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    1. Pesch, K; Tomiuk, J; Broghammer, M; Zrenner, E; Apfelstedt-Sylla, E; Jacobi, FK; Wissinger, B; Pusch, CM
      Case populations must match the respective disease model: Genotype diversity causes linkage disequilibrium mapping failure in monogenic disorders

      INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
    2. Seeliger, MW; Grimm, C; Stahlberg, F; Friedburg, C; Jaissle, G; Zrenner, E; Guo, H; Reme, CE; Humphries, P; Hofmann, F; Biel, M; Fariss, RN; Redmond, TM; Wenzel, A
      New views on RPE65 deficiency: the rod system is the source of vision in amouse model of Leber congenital amaurosis

      NATURE GENETICS
    3. Pesch, UEA; Leo-Kottler, B; Mayor, S; Jurklies, B; Kellner, U; Apfelstedt-Sylla, E; Zrenner, E; Alexander, C; Wissinger, B
      OPA1 mutations in patients with autosomal dominant optic atrophy and evidence for semi-dominant inheritance

      HUMAN MOLECULAR GENETICS
    4. Rejdak, R; Zarnowski, T; Turski, WA; Okuno, E; Kocki, T; Zagorski, Z; Kohler, K; Guenther, E; Zrenner, E
      Presence of kynurenic acid and kynurenine aminotransferases in the inner retina

      NEUROREPORT
    5. Zrenner, E; Ruther, K
      Dosage of vitamin-A derivatives in hereditary retinal degeneration. Current recommendations

      OPHTHALMOLOGE
    6. Zrenner, E; Gekeler, F; Gabel, VP; Graf, HG; Graf, M; Guenther, E; Haemmerle, H; Hoefflinger, B; Kobuch, K; Kohler, K; Nisch, W; Sachs, H; Schlosshauer, B; Schubert, M; Schwahn, H; Stelzle, M; Stett, A; Troeger, B; Weiss, S
      Subretinal microphotodiode arrays to replace degenerated photoreceptors?

      OPHTHALMOLOGE
    7. Kohler, K; Hartmann, JA; Werts, D; Zrenner, E
      Retinal degeneration and biocompatibility of subretinal implants: a histological analysis

      OPHTHALMOLOGE
    8. Eckhorn, R; Stett, A; Schanze, T; Gekeler, F; Schwahn, H; Zrenner, E; Wilms, M; Eger, M; Hesse, L
      Physiological testing of function of retinal implants with animal models

      OPHTHALMOLOGE
    9. Jurklies, B; Weismann, M; Kellner, U; Zrenner, E; Bornfeld, N
      Clinical findings in autosomal recessive enhanced S-cone sensitivity syndrome

      OPHTHALMOLOGE
    10. Scholl, HPN; Langrova, H; Weber, BHF; Zrenner, E; Apfelstedt-Sylla, E
      Clinical electrophysiology of two rod pathways: normative values and clinical application

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    11. Erb, C; Voelker, W; Adler, M; Wohlrab, M; Zrenner, E
      Color-vision disturbances in patients with coronary artery disease

      COLOR RESEARCH AND APPLICATION
    12. Rizzo, JF; Wyatt, J; Humayun, M; de Juan, E; Liu, WT; Chow, A; Eckmiller, R; Zrenner, E; Yagi, T; Abrams, G
      Retinal prosthesis - An encouraging first decade with major challenges ahead

      OPHTHALMOLOGY
    13. Wenzel, A; Grimm, C; Seeliger, MW; Jaissle, G; Hafezi, F; Kretschmer, R; Zrenner, E; Reme, CE
      Prevention of photoreceptor apoptosis by activation of the glucocorticoid receptor

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    14. Jacobi, FK; Leo-Kottler, B; Mittelviefhaus, K; Zrenner, E; Meyer, J; Pusch, CM; Wissinger, B
      Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    15. Jaissle, GB; May, CA; Reinhard, J; Kohler, K; Fauser, S; Lutjen-Drecoll, E; Zrenner, E; Seeliger, MW
      Evaluation of the rhodopsin knockout mouse as a model of pure cone function

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    16. Seeliger, MW; Zrenner, E; Apfelstedt-Sylla, E; Jaissle, GB
      Identification of Usher syndrome subtypes by ERG implicit time

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    17. Scholl, HPN; Langrova, H; Pusch, CM; Wissinger, B; Zrenner, E; Apfelstedt-Sylla, E
      Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    18. Wilhelm, B; Ludtke, H; Peters, T; Schmid, R; Wilhelm, H; Zrenner, E
      Automated swinging flashlight test in patients with optic nerve disorders

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    19. Wissinger, B; Gamer, D; Jagle, 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, FPM; Apfelstedt-ylla, E; Zrenner, E; Salati, R; Sharpe, LT; Kohl, S
      CNGA3 mutations in hereditary cone photoreceptor disorders

      AMERICAN JOURNAL OF HUMAN GENETICS
    20. Kohl, S; Baumann, B; Broghammer, M; Jagle, H; Sieving, P; Kellner, U; Spegal, R; Anastasi, M; Zrenner, E; Sharpe, LT; Wissinger, B
      Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21

      HUMAN MOLECULAR GENETICS
    21. Konig, HH; Barry, JC; Leidl, R; Zrenner, E
      Test-effectiveness of orthoptic mass screening in kindergarten for early detection of visual development disorders

      GESUNDHEITSWESEN
    22. Erb, C; Teistler, F; Kohler, K; Guenther, E; Zrenner, E; Thiel, HJ
      Evaluation of the applanation tonometer ProTon in rabbits

      OPHTHALMOLOGE
    23. Besch, D; Wissinger, B; Zrenner, E; Leo-Kottler, B
      A case of liver optic neuropathy with a new point mutation in the cytochrome b gene

      OPHTHALMOLOGE
    24. Jacobi, FK; Broghammer, M; Pesch, K; Zrenner, E; Berger, W; Meindl, A; Pusch, CM
      Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1

      HUMAN GENETICS
    25. Wilhelm, H; Neitzel, J; Wilhelm, B; Beuel, S; Ludtke, H; Kretschmann, U; Zrenner, E
      Pupil perimetry using M-sequence stimulation technique

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    26. Thompson, DA; Gyurus, P; Fleischer, LL; Bingham, EL; McHenry, CL; Apfelstedt-Sylla, E; Zrenner, E; Lorenz, B; Richards, JE; Jacobson, SG; Sieving, PA; Gal, A
      Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    27. Kurtenbach, A; Langrova, H; Zrenner, E
      Multifocal oscillatory potentials in type 1 diabetes without retinopathy

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    28. Werner, A; Sharpe, LT; Zrenner, E
      Asymmetries in the time-course of chromatic adaptation and the significance of contrast

      VISION RESEARCH
    29. Scholl, HPN; Kremers, J; Apfelstedt-Sylla, E; Zrenner, E
      L- and M-cone driven ERGs are differently altered in Best's macular dystrophy

      VISION RESEARCH
    30. Stett, A; Barth, W; Weiss, S; Haemmerle, H; Zrenner, E
      Electrical multisite stimulation of the isolated chicken retina

      VISION RESEARCH
    31. Scholl, HPN; Zrenner, E
      Electrophysiology in the investigation of acquired retinal disorders

      SURVEY OF OPHTHALMOLOGY
    32. Jahn, R; Bock, A; Breiner, KM; Breunig, KD; Bujard, H; Campos-Ortega, J; Ganten, D; Grummt, I; Gruss, P; Goridis, C; Huber, R; Hoch, M; Jackle, H; Kahmann, R; Koch-Brandt, C; Leptin, M; Michel, H; Noegel, A; Neher, E; Nusslein-Volhard, C; Pfanner, N; Sandhoff, K; Schoen, A; Schwille, P; Simons, K; Zrenner, E
      Distinguished scientists back Germany's DFG . . .

      NATURE
    33. Bauer, A; Kolling, G; Dietz, K; Zrenner, E; Schiefer, U
      Are squinters second-class motorists? Influence of stereoscopic disparity on driving performance

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    34. Sobottka, B; Schlote, T; Besch, D; Djelebova, T; Wilhelm, H; Zrenner, E
      Cancer-associated retinopathy - A review article with some clinical examples

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    35. Janecke, AR; Meins, M; Sadeghi, M; Grundmann, K; Apfelstedt-Sylla, E; Zrenner, E; Rosenberg, T; Gal, A
      Twelve novel myosin VIIA mutations in 34 patients with Usher syndrome typeI: Confirmation of genetic heterogeneity

      HUMAN MUTATION
    36. Hettesheimer, H; Erb, C; Schiefer, U; Zrenner, E
      White-noise field campimetry in patients with HIV infection

      OPHTHALMOLOGE
    37. Besch, D; Leo-Kottler, B; Zrenner, E; Wissinger, B
      Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    38. Kurtenbach, A; Neu, A; Zrenner, E
      A temporal deficit in juvenile diabetics

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    39. Erb, C; Nicaeus, T; Adler, M; Isensee, J; Zrenner, E; Thiel, HJ
      Colour vision disturbances in chronic smokers

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    40. Kretschmann, U; Stilling, R; Ruther, K; Zrenner, E
      Familial macular cone dystrophy: diagnostic value of multifocal ERG and two-color threshold perimetry

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    41. Seeliger, M; Pfister, M; Gendo, K; Paasch, S; Apfelstedt-Sylla, E; Plinkert, P; Zenner, HP; Zrenner, E
      Comparative study of visual, auditory, and olfactory function in Usher syndrome

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    42. Friedburg, C; Serey, L; Sharpe, LT; Trauzettel-Klosinski, S; Zrenner, E
      Evaluation of the Night Vision Spectacles on patients with impaired night vision

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    43. Erb, C; Ulrich, A; Adler, M; Flammer, J; Zrenner, E
      Influence of illumination on results of the hue-discrimination test, Roth 28-Hue desaturated

      NEURO-OPHTHALMOLOGY
    44. Wolf, S; Sharpe, LT; Schmidt, HJA; Knau, H; Weitz, S; Kioschis, P; Poustka, A; Zrenner, E; Lichter, P; Wissinger, B
      Direct visual resolution of gene copy number in the human photopigment gene array

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    45. Seeliger, MW; Biesalski, HK; Wissinger, B; Gollnick, H; Gielen, S; Frank, J; Beck, S; Zrenner, E
      Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesis

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    46. Zrenner, E
      No cause for alarm over retinal side-effects of sildenafil

      LANCET
    47. Kurtenbach, A; Schiefer, U; Neu, A; Zrenner, E
      Development of brightness matching and colour vision deficits in juvenile diabetics

      VISION RESEARCH
    48. Guenther, E; Troger, B; Schlosshauer, B; Zrenner, E
      Long-term survival of retinal cell cultures on retinal implant materials

      VISION RESEARCH
    49. Tornow, RP; Stilling, R; Zrenner, E
      Scanning laser densitometry and color perimetry demonstrate reduced photopigment density and sensitivity in two patients with retinal degeneration

      VISION RESEARCH
    50. Baehr, W; Spekreijse, H; Zrenner, E
      Retinal development, degeneration and functional restitution

      VISION RESEARCH
    51. Guenther, E; Schmid, S; Reiff, D; Zrenner, E
      Maturation of intrinsic membrane properties in rat retinal ganglion cells

      VISION RESEARCH
    52. Zrenner, E; Stett, A; Weiss, S; Aramant, RB; Guenther, E; Kohler, K; Miliczek, KD; Seiler, MJ; Haemmerle, H
      Can subretinal microphotodiodes successfully replace degenerated photoreceptors?

      VISION RESEARCH
    53. Eckstein, A; Zrenner, E
      Hepatic retinopathia: changes in retinal function - Reply

      VISION RESEARCH
    54. Zrenner, E; Gabel, VP; Haemmerle, H; Hoefflinger, B; Schubert, M
      Reply to the letter of Drs. Chow and Peachey: The subretinal microphotodiode array retinal prosthesis II

      OPHTHALMIC RESEARCH
    55. Biel, M; Seeliger, M; Pfeifer, A; Kohler, K; Gerstner, A; Ludwig, A; Jaissle, G; Fauser, S; Zrenner, E; Hofmann, F
      Selective loss of cone function in mice lacking the cyclic nucleotide-gated channel CNG3

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    56. Schaeffel, F; Zrenner, E
      Myopia caused in infants and young Children by night-time light in the sleeping room?

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    57. Heine, S; Ruther, K; Isensee, J; Zrenner, E
      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 relevance

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    58. Marmor, MF; Zrenner, E
      Standard for clinical electroretinography (1999 update)

      DOCUMENTA OPHTHALMOLOGICA
    59. Kurtenbach, A; Schiefer, U; Neu, A; Zrenner, E
      Preretinopic changes in the colour vision of juvenile diabetics

      BRITISH JOURNAL OF OPHTHALMOLOGY
    60. Biesalski, HK; Frank, J; Beck, SC; Heinrich, F; Illek, B; Reifen, R; Gollnick, H; Seeliger, MW; Wissinger, B; Zrenner, E
      Biochemical but not clinical vitamin A deficiency results from mutations in the gene for retinol binding protein

      AMERICAN JOURNAL OF CLINICAL NUTRITION
    61. KOHL S; MARX T; GIDDINGS I; JAGLE H; JACOBSON SG; APFELSTEDTSYLLA E; ZRENNER E; SHARPE LT; WISSINGER B
      TOTAL COLOURBLINDNESS IS CAUSED BY MUTATIONS IN THE GENE ENCODING THEALPHA-SUBUNIT OF THE CONE PHOTORECEPTOR CGMP-GATED CATION CHANNEL

      Nature genetics
    62. 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
      AN L-TYPE CALCIUM-CHANNEL GENE MUTATED IN INCOMPLETE X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS

      Nature genetics
    63. LEOKOTTLER B; CHRISTADLER M; WISSINGER B; ZRENNER E
      MISDIAGNOSIS OF LEBERS HEREDITARY OPTIC NEUROPATHY (LHON) - ROLE OF CLINICAL AND MOLECULAR-GENETIC EXAMINATIONS

      Der Ophthalmologe
    64. FRANK J; BECK SC; SEELIGER M; WISSINGER M; ZRENNER E; BIESALSKI HK
      BIOCHEMICAL VITAMIN-A-DEFICIENCY AS A RESULT OF A MUTATION OF THE RBPGENE

      The FASEB journal
    65. WISSINGER B; JAGLE H; KOHL S; BROGHAMMER M; BAUMANN B; HANNA DB; HEDELS C; APFELSTEDTSYLLA E; RANDAZZO G; JACOBSON SG; ZRENNER E; SHARPE LT
      HUMAN ROD MONOCHROMACY - LINKAGE ANALYSIS AND MAPPING OF A CONE PHOTORECEPTOR EXPRESSED CANDIDATE GENE ON CHROMOSOME 2Q11

      Genomics (San Diego, Calif.)
    66. LEOKOTTLER B; KLEIN R; BERG PA; ZRENNER E
      OCULAR SYMPTOMS IN ASSOCIATION WITH ANTIPHOSPHOLIPID ANTIBODIES

      Graefe's archive for clinical and experimental ophthalmology
    67. RUTHER K; EHLICH P; PHILIPP A; ECKSTEIN A; ZRENNER E
      PROGNOSTIC VALUE OF THE PATTERN ELECTRORETINOGRAM IN CASES OF TUMORS AFFECTING THE OPTIC PATHWAY

      Graefe's archive for clinical and experimental ophthalmology
    68. FRIEDBURG C; SHARPE LT; BEUEL S; ZRENNER E
      A COMPUTER-CONTROLLED SYSTEM FOR MEASURING DARK-ADAPTATION AND OTHER PSYCHOPHYSICAL FUNCTIONS

      Graefe's archive for clinical and experimental ophthalmology
    69. SEELIGER MW; KRETSCHMANN UH; APFELSTEDTSYLLA E; ZRENNER E
      IMPLICIT TIME TOPOGRAPHY OF MULTIFOCAL ELECTRORETINOGRAMS

      Investigative ophthalmology & visual science
    70. KRETSCHMANN U; SEELIGER M; RUETHER K; USUI T; ZRENNER E
      SPATIAL CONE ACTIVITY DISTRIBUTION IN DISEASES OF THE POSTERIOR POLE DETERMINED BY MULTIFOCAL ELECTRORETINOGRAPHY

      Vision research (Oxford)
    71. MOLLON JD; CAVONIUS CR; ZRENNER E
      PROCEEDINGS OF THE INTERNATIONAL-COLOR-VISION SOCIETY - FOREWORD

      Vision research (Oxford)
    72. USUI T; KREMERS J; SHARPE LT; ZRENNER E
      RESPONSE PHASE OF THE FLICKER ELECTRORETINOGRAM (ERG) IS INFLUENCED BY CONE EXCITATION STRENGTH

      Vision research (Oxford)
    73. USUI T; KREMERS J; SHARPE LT; ZRENNER E
      FLICKER CONE ELECTRORETINOGRAM IN DICHROMATS AND TRICHROMATS

      Vision research (Oxford)
    74. ERB C; ADLER M; STUBIGER N; WOHLRAB M; ZRENNER E; THIEL HJ
      COLOR-VISION IN NORMAL SUBJECTS TESTED BY THE COLOR ARRANGEMENT TEST ROTH 28-HUE DESATURATED

      Vision research (Oxford)
    75. KRETSCHMANN U; TORNOW RP; ZRENNER E
      MULTIFOCAL ERG REVEALS LONG-DISTANCE EFFECTS OF A LOCAL BLEACH IN THERETINA

      Vision research (Oxford)
    76. ZRENNER E; GABEL VP; HAEMMERLE H; HOEFFLINGER B; SCHUBERT M
      SUBRETINAL IMPLANTS

      Ophthalmic research
    77. ZRENNER E
      HOW TO EVALUATE VISUAL DISORDERS ASSOCIATED WITH VIAGRA, ESPECIALLY RETINAL DEGENERATION

      Klinische Monatsblatter fur Augenheilkunde
    78. KRETSCHMANN U; SCHLOTE T; STUBIGER N; GENDO K; HIPP E; ZRENNER E
      MULTIFOCAL ELECTRORETINOGRAPHY IN MACULAR DISEASES

      Klinische Monatsblatter fur Augenheilkunde
    79. KRETSCHMANN U; GENDO K; WILHELM H; SCHIEFER U; HETTESHEIMER H; ZRENNER E
      OBJECTIVE ASSESSMENT OF VISUAL-FIELD DEFE CTS BY MULTIFOCAL ERG

      Klinische Monatsblatter fur Augenheilkunde
    80. KRETSCHMANN U; SEELIGER MW; RUETHER K; USUI T; APFELSTEDTSYLLA E; ZRENNER E
      MULTIFOCAL ELECTRORETINOGRAPHY IN PATIENTS WITH STARGARDTS-MACULAR-DYSTROPHY

      British journal of ophthalmology
    81. SEELIGER M; KRETSCHMANN U; APFELSTEDTSYLLA E; RUTHER K; ZRENNER E
      MULTIFOCAL ELECTRORETINOGRAPHY IN RETINITIS-PIGMENTOSA

      American journal of ophthalmology
    82. Zrenner, E; Lutjen-Drecoll, E
      Hereditary retinal degeneration - Preface

      ACTA ANATOMICA
    83. Kohl, S; Giddings, I; Besch, D; Apfelstedt-Sylla, E; Zrenner, E; Wissinger, B
      The role of the peripherin/RDS gene in retinal dystrophies

      ACTA ANATOMICA
    84. GAL A; APFELSTEDTSYLLA E; JANECKE AR; ZRENNER E
      RHODOPSIN MUTATIONS IN INHERITED RETINAL DYSTROPHIES AND DYSFUNCTIONS

      Progress in retinal and eye research
    85. MARLHENS F; BAREIL C; GRIFFOIN JM; ZRENNER E; AMALRIC P; ELIAOU C; LIU SY; HARRIS E; REDMOND TM; ARNAUD B; CLAUSTRES M; HAMEL CP
      MUTATIONS IN RPE65 CAUSE LEBERS CONGENITAL AMAUROSIS

      Nature genetics
    86. 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
      MOUSE CHOROIDEREMIA GENE MUTATION CAUSES PHOTORECEPTOR CELL DEGENERATION AND IS NOT TRANSMITTED THROUGH THE FEMALE GERMLINE

      Human molecular genetics
    87. WISSINGER B; MULLER F; WEYAND I; SCHUFFENHAUER S; THANOS S; KAUPP UB; ZRENNER E
      CLONING, CHROMOSOMAL LOCALIZATION AND FUNCTIONAL EXPRESSION OF THE GENE ENCODING THE ALPHA-SUBUNIT OF THE CGMP-GATED CHANNEL IN HUMAN CONE PHOTORECEPTORS

      European journal of neuroscience
    88. KOHLER K; WHEELERSCHILLING T; JURKLIES B; GUENTHER E; ZRENNER E
      ANGIOTENSIN-II IN THE RABBIT RETINA

      Visual neuroscience
    89. SEELINGER M; RUTHER K; APFELSTEDTSYLLA E; SCHLOTE W; WOHLRAB M; ZRENNER E
      DIAGNOSTIC PROCEDURES AND OPHTHALMOLOGIC FINDINGS IN JUVENILE NEURONAL CEROID-LIPOFUSCINOSIS (BATTEN-MAYOU)

      Der Ophthalmologe
    90. EHLICH P; SADOWSKI B; ZRENNER E
      OLIGOCONE TRICHROMASY - A RARE FORM OF IN COMPLETE MONOCHROMATISM

      Der Ophthalmologe
    91. KRETSCHMANN U; USUI T; RUETHER K; ZRENNER E
      ELECTRORETINOGRAPHIC CAMPIMETRY IN A PATIENT WITH CRYSTALLINE RETINOPATHY

      German journal of ophthalmology
    92. CREMERS FPM; VANDENHURK JAJM; HENDRIKS W; VANDEPOL TJR; OERLEMANS F; JAISSLE G; KOHLER K; RUTHER K; HARTMANN J; ZRENNER E; WIERINGA B; ROPERS HH
      THE CHOROIDEREMIA MUTATION RESULTS IN PHOTORECEPTOR CELL DEGENERATIONIN CHIMERIC MICE BUT IS EMBRYONIC LETHAL IN HEMIZYGOTIC MICE

      The FASEB journal
    93. KREMMER S; ECKSTEIN A; GAL A; APFELSTEDTSYLLA E; WEDEMANN H; RUTHER K; ZRENNER E
      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
    94. GUENTHER E; HEWIG B; ZRENNER E; KOHLER K
      ANGIOTENSIN-II-INDUCED INHIBITION AND FACILITATION OF CALCIUM CURRENTSUBTYPES IN RAT RETINAL GANGLION-CELLS

      Neuroscience letters
    95. KOHLER K; LILIENTHAL H; GUENTHER E; WINNEKE G; ZRENNER E
      PERSISTENT DECREASE OF THE DOPAMINE-SYNTHESIZING ENZYME TYROSINE-HYDROXYLASE IN THE RHESUS-MONKEY RETINA AFTER CHRONIC LEAD-EXPOSURE

      Neurotoxicology
    96. FELBOR U; DOEPNER D; SCHNEIDER U; ZRENNER E; WEBER BHF
      EVALUATION OF THE GENE ENCODING THE TISSUE INHIBITOR OF METALLOPROTEINASES-3 IN VARIOUS MACULOPATHIES

      Investigative ophthalmology & visual science
    97. SCHWAHN HN; SCHAEFFEL F; ZRENNER E
      EFFECTS OF ATROPINE IN THE CHICKEN RETINA - IN-VITRO STUDIES ON A RETINA-RPE-CHOROID PREPARATION

      Investigative ophthalmology & visual science
    98. BESCH D; CHRISTADLER M; LEOKOTTLER B; ZRENNER E; WISSINGER B
      SCREEN FOR MUTATIONS OF THE MITOCHONDRIAL-DNA IN PATIENTS WITH LEBERS-HEREDITARY-OPTIC-NEUROPATHY (LHON)

      Investigative ophthalmology & visual science
    99. APFELSTEDTSYLLA E; MEITINGER T; MEINDL A; HERMANN K; BRANDAU O; WISSINGER B; ENGEL C; ZRENNER E
      RPGR MISSENSE MUTATION IN CONGENITAL STATIONARY NIGHT BLINDNESS (CSNB)

      Investigative ophthalmology & visual science
    100. FRIEDBURG C; SEREY L; SHARPE LT; TRAUZETTELKLOSINSKI S; ZRENNER E
      EVALUATION OF THE NIGHT-VISION SYSTEM (NIVIS)

      Investigative ophthalmology & visual science


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/10/20 alle ore 16:42:48