(Q44795752)

6 December 2017

Hereditary retinochoroidal dystrophies. Part 2: differential diagnosis (English)

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6 December 2017

U Kellner

1

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6 December 2017

A B Renner

series ordinal

2

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6 December 2017

H Tillack

series ordinal

3

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6 December 2017

language of work or name

German

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publication date

1 April 2004

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6 December 2017

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6 December 2017

101

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6 December 2017

4

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6 December 2017

397-412; quiz 413-4

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https://scigraph.springernature.com/pub.10.1007/s00347-003-0945-5

6 December 2017

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cites work

Visual function in patients with cone-rod dystrophy (CRD) associated with mutations in the ABCA4(ABCR) gene

1 reference

12 December 2020

X linked retinoschisis

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12 December 2020

Bardet-Biedl syndrome and Usher syndrome

1 reference

12 December 2020

Visual acuity loss and clinical observations in a large series of patients with Stargardt disease.

1 reference

12 December 2020

Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy

1 reference

12 December 2020

Molecular genetics of Leber congenital amaurosis

1 reference

12 December 2020

Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene

1 reference

12 December 2020

Infantile and childhood retinal blindness: a molecular perspective (The Franceschetti Lecture)

1 reference

12 December 2020

Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation

1 reference

12 December 2020

Molecular genetics of Oguchi disease, fundus albipunctatus, and other forms of stationary night blindness: LVII Edward Jackson Memorial Lecture.

1 reference

12 December 2020

Usher syndrome in the city of Birmingham--prevalence and clinical classification

1 reference

12 December 2020

Clinical and electrophysiological findings in autosomal dominant vitreoretinochoroidopathy: report of a new pedigree

1 reference

12 December 2020

Phenocopies of hereditary retinal degenerations

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12 December 2020

Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns.

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12 December 2020

Cone deactivation kinetics and GRK1/GRK7 expression in enhanced S cone syndrome caused by mutations in NR2E3.

1 reference

12 December 2020

Hereditary retinochoroidal dystrophies. Part 1: Pathogenesis, diagnosis, therapy and patient counselling

1 reference

12 December 2020

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia

1 reference

12 December 2020

Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome

1 reference

12 December 2020

The gene for Stargardt disease, ABCA4, is a major retinal gene: a mini-review

1 reference

12 December 2020

Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase

1 reference

12 December 2020

Refsum's disease: a peroxisomal disorder affecting phytanic acid alpha-oxidation

1 reference

12 December 2020

The molecular genetics of Usher syndrome

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12 December 2020

Pattern dystrophy of the retinal pigment epithelium and geographic atrophy of the macula

1 reference

12 December 2020

10.1007/S00347-003-0945-5

Identifiers

DOI

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6 December 2017

1 reference