339


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  6 in total

Review 1.  LEBER'S DISEASE IN THE NETHERLANDS.

Authors:  A H VANSENUS
Journal:  Doc Ophthalmol       Date:  1963       Impact factor: 2.379

2.  [Hereditary optic atrophies].

Authors:  C M Poloschek; W A Lagrèze
Journal:  Ophthalmologe       Date:  2009-09       Impact factor: 1.059

Review 3.  Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

4.  Biotinidase Deficiency, Bilateral Optic Atrophy, and a Visual Field Defect.

Authors:  Sarah Chamney; Vasuki Gnana Jothi; Eibhlin McLoone
Journal:  Neuroophthalmology       Date:  2013-11-19

5.  Clinical approach to optic neuropathies.

Authors:  Raed Behbehani
Journal:  Clin Ophthalmol       Date:  2007-09

Review 6.  A review of primary hereditary optic neuropathies.

Authors:  M Votruba; S Aijaz; A T Moore
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982
  6 in total

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