Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type. (Q44014596)

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9 November 2019

title

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type (English)

1 reference

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congenital stationary night blindness

9 November 2019

main subject

congenital disorder

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9 November 2019

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9 November 2019

Dorothea Besch

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9 November 2019

Eckart Apfelstedt-Sylla

series ordinal

object named as

Eckart Apfelstedt-Sylla

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9 November 2019

Daphne Gamer

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9 November 2019

Christoph Friedburg

series ordinal

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9 November 2019

publication date

1 May 2002

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9 November 2019

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9 November 2019

volume

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9 November 2019

issue

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9 November 2019

page(s)

1475-1483

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Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

9 November 2019

cites work

1 reference

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7 January 2021

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2802%2900068-8

7 January 2021

Loss of electroretinographic oscillatory potentials, optic atrophy, and dysplasia in congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2802%2900068-8

7 January 2021

Leucine-rich repeat glycoproteins of the extracellular matrix

1 reference

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7 January 2021

Models of the normal and abnormal rod system

1 reference

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7 January 2021

Off-components in response to brief light flashes in the oscillatory potential of the human electroretinogram

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2802%2900068-8

7 January 2021

Congenital stationary night blindness with negative electroretinogram. A new classification

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2802%2900068-8

7 January 2021

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2802%2900068-8

7 January 2021

On- and off-responses in the photopic electroretinogram in complete-type congenital stationary night blindness

1 reference

https://api.crossref.org/works/10.1016%2FS0042-6989%2802%2900068-8

7 January 2021

[Analysis of the human electroretinogram]

1 reference

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7 January 2021

Push-pull model of the primate photopic electroretinogram: a role for hyperpolarizing neurons in shaping the b-wave

1 reference

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7 January 2021

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

1 reference

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7 January 2021

The electroretinographic diagnosis of the incomplete form of congenital stationary night blindness

1 reference

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7 January 2021

Further studies of the chemical sensitivity of the oscillatory potentials of the electroretinogram (ERG) I. GABA- and glycine antagonists

1 reference

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7 January 2021

Further studies of the chemical sensitivity of the oscillatory potentials of the electroretinogram (ERG). II. Glutamate-aspartate-and dopamine antagonists

1 reference

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7 January 2021

Further studies of the chemical sensitivity of the oscillatory potentials of the electroretinogram (ERG). III. Some omega amino acids and ethanol

1 reference

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7 January 2021

Oscillatory potentials in the retina: what do they reveal.

1 reference

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7 January 2021

Gain of rod to horizontal cell synaptic transfer: relation to glutamate release and a dihydropyridine-sensitive calcium current

1 reference

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7 January 2021

10.1016/S0042-6989(02)00068-8

Identifiers

DOI

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9 November 2019

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