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Gabe von Vitamin-A-Derivaten bei erblichen Netzhautdegenerationen : Stand der Empfehlungen = Dosage of vatamin-A derivatives in hereditary retinal degeneration. Current recommendationsZRENNER, E; RÜTHER, K.Der Ophthalmologe (Berlin. Print). 2001, Vol 98, Num 6, pp 526-528, issn 0941-293XArticle

Entwicklungen in der ophthalmologischen Elektrophysiologie = Developments in ophtalmic electrophysiologyRüTHER, K; ZRENNER, E.Klinische Monatsblätter für Augenheilkunde. 1993, Vol 202, Num 2, pp 140-145, issn 0023-2165Article

A new polymorphic probe on 5q11.2 - 13.3: ECB306Bgl2.1 (D5S215)RÜTHER, K; WIRTH, B.Nucleic acids research. 1992, Vol 20, Num 5, issn 0305-1048, p. 1160Article

Evaluation of risk factors for retinal damage due to chloroquine and hydroxychloroquineBERGHOLZ, R; SCHROETER, J; RUTHER, K et al.British journal of ophthalmology. 2010, Vol 94, Num 12, pp 1637-1642, issn 0007-1161, 6 p.Article

Retinitis pigmentosa, Klinische Befunde, molekulargenetische Ergebnisse und Forschungsperspektiven = Retinitis pigmentosa: clinical findings, molecular genetic results and research perspectivesZRENNER, E; RÜTHER, K; APFELSTEDT-SYLLA, E et al.(Der) Ophthalmologe. 1992, Vol 89, Num 1, pp 5-21Article

Wirkung von Kantenfiltern auf die Kontrastwahrnehmung bei Retinitis pigmentosa = Retinitis pigmentosa : effects of cut-off filters on contrast sensitivityRÜTHER, K; VON GRUBEN, C; ZRENNER, E et al.Fortschritte der Ophthalmologie. 1991, Vol 88, Num 6, pp 829-832, issn 0723-8045Conference Paper

Beidseitige Optikusartrophie und langsame Sehverschlechterung = Alagille syndrome with ocular complicationLECHNER, S; RÜTHER, K; HARTMANN, C et al.Der Ophthalmologe (Berlin. Print). 2001, Vol 98, Num 10, pp 988-989, issn 0941-293XArticle

Are vigabatrin-associated visual field constrictions asymptomatic?SCHMIDT, T; RÜTHER, K; SCHMITZ, B et al.Journal of neurology. 2004, Vol 251, Num 7, pp 887-888, issn 0340-5354, 2 p.Article

Zur klinischen Bedeutung der objektiven Sehschärfenschätzung mit Hilfe der visuell evozierten kortikalen Potentiale durch schnelle Reizmustersequenzen unterschiedlicher Ortsfrequenz = Objective assessment of visual acuity using visually evoked potentials in response to fast sequences of pattern stimuli of different spatial frequency : a study to determine the clinical relevanceHEINE, S; RÜTHER, K; ISENSEE, J et al.Klinische Monatsblätter für Augenheilkunde. 1999, Vol 215, Num 3, pp 175-181, issn 0023-2165Article

Der Einfluss diffraktiver Multifokallinsen auf Kontrastsehen, Gegenlichtsehschärfe and Farbsinn = The influence of the diffractive multifocal intraocular lens on contrast sensitivity, glare sensitivity and colour visionRÜTHER, K; EISENMANN, D; ZRENNER, E et al.Klinische Monatsblätter für Augenheilkunde. 1994, Vol 204, Num 1, pp 14-19, issn 0023-2165Article

Two signals in the human rod visual system : a model based on electrophysiological dataSTOCKMAN, A; SHARPE, L. T; RÜTHER, K et al.Visual neuroscience (Print). 1995, Vol 12, Num 5, pp 951-970, issn 0952-5238Article

Is visual field constriction in epilepsy patients treated with vigabatrin reversible?SCHMIDT, T; RÜTHER, K; JOKIEL, B et al.Journal of neurology. 2002, Vol 249, Num 8, pp 1066-1071, issn 0340-5354, 6 p.Article

Juvenile neuronale Zeroidlipofuszinose (Batten-Mayou) : Augenärztliche Diagnostik und Befunde = Diagnostic procedures and ophthalmologic findings in juvenile neuronal ceroid lipofuscinosis (Batten-Mayou)SEELIGER, M; RÜTHER, K; APFELSTEDT-SYLLA, E et al.Der Ophthalmologe (Berlin. Print). 1997, Vol 94, Num 8, pp 557-562, issn 0941-293XConference Paper

Extensive intrafamilial and interfamilial phenotypic variation among patients with autosomal dominant retinal dystrophy and mutations in the human RDS/peripherin geneAPFELSTEDT-SYLLA, E; THEISCHEN, M; RÜTHER, K et al.British journal of ophthalmology. 1995, Vol 79, Num 1, pp 28-34, issn 0007-1161Article

Visual field constriction in epilepsy patients treated with vigabatrin and other antiepileptic drugs: A prospective studySCHMITZ, B; SCHMIDT, T; JOKIEL, B et al.Journal of neurology. 2002, Vol 249, Num 4, pp 469-475, issn 0340-5354Article

Protracted course of juvenile ceroid lipofuscinosis associated with a novel CLN3 mutation (p.Y199X)SARPONG, A; SCHOTTMANN, G; RÜTHER, K et al.Clinical genetics. 2009, Vol 76, Num 1, pp 38-45, issn 0009-9163, 8 p.Article

Multifocal electroretinography in retinitis pigmentosaSEELIGER, M; KRETSCHMANN, U; APFELSTEDT-SYLLA, E et al.American journal of ophthalmology. 1998, Vol 125, Num 2, pp 214-226, issn 0002-9394Article

Sozialophthalmologische Aspekte bei Retinitis pigmentosa : Netzhaut/Aderhaut : Glaskörper = Social service aspects in retinitis pigmentosaRÜTHER, K; BANHART, F; KREMMER, S et al.Der Ophthalmologe (Berlin. Print). 1995, Vol 92, Num 5, pp 704-707, issn 0941-293XConference Paper

Klinische Elektroretinographie : Standardprotokoll und Normwerte = Clinical electroretinography: standardized protocol and normal valuesJACOBI, P. C; RÜTHER, K; MILICZEK, K.-D et al.Klinische Monatsblätter für Augenheilkunde. 1993, Vol 202, Num 1, pp 27-42, issn 0023-2165Article

Choroideremia-locus maps between DXS3 and DXS11 on XqGAL, A; BRUNSMANN, F; HOGENKAMP, D et al.Human genetics. 1986, Vol 73, Num 2, pp 123-126, issn 0340-6717Article

Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsinAPFELSTEDT-SYLLA, E; KUNISCH, M; HORN, M et al.British journal of ophthalmology. 1993, Vol 77, Num 8, pp 495-501, issn 0007-1161Article

Ocular findings in patients with autosomal dominant retinitis pigmentosa and Cys110Phe, Arg135Gly, and GIn344stop mutations of rhodopsinKREMMER, S; ECKSTEIN, A; GAL, A et al.Graefe's archive for clinical and experimental ophthalmology. 1997, Vol 235, Num 9, pp 575-583, issn 0721-832XConference Paper

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindnessSTROM, T. M; NYAKATURA, G; SAUER, C et al.Nature genetics. 1998, Vol 19, Num 3, pp 260-263, issn 1061-4036Article

Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patientsVAN BOKHOVEN, H; SCHWARTZ, M; WRIGHT, A et al.Human molecular genetics (Print). 1994, Vol 3, Num 7, pp 1047-1051, issn 0964-6906Article