(Q52137076)

22 April 2018

title

Autosomal dominant inheritance of a negative electroretinogram phenotype in three generations. (English)

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22 April 2018

author name string

Fitzgerald KM

1

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22 April 2018

Hashimoto T

2

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22 April 2018

Hug TE

3

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22 April 2018

Cibis GW

4

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22 April 2018

Harris DJ

5

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22 April 2018

language of work or name

English

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publication date

1 April 2001

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22 April 2018

American Journal of Ophthalmology

published in

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22 April 2018

volume

131

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22 April 2018

issue

4

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22 April 2018

page(s)

495-502

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22 April 2018

B-wave of the electroretinogram. A reflection of ON bipolar cell activity

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Comparison of the waveforms of the ON bipolar neuron and the b-wave of the electroretinogram

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Correlation of dynamic responses in the ON bipolar neuron and the b-wave of the electroretinogram

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Beta wave of the scotopic (rod) electroretinogram as a measure of the activity of human on-bipolar cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

The contribution of on-bipolar cells to the electroretinogram of rabbits and monkeys. A study using 2-amino-4-phosphonobutyrate (APB).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Specific deficit of the ON response in visual transmission by targeted disruption of the mGluR6 gene.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

The whole nucleotide sequence and chromosomal localization of the gene for human metabotropic glutamate receptor subtype 6

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype.

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

7 January 2021

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7 January 2021

Dystrophin in the retina

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Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

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

7 January 2021

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Autosomal dominant stationary night-blindness A large family rediscovered

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

A late ON response remains in visual response of the mGluR6-deficient mouse.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900849-7

10.1016/S0002-9394(00)00849-7

7 January 2021

Identifiers

DOI

1 reference

22 April 2018

1 reference

22 April 2018