Author/Creator: Zrenner, E - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Zrenner, E

1. A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosa. Issue 3 (1st March 2002)

Authors:: Dietrich, K; Jacobi, F K; Tippmann, S; Schmid, R; Zrenner, E; Wissinger, B; Apfelstedt-Sylla, E
Journal:: British journal of ophthalmology
Issue:: Volume 86:Issue 3(2002)
Page Start:: 328
Record Type:: Journal Article
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2. Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases. Issue 8 (August 1996)

Authors:: Weber, B H; Sander, S; Kopp, C; Walker, D; Eckstein, A; Wissinger, B; Zrenner, E; Grimm, T
Journal:: British journal of ophthalmology
Issue:: Volume 80:Issue 8(1996)
Page Start:: 745
Record Type:: Journal Article
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3. Cone and cone–rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation. Issue 8 (24th July 2008)

Authors:: Kitiratschky, V B D; Nagy, D; Zabel, T; Zrenner, E; Wissinger, B; Kohl, S; Jägle, H
Journal:: British journal of ophthalmology
Issue:: Volume 92:Issue 8(2008)
Page Start:: 1086
Record Type:: Journal Article
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4. Correspondence between visual and electrical input filters of ON and OFF mouse retinal ganglion cells. (12th June 2017)

Authors:: Sekhar, S; Jalligampala, A; Zrenner, E; Rathbun, D L
Journal:: Journal of neural engineering
Issue:: Volume 14:Number 4(2017:Aug.)
Page Start:
Record Type:: Journal Article
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5. Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin gene. Issue 1 (January 1995)

Authors:: Apfelstedt-Sylla, E; Theischen, M; Rüther, K; Wedemann, H; Gal, A; Zrenner, E
Journal:: British journal of ophthalmology
Issue:: Volume 79:Issue 1(1995)
Page Start:: 28
Record Type:: Journal Article
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6. Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patients. Issue 10 (28th July 2008)

Authors:: Besch, D; Sachs, H; Szurman, P; Gülicher, D; Wilke, R; Reinert, S; Zrenner, E; Bartz-Schmidt, K U; Gekeler, F
Journal:: British journal of ophthalmology
Issue:: Volume 92:Issue 10(2008)
Page Start:: 1361
Record Type:: Journal Article
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7. GPR98 mutations cause Usher syndrome type 2 in males. Issue 4 (8th April 2009)

Authors:: Ebermann, I; Wiesen, M H J; Zrenner, E; Lopez, I; Pigeon, R; Kohl, S; Löwenheim, H; Koenekoop, R K; Bolz, H J
Journal:: Journal of medical genetics
Issue:: Volume 46:Issue 4(2009)
Page Start:: 277
Record Type:: Journal Article
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8. Multifocal electroretinography in patients with Stargardt's macular dystrophy. Issue 3 (1st March 1998)

Authors:: Kretschmann, U; Seeliger, M W; Ruether, K; Usui, T; Apfelstedt-Sylla, E; Zrenner, E
Journal:: British journal of ophthalmology
Issue:: Volume 82:Issue 3(1998)
Page Start:: 267
Record Type:: Journal Article
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9. Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa. Issue 10 (16th September 2005)

Authors:: Schuster, A; Weisschuh, N; Jägle, H; Besch, D; Janecke, A R; Zierler, H; Tippmann, S; Zrenner, E; Wissinger, B
Journal:: British journal of ophthalmology
Issue:: Volume 89:Issue 10(2005)
Page Start:: 1258
Record Type:: Journal Article
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10. Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin. Issue 8 (August 1993)

Authors:: Apfelstedt-Sylla, E; Kunisch, M; Horn, M; Rüther, K; Gerding, H; Gal, A; Zrenner, E
Journal:: British journal of ophthalmology
Issue:: Volume 77:Issue 8(1993)
Page Start:: 495
Record Type:: Journal Article
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