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Results: 1-21 |
Results: 21

Authors: STROM TM NYAKATURA G APFELSTEDTSYLLA E HELLEBRAND H LORENZ B WEBER BHF WUTZ K GUTWILLINGER N RUTHER K DRESCHER B SAUER C ZRENNER E MEITINGER T ROSENTHAL A MEINDL A
Citation: Tm. Strom et al., AN L-TYPE CALCIUM-CHANNEL GENE MUTATED IN INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS, Nature genetics, 19(3), 1998, pp. 260-263

Authors: RUTHER K EHLICH P PHILIPP A ECKSTEIN A ZRENNER E
Citation: K. Ruther et al., PROGNOSTIC VALUE OF THE PATTERN ELECTRORETINOGRAM IN CASES OF TUMORS AFFECTING THE OPTIC PATHWAY, Graefe's archive for clinical and experimental ophthalmology, 236(4), 1998, pp. 259-263

Authors: SEELIGER M KRETSCHMANN U APFELSTEDTSYLLA E RUTHER K ZRENNER E
Citation: M. Seeliger et al., MULTIFOCAL ELECTRORETINOGRAPHY IN RETINITIS-PIGMENTOSA, American journal of ophthalmology, 125(2), 1998, pp. 214-226

Authors: VANDENHURK JAJM SCHWARTZ M VANBOKHOVEN H VANDEPOL TJR BOGERD L PINCKERS AJLG BLEEKERWAGEMAKERS EM PAWLOWITZKI IH RUTHER K ROPERS HH CREMERS FPM
Citation: Jajm. Vandenhurk et al., MOLECULAR-BASIS OF CHOROIDEREMIA (CHM) - MUTATIONS INVOLVING THE RAB ESCORT PROTEIN-1 (REP-1) GENE, Human mutation, 9(2), 1997, pp. 110-117

Authors: VANDENHURK JAJM HENDRIKS W VANDEPOL DJR OERLEMANS F JAISSLE G RUTHER K KOHLER K HARTMANN J ZRENNER E VANBOKHOVEN H WIERINGA B ROPERS HH CREMERS FPM
Citation: Jajm. Vandenhurk et al., MOUSE CHOROIDEREMIA GENE MUTATION CAUSES PHOTORECEPTOR CELL DEGENERATION AND IS NOT TRANSMITTED THROUGH THE FEMALE GERMLINE, Human molecular genetics, 6(6), 1997, pp. 851-858

Authors: SEELINGER M RUTHER K APFELSTEDTSYLLA E SCHLOTE W WOHLRAB M ZRENNER E
Citation: M. Seelinger et al., DIAGNOSTIC PROCEDURES AND OPHTHALMOLOGIC FINDINGS IN JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS (BATTEN-MAYOU), Der Ophthalmologe, 94(8), 1997, pp. 557-562

Authors: CREMERS FPM VANDENHURK JAJM HENDRIKS W VANDEPOL TJR OERLEMANS F JAISSLE G KOHLER K RUTHER K HARTMANN J ZRENNER E WIERINGA B ROPERS HH
Citation: Fpm. Cremers et al., THE CHOROIDEREMIA MUTATION RESULTS IN PHOTORECEPTOR CELL DEGENERATIONIN CHIMERIC MICE BUT IS EMBRYONIC LETHAL IN HEMIZYGOTIC MICE, The FASEB journal, 11(9), 1997, pp. 798-798

Authors: KREMMER S ECKSTEIN A GAL A APFELSTEDTSYLLA E WEDEMANN H RUTHER K ZRENNER E
Citation: S. Kremmer et al., OCULAR FINDINGS IN PATIENTS WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA AND CYS110PHE, ARG135GLY, AND GLN344STOP MUTATIONS OF RHODOPSIN, Graefe's archive for clinical and experimental ophthalmology, 235(9), 1997, pp. 575-583

Authors: TONNESSEN B BAATZ H RUTHER K PLEYER U HARTMANN C
Citation: B. Tonnessen et al., HEMODYNAMIC AND ELECTROPHYSIOLOGICAL PARAMETERS IN INTRAVITAL MICROSCOPY OF IRIS VESSELS, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4903-4903

Authors: KRETSCHMANN UH RUTHER K ZRENNER E
Citation: Uh. Kretschmann et al., OBSERVATIONS REGARDING THE WAVE-FORM OF THE ERG RECORDED WITH THE M-SEQUENCE STIMULATION TECHNIQUE, Investigative ophthalmology & visual science, 37(3), 1996, pp. 1591-1591

Authors: KRETSCHMANN U RUTHER K USUI T ZRENNER E
Citation: U. Kretschmann et al., ERG CAMPIMETRY USING A MULTIINPUT STIMULATION TECHNIQUE FOR MAPPING OF RETINAL FUNCTION IN THE CENTRAL VISUAL-FIELD, Ophthalmic research, 28(5), 1996, pp. 303-311

Authors: STOCKMAN A SHARPE LT RUTHER K NORDBY K
Citation: A. Stockman et al., 2 SIGNALS IN THE HUMAN ROD VISUAL-SYSTEM - A MODEL-BASED ON ELECTROPHYSIOLOGICAL DATA, Visual neuroscience, 12(5), 1995, pp. 951-970

Authors: BORTLISZ J RUTHER K MATSCHINER H HAHN M
Citation: J. Bortlisz et al., DETERMINATION OF LOW WATER CONTENTS IN DR IED SLUDGE WITH THE HELP OFFISCHER,KARL TITRATION, Acta hydrochimica et hydrobiologica, 23(3), 1995, pp. 104-110

Authors: APFELSTEDTSYLLA E THEISCHEN M RUTHER K WEDEMANN H GAL A ZRENNER E
Citation: E. Apfelstedtsylla et al., EXTENSIVE INTRAFAMILIAL AND INTERFAMILIAL PHENOTYPIC VARIATION AMONG PATIENTS WITH AUTOSOMAL-DOMINANT RETINAL DYSTROPHY AND MUTATIONS IN THE HUMAN RDS PERIPHERIN GENE, British journal of ophthalmology, 79(1), 1995, pp. 28-34

Authors: VANDENHURK J OERLEMANS F VANDEPOL D JAISSLE G RUTHER K ROPERS HH WIERINGA B CREMERS F HENDRIKS W
Citation: J. Vandenhurk et al., MATERNAL TRANSMISSION OF A CHOROIDEREMIA MUTATION IN MICE IS EMBRYONIC LETHAL, American journal of human genetics, 57(4), 1995, pp. 274-274

Authors: VANBOKHOVEN H SCHWARTZ M ANDREASSON S VANDENHURK JAJM BOGERD L JAY M RUTHER K JAY B PAWLOWITZKI IH SANKILA EM WRIGHT A ROPERS HH ROSENBERG T CREMERS FPM
Citation: H. Vanbokhoven et al., MUTATION SPECTRUM IN THE CHM GENE OF DANISH AND SWEDISH CHOROIDEREMIAPATIENTS, Human molecular genetics, 3(7), 1994, pp. 1047-1051

Authors: ECKSTEIN A ECKSTEIN S RUTHER K ZRENNER E
Citation: A. Eckstein et al., ELECTRORETINOGRAPHIC INVESTIGATION OF UNA NESTHETIZED YOUNG-CHILDREN, Klinische Monatsblatter fur Augenheilkunde, 204(2), 1994, pp. 105-110

Authors: RUTHER K EISENMANN D ZRENNER E JACOBI KW
Citation: K. Ruther et al., THE INFLUENCE OF THE DIFFRACTIVE MULTIFOC AL INTRAOCULAR-LENS ON CONTRAST SENSITIVITY, GLARE SENSITIVITY AND COLOR-VISION, Klinische Monatsblatter fur Augenheilkunde, 204(1), 1994, pp. 14-19

Authors: DEWALD G NOTHEN MM RUTHER K
Citation: G. Dewald et al., A COMMON SER THR POLYMORPHISM IN THE PERFORIN HOMOLOGOUS REGION OF HUMAN-COMPLEMENT COMPONENT C7/, Human heredity, 44(6), 1994, pp. 301-304

Authors: APFELSTEDTSYLLA E KUNISCH M HORN M RUTHER K GERDING H GAL A ZRENNER E
Citation: E. Apfelstedtsylla et al., OCULAR FINDINGS IN A FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA AND A FRAMESHIFT MUTATION ALTERING THE CARBOXYL-TERMINAL SEQUENCE OF RHODOPSIN, British journal of ophthalmology, 77(8), 1993, pp. 495-501

Authors: APFELSTEDTSYLLA E HORN M KUNISCH M RUTHER K GERDING H GAL A ZRENNER E
Citation: E. Apfelstedtsylla et al., CLINICAL CHARACTERISTICS OF AUTOSOMAL DOMINANT RETINITIS-PIGMENTOSA (ADRP) WITH A DELETION OF 8 BASE-PAIRS AND SHIFT OF THE READING FRAME IN EXON 5 OF THE RHODOPSIN GENE, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1095-1095
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