(Q45169735)

10 December 2017

title

Spinocerebellar degeneration with negative electroretinogram: dysfunction of the bipolar cells (English)

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10 December 2017

Akio Kimura

1

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10 December 2017

Hideaki Nemoto

2

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10 December 2017

Jin Nishimiya

3

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10 December 2017

Tatuhiko Yuasa

4

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10 December 2017

Hiroko Yamazaki

5

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10 December 2017

publication date

1 May 2004

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Documenta Ophthalmologica

10 December 2017

published in

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10 December 2017

volume

108

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10 December 2017

issue

3

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10 December 2017

page(s)

241-247

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https://scigraph.springernature.com/pub.10.1007/s10633-004-1042-z

10 December 2017

exact match

0 references

cites work

Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness

1 reference

12 December 2020

A case of cerebellar degeneration with schizophrenia-like psychosis, severe iron deficiency, hypoceruloplasminemia and abnormal electroretinography: a new syndrome?

1 reference

12 December 2020

The incidence of negative ERG in clinical practice

1 reference

12 December 2020

Partially deficient glutamate dehydrogenase activity and attenuated oscillatory potentials in patients with spinocerebellar degeneration

1 reference

12 December 2020

Congenital stationary night blindness with negative electroretinogram. A new classification

1 reference

12 December 2020

Standard for clinical electroretinography (1999 update). International Society for Clinical Electrophysiology of Vision.

1 reference

12 December 2020

Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotype

1 reference

12 December 2020

Olivopontocerebellar atrophy with retinal degeneration. An electroretinographic and histopathologic investigation

1 reference

12 December 2020

Possible pathogenesis of congenital stationary night blindness.

1 reference

12 December 2020

Olivopontocerebellar atrophy with retinal degeneration. A clinical and ocular histopathologic study

1 reference

12 December 2020

Ophthalmologic findings in patients with ataxia

1 reference

12 December 2020

Cone dysfunction in a subgroup of patients with autosomal dominant cerebellar ataxia

1 reference

12 December 2020

10.1007/S10633-004-1042-Z

Identifiers

DOI

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Dimensions Publication ID

10 December 2017

1006390290

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1 reference