Apfelstedt-Sylla E - Search Results

1

Molecular basis of an inherited form of incomplete achromatopsia.

Tränkner D, Jägle H, Kohl S, Apfelstedt-Sylla E, Sharpe LT, Kaupp UB, Zrenner E, Seifert R, Wissinger B. Tränkner D, et al. Among authors: apfelstedt sylla e. J Neurosci. 2004 Jan 7;24(1):138-47. doi: 10.1523/JNEUROSCI.3883-03.2004. J Neurosci. 2004. PMID: 14715947 Free PMC article.

2

Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.

Kohl S, Marx T, Giddings I, Jägle H, Jacobson SG, Apfelstedt-Sylla E, Zrenner E, Sharpe LT, Wissinger B. Kohl S, et al. Nat Genet. 1998 Jul;19(3):257-9. doi: 10.1038/935. Nat Genet. 1998. PMID: 9662398

3

Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.

Wissinger B, Jägle H, Kohl S, Broghammer M, Baumann B, Hanna DB, Hedels C, Apfelstedt-Sylla E, Randazzo G, Jacobson SG, Zrenner E, Sharpe LT. Wissinger B, et al. Genomics. 1998 Aug 1;51(3):325-31. doi: 10.1006/geno.1998.5390. Genomics. 1998. PMID: 9721202 Free article.

4

CNGA3 mutations in hereditary cone photoreceptor disorders.

Wissinger B, Gamer D, Jägle H, Giorda R, Marx T, Mayer S, Tippmann S, Broghammer M, Jurklies B, Rosenberg T, Jacobson SG, Sener EC, Tatlipinar S, Hoyng CB, Castellan C, Bitoun P, Andreasson S, Rudolph G, Kellner U, Lorenz B, Wolff G, Verellen-Dumoulin C, Schwartz M, Cremers FP, Apfelstedt-Sylla E, Zrenner E, Salati R, Sharpe LT, Kohl S. Wissinger B, et al. Am J Hum Genet. 2001 Oct;69(4):722-37. doi: 10.1086/323613. Epub 2001 Aug 30. Am J Hum Genet. 2001. PMID: 11536077 Free PMC article.

5

L- and M-cone driven ERGs are differently altered in Best's macular dystrophy.

Scholl HP, Kremers J, Apfelstedt-Sylla E, Zrenner E. Scholl HP, et al. Vision Res. 2000;40(22):3159-68. doi: 10.1016/s0042-6989(00)00160-7. Vision Res. 2000. PMID: 10996618 Free article.

6

Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.

Scholl HP, Langrová H, Pusch CM, Wissinger B, Zrenner E, Apfelstedt-Sylla E. Scholl HP, et al. Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2728-36. Invest Ophthalmol Vis Sci. 2001. PMID: 11581222

7

Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.

Ruether K, Apfelstedt-Sylla E, Zrenner E. Ruether K, et al. Ger J Ophthalmol. 1993 Nov;2(6):429-35. Ger J Ophthalmol. 1993. PMID: 8312830

8

RDS/peripherin gene mutations are frequent causes of central retinal dystrophies.

Kohl S, Christ-Adler M, Apfelstedt-Sylla E, Kellner U, Eckstein A, Zrenner E, Wissinger B. Kohl S, et al. J Med Genet. 1997 Aug;34(8):620-6. doi: 10.1136/jmg.34.8.620. J Med Genet. 1997. PMID: 9279751 Free PMC article.

9

Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.

Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E. Langrová H, et al. Among authors: apfelstedt sylla e. Vision Res. 2002 May;42(11):1475-83. doi: 10.1016/s0042-6989(02)00068-8. Vision Res. 2002. PMID: 12044753 Free article.

10

Implicit time topography of multifocal electroretinograms.

Seeliger MW, Kretschmann UH, Apfelstedt-Sylla E, Zrenner E. Seeliger MW, et al. Invest Ophthalmol Vis Sci. 1998 Apr;39(5):718-23. Invest Ophthalmol Vis Sci. 1998. PMID: 9538878

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