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La ricerca find articoli where soggetti phrase all words 'RETINOSCHISIS' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 80 riferimenti
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    1. Hiraoka, M; Rossi, F; Trese, MT; Shastry, BS
      X-linked juvenile retinoschisis: mutations at the retinoschisis and Norriedisease gene loci?

      JOURNAL OF HUMAN GENETICS
    2. Bringmann, A; Reichenbach, A
      Role of Muller cells in retinal degenerations

      FRONTIERS IN BIOSCIENCE
    3. Alexander, KR; Barnes, CS; Fishman, GA
      Origin of deficits in the flicker electroretinogram of the cone system in X-linked retinoschisis as derived from response nonlinearities

      JOURNAL OF THE OPTICAL SOCIETY OF AMERICA A-OPTICS IMAGE SCIENCE AND VISION
    4. Jurklies, B; Weismann, M; Kellner, U; Zrenner, E; Bornfeld, N
      Clinical findings in autosomal recessive enhanced S-cone sensitivity syndrome

      OPHTHALMOLOGE
    5. Isola, V; Spinelli, G; Misefari, W
      Transpupillary retinopexy of chorioretinal lesions predisposing to retinaldetachment with the use of diode (810 nm) microlaser

      RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
    6. McKibbin, M; Booth, AP; George, NDL
      Foveal ectopia in X-linked retinoschisis

      RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES
    7. Alexander, KR; Barnes, CS; Fishman, GA
      High-frequency attenuation of the cone ERG and ON-response deficits in X-linked retinoschisis

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    8. Molday, LL; Hicks, D; Sauer, CG; Weber, BHF; Molday, RS
      Expression of X-linked retinoschisis protein RS1 in photoreceptor and bipolar cells

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    9. Alexander, KR; Fishman, GA; Barnes, CS; Grover, S
      ON-response deficit in the electroretinogram of the cone system in X-linked retinoschisis

      INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE
    10. Berinstein, DM; Hiraoka, M; Trese, MT; Shastry, BS
      Coats' disease and congenital retinoschisis in a single eye: A case reportand DNA analysis

      OPHTHALMOLOGICA
    11. Mielke, J; Freudenthaler, N; Schlote, T; Bartz-Schmidt, KU
      Pseudohypopyon of cholesterol crystals occurring 16 years after retinal detachment in x-linked retinoschisis

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    12. Curat, CA; Eck, M; Dervillez, X; Vogel, WF
      Mapping of epitopes in discoidin domain receptor 1 critical for collagen binding

      JOURNAL OF BIOLOGICAL CHEMISTRY
    13. Imai, M; Iijima, H; Hanada, N
      Optical coherence tomography of tractional macular elevations in eyes withproliferative diabetic retinopathy (vol 132, pg 81, 2001)

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    14. Imai, M; Iijima, H; Hanada, N
      Optical coherence tomography of tractional macular elevations in eyes withproliferative diabetic retinopathy

      AMERICAN JOURNAL OF OPHTHALMOLOGY
    15. Huopaniemi, L; Tyynismaa, H; Rantala, A; Rosenberg, T; Alitalo, T
      Characterization of two unusual RS1 gene deletions segregating in Danish retinoschisis families

      HUMAN MUTATION
    16. Hrynchak, P; Simpson, T
      Optical coherence tomography: An introduction to the technique and its use

      OPTOMETRY AND VISION SCIENCE
    17. Grayson, C; Reid, SNM; Ellis, JA; Rutherford, A; Sowden, JC; Yates, JRW; Farber, DB; Trump, D
      Retinoschisin, the X-linked retinoschisis protein, is a secreted photoreceptor protein, and is expressed and released by Weri-Rb1 cells

      HUMAN MOLECULAR GENETICS
    18. Livesey, FJ; Furukawa, T; Steffen, MA; Church, GM; Cepko, CL
      Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx

      CURRENT BIOLOGY
    19. Ando, A; Takahashi, K; Sho, K; Matsushima, M; Okamura, A; Uyama, M
      Histopathological findings of X-linked retinoschisis with neovascular glaucoma

      GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
    20. Hamel, CP; Griffoin, JM; Bazalgette, C; Lasquellec, L; Duval, PA; Bareil, C; Beaufrere, L; Bonnet, S; Eliaou, C; Marlhens, F; Schmitt-Bernard, CF; Tuffery, S; Claustres, M; Arnaud, B
      Molecular genetics of pigmentary retinopathies: Identification of mutations in CHM, RDS, RHO, RPE65, USH2A and XLRS1 genes

      JOURNAL FRANCAIS D OPHTALMOLOGIE
    21. Alexander, KR; Fishman, GA; Grover, S
      Temporal frequency deficits in the electroretinogram of the cone system inX-linked retinoschisis

      VISION RESEARCH
    22. Shastry, BS; Hiraoka, M; Trese, MT
      Lack of association of the Norrie disease gene with retinoschisis phenotype

      JAPANESE JOURNAL OF OPHTHALMOLOGY
    23. Vrabec, TR
      Pneumatic retinopexy in a progressive rhegmatogenous retinoschisis retinaldetachment

      ARCHIVES OF OPHTHALMOLOGY
    24. Inoue, Y; Yamamoto, S; Okada, M; Tsujikawa, M; Inoue, T; Okada, AA; Kusaka, S; Saito, Y; Wakabayashi, K; Miyake, Y; Fujikado, T; Tano, Y
      X-linked retinoschisis with point mutations in the XLRS1 gene

      ARCHIVES OF OPHTHALMOLOGY
    25. Ikaheimo, K; Tuppurainen, K; Mantyjarvi, M
      Clinical features of Goldmann-Favre syndrome

      ACTA OPHTHALMOLOGICA SCANDINAVICA
    26. Lesnoni, G; Rossi, T; Nistri, A; Boccassini, B
      Nanophthalmic uveal effusion syndrome after prophylactic laser treatment

      EUROPEAN JOURNAL OF OPHTHALMOLOGY
    27. Hiriyanna, KT; Bingham, EL; Yashar, BM; Ayyagari, R; Fishman, G; Small, KW; Weinberg, DV; Weleber, RG; Lewis, RA; Andreasson, S; Richards, JE; Sieving, PA
      Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change

      HUMAN MUTATION
    28. Huopaniemi, L; Rantala, A; Forsius, H; Somer, M; de la Chapelle, A; Alitalo, T
      Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland

      EUROPEAN JOURNAL OF HUMAN GENETICS
    29. Meier, P; Wiedemann, P
      Vitreoretinal surgery in children

      OPHTHALMOLOGE
    30. Clemens, S
      Senile retinoschisis and schisisamotio. Pathogenesis, diagnosis, therapy

      OPHTHALMOLOGE
    31. Walpole, SM; Hiriyana, KT; Nicolaou, A; Bingham, EL; Durham, J; Vaudin, M; Ross, MT; Yates, JRW; Sieving, PA; Trump, D
      Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid induced gene in Xp22

      GENOMICS
    32. Lateef, SS; Mukherji, SK; Castillo, M; Wallace, DK
      Juvenile retinoschisis: Imaging findings

      AMERICAN JOURNAL OF NEURORADIOLOGY
    33. Kelly, J; Maumenee, IH
      Hereditary macular diseases

      INTERNATIONAL OPHTHALMOLOGY CLINICS
    34. Bradshaw, K; George, N; Moore, A; Trump, D
      Mutations of the XLRS1 gene cause abnormalities of photoreceptor as well as inner retinal responses of the ERG

      DOCUMENTA OPHTHALMOLOGICA
    35. Gehrig, A; White, K; Lorenz, B; Andrassi, M; Clemens, S; Weber, BHF
      Assessment of RS1 in X-linked juvenile retinoschisis and sporadic senile retinoschisis

      CLINICAL GENETICS
    36. Shastry, BS; Hejtmancik, FJ; Trese, MT
      Recurrent missense (R197C) and nonsense (Y89X) mutations in the XLRS1 genein families with X-linked retinoschisis

      BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
    37. Huopaniemi, L; Fellman, J; Rantala, A; Eriksson, A; Forsius, H; De la Chapelle, A; Alitalo, T
      Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 gene

      ANNALS OF HUMAN GENETICS
    38. KELLNER U; JANDECK C; KRAUS H; FOERSTER MH
      HEREDITARY MACULAR DYSTROPHIES

      Der Ophthalmologe
    39. MONTINI E; ANDOLFI G; CARUSO A; BUCHNER G; WALPOLE SM; MARIANI M; CONSALEZ GG; TRUMP D; BALLABIO A; FRANCO B
      IDENTIFICATION AND CHARACTERIZATION OF A NOVEL SERINE-THREONINE KINASE GENE FROM THE XP22 REGION

      Genomics (San Diego, Calif.)
    40. VANDEVOSSE E; WALPOLE SM; NICOLAOU A; VANDERBENT P; CAHN A; VAUDIN M; ROSS MT; DURHAM J; PAVITT R; WILKINSON J; GRAFHAM D; BERGEN AAB; VANOMMEN GJB; YATES JRW; DENDUNNEN JT; TRUMP D
      CHARACTERIZATION OF SCML1, A NEW GENE IN XP22, WITH HOMOLOGY TO DEVELOPMENTAL POLYCOMB GENES

      Genomics
    41. RODRIGUEZ IR; MAZURUK K; JAWORSKI C; IWATA F; MOREIRA EF; KAISERKUPFER MI
      NOVEL MUTATIONS IN THE XLRS1 GENE MAY BE CAUSED BY EARLY OKAZAKI FRAGMENT SEQUENCE REPLACEMENT

      Investigative ophthalmology & visual science
    42. OHGURO H; SUZUKI J; NAKAGAWA T
      A CASE OF A COMBINATION OF OGUCHIS-DISEASE AND CONGENITAL RETINOSCHISIS

      Ophthalmologica
    43. DELACHAPELLE A; WRIGHT FA
      LINKAGE DISEQUILIBRIUM MAPPING IN ISOLATED POPULATIONS - THE EXAMPLE OF FINLAND REVISITED

      Proceedings of the National Academy of Sciences of the United Statesof America
    44. FONG DS; FREDERICK AR; BLUMENKRANZ MS; WALTON DS
      EXUDATIVE RETINAL-DETACHMENT IN X-LINKED RETINOSCHISIS

      Ophthalmic surgery
    45. ROSENFELD PJ; FLYNN HW; MCDONALD HR; RUBSAMEN PE; SMIDDY WE; SIPPERLEY JO; BONIUK I; PACKER AJ
      OUTCOMES OF VITREORETINAL SURGERY IN PATIENTS WITH X-LINKED RETINOSCHISIS

      Ophthalmic surgery
    46. ASLAN O; BATMAN C; CEKIC O; OZALP S
      THE USE OF PERFLUORODECALIN IN RETINAL DETACHMENTS WITH RETINOSCHISIS

      Ophthalmic surgery
    47. ROESCH MT; EWING CC; GIBSON AE; WEBER BHF
      THE NATURAL-HISTORY OF X-LINKED RETINOSCHISIS

      Canadian journal of ophthalmology
    48. TANNA AP; ASRANI S; ZEIMER R; ZOU SZ; GOLDBERG MF
      OPTICAL CROSS-SECTIONAL IMAGING OF THE MACULA WITH THE RETINAL THICKNESS ANALYZER IN X-LINKED RETINOSCHISIS

      Archives of ophthalmology
    49. Weber, BHF
      Recent advances in the molecular genetics of hereditary retinal dystrophies with primary involvement of the macula

      ACTA ANATOMICA
    50. WALPOLE SM; NICOLAOU A; HOWELL GR; WHITTAKER A; BENTLEY DR; ROSS MT; YATES JRW; TRUMP D
      HIGH-RESOLUTION PHYSICAL MAP OF THE X-LINKED RETINOSCHISIS INTERVAL IN XP22

      Genomics
    51. RUETHER K; VANDEPOL D; JAISSLE G; BERGER W; TORNOW RP; ZRENNER E
      RETINOSCHISISLIKE ALTERATIONS IN THE MOUSE EYE CAUSED BY GENE TARGETING OF THE NORRIE DISEASE GENE

      Investigative ophthalmology & visual science
    52. ROHRBACH JM; BENZ D; FRIEDRICHS W; THIEL HJ; WEHNER HD
      OCULAR PATHOLOGY OF THE BATTERED-CHILD SY NDROME

      Klinische Monatsblatter fur Augenheilkunde
    53. SHASTRY BS; HEJTMANCIK JF; RODRIGUEZ A; RODRIGUEZ F; TAMAYO ML
      LINKAGE MAPPING OF A LARGE COLOMBIAN FAMILY SEGREGATING FOR X-LINKED RETINOSCHISIS - REFINEMENT OF THE CHROMOSOMAL LOCATION

      Journal of Medical Genetics
    54. BOUCHER MC
      SPONTANEOUS REGRESSION OF JUVENILE RETINOSCHISIS

      Canadian journal of ophthalmology
    55. POLK TD; GASS JDM; GREEN WR; NOVAK MA; JOHNSON MW
      FAMILIAL INTERNAL LIMITING MEMBRANE DYSTROPHY - A NEW SHEEN RETINAL DYSTROPHY

      Archives of ophthalmology
    56. FERRONE PJ; TRESE MT; LEWIS HL
      VITREORETINAL SURGERY FOR COMPLICATIONS OF CONGENITAL RETINOSCHISIS

      American journal of ophthalmology
    57. MARREN SE
      IDIOPATHIC PERIPHERAL VITREOUS MEMBRANES

      Optometry and vision science
    58. VANDEVOSSE E; BERGEN AAB; MEERSHOEK EJ; OOSTERWIJK JC; GREGORY S; BAKKER B; WEISSENBACH J; COFFEY AJ; VANOMMEN GJB; DENDUNNEN JT
      AN XP22.1-P22.2 YAC CONTIG ENCOMPASSING THE DISEASE LOCI FOR RS, KFSD, CLS, HYP AND RP15 - REFINED LOCALIZATION OF RS

      European journal of human genetics
    59. MOORE AT; EVANS K
      MOLECULAR-GENETICS OF CENTRAL RETINAL DYSTROPHIES

      Australian and New Zealand journal of ophthalmology
    60. HOERAUF H; SCHMIDTERFURTH U; LAQUA H
      CLINICAL FINDINGS AFTER VITRECTOMY FOR RE TINAL-DETACHMENT ASSOCIATEDWITH AN OPTIC DISC PIT

      Klinische Monatsblatter fur Augenheilkunde
    61. GEORGE NDL; PAYNE SJ; BILL RM; BARTON DE; MOORE AT; YATES JRW
      IMPROVED GENETIC-MAPPING OF X-LINKED RETINOSCHISIS

      Journal of Medical Genetics
    62. LOMEO MD; DIAZROHENA R; LAMBERT HM
      USE OF PERFLUOROCARBON LIQUID IN THE REPAIR OF RETINOSCHISIS RETINAL DETACHMENTS

      Ophthalmic surgery
    63. KIRSCH LS; BROWNSTEIN S; DEWOLFFROUENDAAL D
      A HISTOPATHOLOGICAL, ULTRASTRUCTURAL AND IMMUNOHISTOCHEMICAL STUDY OFCONGENITAL HEREDITARY RETINOSCHISIS

      Canadian journal of ophthalmology
    64. GEORGE NDL; YATES JRW; MOORE AT
      CLINICAL-FEATURES IN AFFECTED MALES WITH X-LINKED RETINOSCHISIS

      Archives of ophthalmology
    65. PAWAR H; BINGHAM EL; HIRIYANNA K; SEGAL M; RICHARDS JE; SIEVING PA
      X-LINKED JUVENILE RETINOSCHISIS - LOCALIZATION BETWEEN (DXS1195, DXS418) AND AFM291WF5 ON A SINGLE YAC

      Human heredity
    66. ALITALO T; FRANCIS F; KERE J; LEHRACH H; SCHLESSINGER D; WILLARD HF
      A 6-MB YAC CONTIG IN XP22.1 SPANNING THE DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3, AND PHKA2 GENES

      Genomics
    67. MADJAROV B; HILTON GF; BRINTON DA; LEE SS
      A NEW CLASSIFICATION OF THE RETINOSCHISES

      Retina
    68. PELTONEN L; PEKKARINEN P; AALTONEN J
      MESSAGES FROM AN ISOLATE - LESSONS FROM THE FINNISH GENE POOL

      Biological chemistry Hoppe-Seyler
    69. CLEMENS S; BUSSE H; GERDING H; HOFFMANN P
      TREATMENT GUIDELINES IN DIFFERENT STAGES OF SENILE RETINOSCHISIS

      Klinische Monatsblatter fur Augenheilkunde
    70. GEORGE NDL; YATES JRW; BRADSHAW K; MOORE AT
      INFANTILE PRESENTATION OF X-LINKED RETINOSCHISIS

      British journal of ophthalmology
    71. GEORGE NDL; YATES JRW; MOORE AT
      X-LINKED RETINOSCHISIS

      British journal of ophthalmology
    72. PAWAR H; BINGHAM EL; LUNETTA KL; SEGAL M; RICHARDS JE; BOEHNKE M; SIEVING PA
      REFINED GENETIC-MAPPING OF JUVENILE X-LINKED RETINOSCHISIS

      Human heredity
    73. BIANCALANA V; TRIVIER E; WEBER C; WEISSENBACH J; ROWE PSN; ORIORDAN JLH; PARTINGTON MW; HEYBERGER S; OUDET C; HANAUER A
      CONSTRUCTION OF A HIGH-RESOLUTION LINKAGE MAP FOR XP22.1-P22.2 AND REFINEMENT OF THE GENETIC LOCALIZATION OF THE COFFIN-LOWRY SYNDROME GENE

      Genomics
    74. FALSINI B; IAROSSI G; PORCIATTI V; MERENDINO E; FADDA A; CERMOLA S; BUZZONETTI L
      POSTRECEPTORAL CONTRIBUTION TO MACULAR DYSFUNCTION IN RETINITIS-PIGMENTOSA

      Investigative ophthalmology & visual science
    75. KELLNER U; ZRENNER E; SADOWSKI B; FOERSTER MH
      ENHANCED S-CONE SENSITIVITY SYNDROME - LONG-TERM FOLLOW-UP, ELECTROPHYSIOLOGICAL AND PSYCHOPHYSICAL FINDINGS

      Clinical vision sciences
    76. LEMRINI F; DAFRALLAH L; KABBAJ A
      RETINAL-DETACHMENT IN CHILDREN

      Journal francais d'ophtalmologie
    77. YEVGRAFOV VY; BALASHOVA LM
      OCULAR CIRCULATION IN RETINAL-DETACHMENT AND SURGICAL-TREATMENT THEREOF

      Vestnik oftal'mologii
    78. ANASTASI M; BRAI M; LAURICELLA M; GERACITANO R
      METHODOLOGICAL ASPECTS OF THE APPLICATION OF THE NAKA-RUSHTON EQUATION TO CLINICAL ELECTRORETINOGRAM

      Ophthalmic research
    79. KELLNER U; FOERSTER MH
      CONE DYSTROPHIES WITH NEGATIVE PHOTOPIC ELECTRORETINOGRAM

      British journal of ophthalmology
    80. RUDANKO SL; FLAGE T; HANSEN E; ROSENBERG T; VIGGOSSON G; RIISE R
      VISUAL IMPAIRMENT IN NORDIC CHILDREN .5. X-LINKED JUVENILE RETINOSCHISIS

      Acta ophthalmologica


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Documento generato il 22/01/21 alle ore 10:11:56