Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

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Pupillary responses in non-proliferative diabetic retinopathy.Reply: Pupil area and photopigment spectral sensitivity are relevant to study of migraine photophobia.iPhone-based Pupillometry: A Novel Approach for Assessing the Pupillary Light Reflex

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Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-sg

2016年學術文章

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2016年學術文章

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2016年學術文章

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name

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@en

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@nl

type

Item

label

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@en

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@nl

prefLabel

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@en

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@nl

P1476

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

@en

P2093

Frederick T Collison

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Gerald A Fishman

http://www.w3.org/2001/XMLSchema#string

J Jason McAnany

http://www.w3.org/2001/XMLSchema#string

Jason C Park

http://www.w3.org/2001/XMLSchema#string

P2860

The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.

Opponent melanopsin and S-cone signals in the human pupillary light response.

Effect of stimulus size and luminance on the rod-, cone-, and melanopsin-mediated pupillary light reflex

Toward a clinical protocol for assessing rod, cone, and melanopsin contributions to the human pupil response.

Excess cones in the retinal degeneration rd7 mouse, caused by the loss of function of orphan nuclear receptor Nr2e3, originate from early-born photoreceptor precursors

Full-Field Pupillary Light Responses, Luminance Thresholds, and Light Discomfort Thresholds in CEP290 Leber Congenital Amaurosis Patients

Retinal pathology of a patient with Goldmann-Favre syndrome

Nr2e3-directed transcriptional regulation of genes involved in photoreceptor development and cell-type specific phototransduction

A comprehensive analysis of sequence variants and putative disease-causing mutations in photoreceptor-specific nuclear receptor NR2E3.

P2888

s10633-016-9535-0

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157-166

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scholarly article

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10.1007/S10633-016-9535-0

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132

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Edwin M. Stone

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2016-03-31T00:00:00Z

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27033713

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6088747

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Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

about

P2860

P2860

Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.

description

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type

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932