PubMed

A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder.

Littink KW, van Genderen MM, Collin RW, Roosing S, de Brouwer AP, Riemslag FC, Venselaar H, Thiadens AA, Hoyng CB, Rohrschneider K, den Hollander AI, Cremers FP, van den Born LI.

Invest Ophthalmol Vis Sci. 2009 May;50(5):2344-50. Epub 2008 Dec 13.PMID: 19074807 [PubMed - indexed for MEDLINE]Related articles

Use of fundus perimetry (microperimetry) to quantify macular sensitivity.

Rohrschneider K, Bültmann S, Springer C.

Prog Retin Eye Res. 2008 Sep;27(5):536-48. Epub 2008 Aug 3. Review.PMID: 18723109 [PubMed - indexed for MEDLINE]Related articles

[Coats' disease. Important differential diagnosis for retinoblastoma]

Förl B, Schmack I, Grossniklaus HE, Rohrschneider K.

Ophthalmologe. 2008 Aug;105(8):761-4. German. PMID: 18299842 [PubMed - indexed for MEDLINE]Related articles

Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.

den Hollander AI, Lopez I, Yzer S, Zonneveld MN, Janssen IM, Strom TM, Hehir-Kwa JY, Veltman JA, Arends ML, Meitinger T, Musarella MA, van den Born LI, Fishman GA, Maumenee IH, Rohrschneider K, Cremers FP, Koenekoop RK.

Invest Ophthalmol Vis Sci. 2007 Dec;48(12):5690-8.PMID: 18055821 [PubMed - indexed for MEDLINE]Related articlesFree article

Microperimetric assessment of patients with type 2 idiopathic macular telangiectasia.

Charbel Issa P, Helb HM, Rohrschneider K, Holz FG, Scholl HP.

Invest Ophthalmol Vis Sci. 2007 Aug;48(8):3788-95.PMID: 17652753 [PubMed - indexed for MEDLINE]Related articlesFree article

[Fundamentals for the medical evaluation of handicapped people in legislation]

Rohrschneider K, Bültmann S, Mackensen I.

Ophthalmologe. 2007 Jun;104(6):457-63. German. PMID: 17505834 [PubMed - indexed for MEDLINE]Related articles

[Errors and difficulties in the assessment of severely handicapped and blind persons]

Mackensen I, Becker S, Rohrschneider K.

Ophthalmologe. 2007 Jun;104(6):464, 466-73. German. PMID: 17505833 [PubMed - indexed for MEDLINE]Related articles

[Determination of visual function in legal assessment]

Springer C, Bültmann S, Krastel H, Rohrschneider K.

Ophthalmologe. 2007 Jun;104(6):474-9. German. PMID: 17505832 [PubMed - indexed for MEDLINE]Related articles

[Introduction to the topic: medial evaluation of severely handicapped and blind persons in legislation]

Rohrschneider K.

Ophthalmologe. 2007 Jun;104(6):455-6. German. No abstract available. PMID: 17505831 [PubMed - indexed for MEDLINE]Related articles

Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis.

den Hollander AI, Koenekoop RK, Yzer S, Lopez I, Arends ML, Voesenek KE, Zonneveld MN, Strom TM, Meitinger T, Brunner HG, Hoyng CB, van den Born LI, Rohrschneider K, Cremers FP.

Am J Hum Genet. 2006 Sep;79(3):556-61. Epub 2006 Jul 11.PMID: 16909394 [PubMed - indexed for MEDLINE]Related articlesFree article

[Central serous chorioretinopathy--retinal function and morphology: microperimetry and optical coherence tomography]

Springer C, Völcker HE, Rohrschneider K.

Ophthalmologe. 2006 Sep;103(9):791-7. German. PMID: 16874536 [PubMed - indexed for MEDLINE]Related articles

Autologous translocation of the choroid and retinal pigment epithelium in age-related macular degeneration.

Joussen AM, Heussen FM, Joeres S, Llacer H, Prinz B, Rohrschneider K, Maaijwee KJ, van Meurs J, Kirchhof B.

Am J Ophthalmol. 2006 Jul;142(1):17-30.PMID: 16815247 [PubMed - indexed for MEDLINE]Related articles

Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis.

Yzer S, Leroy BP, De Baere E, de Ravel TJ, Zonneveld MN, Voesenek K, Kellner U, Ciriano JP, de Faber JT, Rohrschneider K, Roepman R, den Hollander AI, Cruysberg JR, Meire F, Casteels I, van Moll-Ramirez NG, Allikmets R, van den Born LI, Cremers FP.

Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1167-76.PMID: 16505055 [PubMed - indexed for MEDLINE]Related articlesFree article

[Static fundus perimetry in experimental subjects. Microperimeter 1 versus SLO]

Springer C, Völcker HE, Rohrschneider K.

Ophthalmologe. 2006 Mar;103(3):214-20. German. PMID: 16091926 [PubMed - indexed for MEDLINE]Related articles

Late-onset retinal dystrophy in alpha-mannosidosis.

Springer C, Gutschalk A, Meinck HM, Rohrschneider K.

Graefes Arch Clin Exp Ophthalmol. 2005 Dec;243(12):1277-9. Epub 2005 Jun 17.PMID: 16075219 [PubMed - indexed for MEDLINE]Related articles

Fundus perimetry with the Micro Perimeter 1 in normal individuals: comparison with conventional threshold perimetry.

Springer C, Bültmann S, Völcker HE, Rohrschneider K.

Ophthalmology. 2005 May;112(5):848-54.PMID: 15878065 [PubMed - indexed for MEDLINE]Related articles

Characterization of the Crumbs homolog 2 (CRB2) gene and analysis of its role in retinitis pigmentosa and Leber congenital amaurosis.

van den Hurk JA, Rashbass P, Roepman R, Davis J, Voesenek KE, Arends ML, Zonneveld MN, van Roekel MH, Cameron K, Rohrschneider K, Heckenlively JR, Koenekoop RK, Hoyng CB, Cremers FP, den Hollander AI.

Mol Vis. 2005 Apr 15;11:263-73.PMID: 15851977 [PubMed - indexed for MEDLINE]Related articlesFree article

Microperimetry--comparison between the micro perimeter 1 and scanning laser ophthalmoscope--fundus perimetry.

Rohrschneider K, Springer C, Bültmann S, Völcker HE.

Am J Ophthalmol. 2005 Jan;139(1):125-34.PMID: 15672526 [PubMed - indexed for MEDLINE]Related articles

[Influence of cutoff filters on reading behavior in age-related macular degeneration]

Rohrschneider K, Stritzke M, Ziese D, Bayer Y.

Ophthalmologe. 2005 Jul;102(7):692-7. German. PMID: 15662502 [PubMed - indexed for MEDLINE]Related articles

Fundus autofluorescence and fundus perimetry in the junctional zone of geographic atrophy in patients with age-related macular degeneration.

Schmitz-Valckenberg S, Bültmann S, Dreyhaupt J, Bindewald A, Holz FG, Rohrschneider K.

Invest Ophthalmol Vis Sci. 2004 Dec;45(12):4470-6. Erratum in: Invest Ophthalmol Vis Sci. 2005 Jan;46(1):7. PMID: 15557456 [PubMed - indexed for MEDLINE]Related articlesFree article

Adult alpha-mannosidosis: clinical progression in the absence of demyelination.

Gutschalk A, Harting I, Cantz M, Springer C, Rohrschneider K, Meinck HM.

Neurology. 2004 Nov 9;63(9):1744-6.PMID: 15534274 [PubMed - indexed for MEDLINE]Related articles

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone-rod dystrophy and retinitis pigmentosa.

Klevering BJ, Yzer S, Rohrschneider K, Zonneveld M, Allikmets R, van den Born LI, Maugeri A, Hoyng CB, Cremers FP.

Eur J Hum Genet. 2004 Dec;12(12):1024-32.PMID: 15494742 [PubMed - indexed for MEDLINE]Related articlesFree article

Determination of the location of the fovea on the fundus.

Rohrschneider K.

Invest Ophthalmol Vis Sci. 2004 Sep;45(9):3257-8.PMID: 15326148 [PubMed - indexed for MEDLINE]Related articlesFree article

[Epidemiology of blindness in Baden, Germany]

Rohrschneider K, Greim S.

Klin Monbl Augenheilkd. 2004 Feb;221(2):116-21. German. PMID: 14986210 [PubMed - indexed for MEDLINE]Related articles

Functional changes measured with SLO in idiopathic macular holes and in macular changes secondary to premacular fibrosis. Function in macular holes.

Rohrschneider K, Bültmann S, Kruse FE, Völcker HE.

Int Ophthalmol. 2001;24(4):177-84.PMID: 12678392 [PubMed - indexed for MEDLINE]Related articles

[Diagnosis and follow-up in glaucoma patients using the Heidelberg retina tomograph]

Scheuerle AF, Schmidt E, Kruse FE, Rohrschneider K.

Ophthalmologe. 2003 Jan;100(1):5-12. German. PMID: 12557020 [PubMed - indexed for MEDLINE]Related articles

Reproducibility of multifocal ERG using the scanning laser ophthalmoscope.

Bültmann S, Rohrschneider K.

Graefes Arch Clin Exp Ophthalmol. 2002 Oct;240(10):841-5. Epub 2002 Sep 21.PMID: 12397433 [PubMed - indexed for MEDLINE]Related articles

[Follow-up on MEWDS by fundus perimetry and multifocal ERG with the SLO]

Bültmann S, Martin M, Rohrschneider K.

Ophthalmologe. 2002 Sep;99(9):719-23. German. PMID: 12219262 [PubMed - indexed for MEDLINE]Related articles

[Diagnosis of retinal diseases. Comparison between multifocal ERG and fundus perimetry - a case study]

Rohrschneider K, Bültmann S, Kiel R, Weimer P, Krastel H, Blankenagel A.

Ophthalmologe. 2002 Sep;99(9):695-702. German. PMID: 12219258 [PubMed - indexed for MEDLINE]Related articles

[Satisfaction with low vision aids]

Rohrschneider K, Kiel R, Pavlovska V, Blankenagel A.

Klin Monbl Augenheilkd. 2002 Jul;219(7):507-11. German. PMID: 12195316 [PubMed - indexed for MEDLINE]Related articles

Prevalence and geographical distribution of Usher syndrome in Germany.

Spandau UH, Rohrschneider K.

Graefes Arch Clin Exp Ophthalmol. 2002 Jun;240(6):495-8. Epub 2002 May 23.PMID: 12107518 [PubMed - indexed for MEDLINE]Related articles

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

Astuto LM, Bork JM, Weston MD, Askew JW, Fields RR, Orten DJ, Ohliger SJ, Riazuddin S, Morell RJ, Khan S, Riazuddin S, Kremer H, van Hauwe P, Moller CG, Cremers CW, Ayuso C, Heckenlively JR, Rohrschneider K, Spandau U, Greenberg J, Ramesar R, Reardon W, Bitoun P, Millan J, Legge R, Friedman TB, Kimberling WJ.

Am J Hum Genet. 2002 Aug;71(2):262-75. Epub 2002 Jun 19.PMID: 12075507 [PubMed - indexed for MEDLINE]Related articlesFree article

Phenotypic spectrum of autosomal recessive cone-rod dystrophies caused by mutations in the ABCA4 (ABCR) gene.

Klevering BJ, Blankenagel A, Maugeri A, Cremers FP, Hoyng CB, Rohrschneider K.

Invest Ophthalmol Vis Sci. 2002 Jun;43(6):1980-5.PMID: 12037008 [PubMed - indexed for MEDLINE]Related articlesFree article

Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene.

den Hollander AI, Heckenlively JR, van den Born LI, de Kok YJ, van der Velde-Visser SD, Kellner U, Jurklies B, van Schooneveld MJ, Blankenagel A, Rohrschneider K, Wissinger B, Cruysberg JR, Deutman AF, Brunner HG, Apfelstedt-Sylla E, Hoyng CB, Cremers FP.

Am J Hum Genet. 2001 Jul;69(1):198-203. Epub 2001 May 24. Erratum in: Am J Hum Genet 2001 Nov;69(5):1160. PMID: 11389483 [PubMed - indexed for MEDLINE]Related articlesFree article

[Fundus-controlled functional evaluation in macular diseases with the scanning laser ophthalmoscope]

Rohrschneider K, Bültmann S.

Ophthalmologe. 2001 Jan;98(1):3-9. German. PMID: 11220268 [PubMed - indexed for MEDLINE]Related articles

[Ab interno trabeculectomy with the Nd:YLF picosecond laser]

Rohrschneider K, Kruse FE, Kessler R, Gölz S, Bille JF, Völcker HE.

Ophthalmologe. 2000 Nov;97(11):748-52. German. PMID: 11130162 [PubMed - indexed for MEDLINE]Related articles

Treatment of corneal neovascularization with dietary isoflavonoids and flavonoids.

Joussen AM, Rohrschneider K, Reichling J, Kirchhof B, Kruse FE.

Exp Eye Res. 2000 Nov;71(5):483-7.PMID: 11040083 [PubMed - indexed for MEDLINE]Related articles

[Painless orbital swelling after sojourn in tropics. Cysticercosis and other parasitic eye diseases]

Wabbels B, Kruse F, Helmke B, Rohrschneider K, Völcker HE.

Klin Monbl Augenheilkd. 2000 Aug;217(2):109-13. Review. German. PMID: 11022665 [PubMed - indexed for MEDLINE]Related articles

[Utilization of a new night vision enhancement device (DAVIS)]

Rohrschneider K, Spandau U, Wechsler S, Blankenagel A.

Klin Monbl Augenheilkd. 2000 Aug;217(2):88-93. German. PMID: 11022662 [PubMed - indexed for MEDLINE]Related articles

[Ophthalmologic emergencies]

Kruse FE, Rohrschneider K, Völcker HE.

Internist (Berl). 2000 Aug;41(8):733-5. Review. German. No abstract available. PMID: 10986657 [PubMed - indexed for MEDLINE]Related articles

Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.

Maugeri A, Klevering BJ, Rohrschneider K, Blankenagel A, Brunner HG, Deutman AF, Hoyng CB, Cremers FP.

Am J Hum Genet. 2000 Oct;67(4):960-6. Epub 2000 Aug 24.PMID: 10958761 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration.

Krämer F, White K, Pauleikhoff D, Gehrig A, Passmore L, Rivera A, Rudolph G, Kellner U, Andrassi M, Lorenz B, Rohrschneider K, Blankenagel A, Jurklies B, Schilling H, Schütt F, Holz FG, Weber BH.

Eur J Hum Genet. 2000 Apr;8(4):286-92.PMID: 10854112 [PubMed - indexed for MEDLINE]Related articlesFree article

Stereotactic radiation therapy for malignant choroidal tumors: preliminary, short-term results.

Bellmann C, Fuss M, Holz FG, Debus J, Rohrschneider K, Völcker HE, Wannenmacher M.

Ophthalmology. 2000 Feb;107(2):358-65.PMID: 10690839 [PubMed - indexed for MEDLINE]Related articles

Cryopreserved human amniotic membrane for ocular surface reconstruction.

Kruse FE, Joussen AM, Rohrschneider K, You L, Sinn B, Baumann J, Völcker HE.

Graefes Arch Clin Exp Ophthalmol. 2000 Jan;238(1):68-75.PMID: 10664056 [PubMed - indexed for MEDLINE]Related articles

Scanning laser ophthalmoscope fundus perimetry before and after laser photocoagulation for clinically significant diabetic macular edema.

Rohrschneider K, Bültmann S, Glück R, Kruse FE, Fendrich T, Völcker HE.

Am J Ophthalmol. 2000 Jan;129(1):27-32.PMID: 10653409 [PubMed - indexed for MEDLINE]Related articles

[Techniques for reconstruction of the corneal surface by transplantation of preserved human amniotic membrane]

Kruse FE, Rohrschneider K, Völcker HE.

Ophthalmologe. 1999 Oct;96(10):673-8. German. PMID: 10552162 [PubMed - indexed for MEDLINE]Related articles

[Ophthalmological rehabilitation - experience at the University Eye Hospital Heidelberg]

Rohrschneider K, Bruder I, Blankenagel A.

Ophthalmologe. 1999 Sep;96(9):611-6. German. PMID: 10501991 [PubMed - indexed for MEDLINE]Related articles

Multilayer amniotic membrane transplantation for reconstruction of deep corneal ulcers.

Kruse FE, Rohrschneider K, Völcker HE.

Ophthalmology. 1999 Aug;106(8):1504-10; discussion 1511.PMID: 10442895 [PubMed - indexed for MEDLINE]Related articles

[Experimental external irradiation of corneal neovascularization]

Joussen AM, Kruse FE, Otzel D, Holz FG, Debus J, Rohrschneider K, Völcker HE.

Ophthalmologe. 1999 Apr;96(4):234-9. German. PMID: 10409850 [PubMed - indexed for MEDLINE]Related articles

The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt disease.

Maugeri A, van Driel MA, van de Pol DJ, Klevering BJ, van Haren FJ, Tijmes N, Bergen AA, Rohrschneider K, Blankenagel A, Pinckers AJ, Dahl N, Brunner HG, Deutman AF, Hoyng CB, Cremers FP.

Am J Hum Genet. 1999 Apr;64(4):1024-35.PMID: 10090887 [PubMed - indexed for MEDLINE]Related articlesFree article