Literature DB >> 2730397

Standard for clinical electroretinography. International Standardization Committee.

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Abstract

Mesh:

Year:  1989        PMID: 2730397     DOI: 10.1001/archopht.1989.01070010838024

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


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  54 in total

1.  Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness.

Authors:  P Kenna; F Mansergh; S Millington-Ward; A Erven; R Kumar-Singh; R Brennan; G J Farrar; P Humphries
Journal:  Br J Ophthalmol       Date:  1997-03       Impact factor: 4.638

2.  Influence of axial length of normal eyes on PERG.

Authors:  Rudy Hidajat; Jan Mclay; Celeste Burley; Mark Elder; Jason Morton; David Goode
Journal:  Doc Ophthalmol       Date:  2003-09       Impact factor: 2.379

3.  Absence of ocular interaction in flicker ERG responses reflecting cone opponent and luminance signals.

Authors:  Mirella Telles Salgueiro Barboni; Dora Fix Ventura; Jan Kremers
Journal:  Doc Ophthalmol       Date:  2010-04-01       Impact factor: 2.379

4.  Carbamylated erythropoietin mediates retinal neuroprotection in streptozotocin-induced early-stage diabetic rats.

Authors:  Xiaojing Liu; Bijun Zhu; Haidong Zou; Daode Hu; Qing Gu; Kun Liu; Xun Xu
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2015-03-01       Impact factor: 3.117

5.  Severe autosomal recessive retinitis pigmentosa maps to chromosome 1p13.3-p21.2 between D1S2896 and D1S457 but outside ABCA4.

Authors:  Qingjiong Zhang; Fareeha Zulfiqar; Xueshan Xiao; S Amer Riazuddin; Radha Ayyagari; Farooq Sabar; Raphael Caruso; Paul A Sieving; Sheikh Riazuddin; J Fielding Hejtmancik
Journal:  Hum Genet       Date:  2005-09-28       Impact factor: 4.132

6.  Human cerebral activation during steady-state visual-evoked responses.

Authors:  Maria A Pastor; Julio Artieda; Javier Arbizu; Miguel Valencia; Jose C Masdeu
Journal:  J Neurosci       Date:  2003-12-17       Impact factor: 6.167

7.  Clinical features of a Japanese family with autosomal dominant retinitis pigmentosa associated with a Thr494Met mutation in the HPRP3 gene.

Authors:  Yuko Wada; Toshitaka Itabashi; Hajime Sato; Makoto Tamai
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-04-15       Impact factor: 3.117

8.  Severe course of cutaneous melanoma associated paraneoplastic retinopathy.

Authors:  U Kellner; N Bornfeld; M H Foerster
Journal:  Br J Ophthalmol       Date:  1995-08       Impact factor: 4.638

9.  In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier.

Authors:  Jeremy C Kallman; James O Phillips; Naomi F Bramhall; John P Kelly; Valerie A Street
Journal:  Otol Neurotol       Date:  2008-09       Impact factor: 2.311

10.  Electroretinographic assessment of early retinopathy in rats.

Authors:  T Maertins; F Kroetlinger; E Sander; J Pauluhn; L Machemer
Journal:  Arch Toxicol       Date:  1993       Impact factor: 5.153

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