Wagner vitreoretinal degeneration. Follow-up of the original pedigree. (Q54739483)

3 June 2018

title

Wagner vitreoretinal degeneration. Follow-up of the original pedigree. (English)

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3 June 2018

author name string

Graemiger RA

1

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3 June 2018

Niemeyer G

2

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3 June 2018

Schneeberger SA

3

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3 June 2018

Messmer EP

4

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3 June 2018

publication date

1 December 1995

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3 June 2018

published in

Ophthalmology

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3 June 2018

volume

102

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3 June 2018

issue

12

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3 June 2018

page(s)

1830-1839

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3 June 2018

[On the clinical manifestation and pathology of degeneratio hyaloideoretinalis hereditaria (Wagner)]

cites work

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7 January 2021

Degeneratio Hyaloideo-Retinalis Hereditaria

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7 January 2021

Vitreoretinal Degeneration as a Sign of Generalized Connective Tissue Diseases

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7 January 2021

Erosive Vitreoretinopathy

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7 January 2021

The Stickler syndrome: evidence for close linkage to the structural gene for type II collagen

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7 January 2021

Stop codon in the procollagen II gene (COL2A1) in a family with the Stickler syndrome (arthro-ophthalmopathy)

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https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930787-7

7 January 2021

Procollagen II Gene Mutation in Stickler Syndrome

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https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930787-7

7 January 2021

Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14

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https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930787-7

7 January 2021

Rod Responses in Retinitis Pigmentosa, Dominantly Inherited

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7 January 2021

ERG in Behçet's disease (author's transl)

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7 January 2021

[Increase in the amplitude of the b-wave of the cone electroretinogram during light adaptation]

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7 January 2021

Wagner's Hereditary Vitreoretinal Degeneration and Retinal Detachment

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https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930787-7

7 January 2021

Wagner's hereditary vitreoretinal degeneration.

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https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930787-7

7 January 2021

Familial exudative vitreoretinopathy

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https://api.crossref.org/works/10.1016%2FS0161-6420%2895%2930787-7

7 January 2021

Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy

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7 January 2021

10.1016/S0161-6420(95)30787-7

Identifiers

DOI

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3 June 2018

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3 June 2018