Literature DB >> 1203237

Disc oedema in congenital amaurosis of Leber.

J T Flynn, R F Cullen.   

Abstract

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Year:  1975        PMID： 1203237      PMCID： PMC1042662          DOI： 10.1136/bjo.59.9.497

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


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  13 in total

1.  ELECTRON MICROSCOPY OF A RETINAL ABIOTROPHY.

Authors:  A J KROLL; T KUWABARA
Journal:  Arch Ophthalmol       Date:  1964-05

2.  [Histological findings in Leber's infantile amaurosis and in different forms of hemeralopia].

Authors:  J BABEL
Journal:  Ophthalmologica       Date:  1963       Impact factor: 3.250

3.  Development of the ERG in relation to histological differentiation of the retina in man and animals.

Authors:  G P HORSTEN; J E WINKELMAN
Journal:  Arch Ophthalmol       Date:  1960-02

4.  Retinal Aplasia as a Clinical Entity.

Authors:  A Sorsby; C E Williams
Journal:  Br Med J       Date:  1960-01-30

5.  [Histological findings in case of congenital pigmentary retinal degeneration].

Authors:  F VRABEC
Journal:  Ophthalmologica       Date:  1951-08       Impact factor: 3.250

6.  Congenital amaurosis of Leber.

Authors:  F D Gillespie
Journal:  Am J Ophthalmol       Date:  1966-05       Impact factor: 5.258

7.  Fluorescence angiography in circulatory disturbances in drusen of the optic disk.

Authors:  I Karel; J Otradovec; M Peleska
Journal:  Ophthalmologica       Date:  1972       Impact factor: 3.250

8.  Papilledema, optic neuritis, and pseudopapilledema. The use of fluorescein angiography in differential diagnosis.

Authors:  F B Walsh; C J Blair
Journal:  Trans Am Acad Ophthalmol Otolaryngol       Date:  1969 Sep-Oct

9.  Keratoconus in congenital diffuse tapetoretinal degeneration.

Authors:  I Karel
Journal:  Ophthalmologica       Date:  1968       Impact factor: 3.250

10.  Congenital amaurosis of retinal origin. Frequent association with neurological disorders.

Authors:  A Dekaban; R Carr
Journal:  Arch Neurol       Date:  1966-03
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  6 in total

1.  Histopathology and functional correlations in a patient with a mutation in RPE65, the gene for retinol isomerase.

Authors:  Vera L Bonilha; Mary E Rayborn; Yong Li; Gregory H Grossman; Eliot L Berson; Joe G Hollyfield
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-10-28       Impact factor: 4.799

2.  Leber's congenital amaurosis--a new syndrome with a cardiomyopathy.

Authors:  I M Russell-Eggitt; D S Taylor; P T Clayton; A Garner; A Kriss; J F Taylor
Journal:  Br J Ophthalmol       Date:  1989-04       Impact factor: 4.638

3.  Senior-Løken syndrome with marbelized fundus and unusual skeletal abnormalities. A case report.

Authors:  B Lauweryns; A Leys; E Van Haesendonck; L Missotten
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-04       Impact factor: 3.117

4.  A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.

Authors:  A T Moore; D S Taylor
Journal:  Br J Ophthalmol       Date:  1984-06       Impact factor: 4.638

5.  Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition.

Authors:  I K Jalili
Journal:  J Med Genet       Date:  1989-08       Impact factor: 6.318

6.  Yellowish flecks in Leber's congenital amaurosis.

Authors:  E Chew; A Deutman; A Pinckers; A Aan de Kerk
Journal:  Br J Ophthalmol       Date:  1984-10       Impact factor: 4.638
  6 in total

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