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La ricerca find articoli where soggetti phrase all words 'EXUDATIVE VITREORETINOPATHY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 36 riferimenti
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    1. Haider, MZ; Devarajan, LV; Al-Essa, M; Srivastva, BS; Kumar, H; Azad, R; Rashwan, N
      Retinopathy of prematurity: Mutations in the Norrie disease gene and the risk of progression to advanced stages

      PEDIATRICS INTERNATIONAL
    2. Yamada, K; Limprasert, P; Ratanasukon, M; Tengtrisorn, S; Yingchareonpukdee, J; Vasiknsenonte, P; Kitaoka, T; Ghadami, M; Niikawa, N; Kishino, T
      Two Thai families with Norrie disease (ND): Association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier

      AMERICAN JOURNAL OF MEDICAL GENETICS
    3. Ott, S; Patel, RJ; Apukuttan, B; Wang, XG; Stout, JT
      A novel mutation in the Norrie disease gene

      JOURNAL OF AAPOS
    4. Shastry, BS; Trese, MT
      Evaluation of the Norrie disease gene in a family with Incontinentia pigmenti

      OPHTHALMIC RESEARCH
    5. Meier, P; Wiedemann, P
      Vitreoretinal surgery in children

      OPHTHALMOLOGE
    6. Hartzer, MK; Cheng, M; Liu, X; Shastry, BS
      Localization of the Norrie disease gene mRNA by in situ hybridization

      BRAIN RESEARCH BULLETIN
    7. Rattner, A; Sun, H; Nathans, J
      Molecular genetics of human retinal disease

      ANNUAL REVIEW OF GENETICS
    8. ZAREMBA J; FEIL S; JUSZKO J; MYGA W; VANDUIJNHOVEN G; BERGER W
      INTRAFAMILIAL VARIABILITY OF THE OCULAR PHENOTYPE IN A POLISH FAMILY WITH A MISSENSE MUTATION (A63D) IN THE NORRIE-DISEASE GENE

      Ophthalmic genetics
    9. MACDONALD IM; HANEY PM; MUSARELLA MA
      SUMMARY OF OCULAR GENETIC-DISORDERS AND INHERITED SYSTEMIC CONDITIONSWITH EYE FINDINGS

      Ophthalmic genetics
    10. INGLEHEARN CF
      MOLECULAR-GENETICS OF HUMAN RETINAL DYSTROPHIES

      Eye
    11. RICHTER M; GOTTANKA J; MAY CA; WELGELUSSEN U; BERGER W; LUTJENDRECOLL E
      RETINAL VASCULATURE CHANGES IN NORRIE-DISEASE MICE

      Investigative ophthalmology & visual science
    12. DECRECCHIO G; SIMONELLI F; NUNZIATA G; MAZZEO S; GRECO GM; RINALDI E; VENTRUTO V; CICCODICOLA A; MIANO MG; TESTA F; CURCI A; DURSO M; RINALDI MM; CAVALIERE ML; CASTELLUCCIO P
      AUTOSOMAL RECESSIVE FAMILIAL EXUDATIVE VITREORETINOPATHY - EVIDENCE FOR GENETIC-HETEROGENEITY

      Clinical genetics
    13. Berger, W
      Molecular dissection of Norrie disease

      ACTA ANATOMICA
    14. AZUARABLANCO A; PESIN SR; KATZ LJ; MICHAEL AJ; TASMAN WS
      FAMILIAL EXUDATIVE VITREORETINOPATHY ASSOCIATED WITH NONNEOVASCULAR CHRONIC ANGLE-CLOSURE GLAUCOMA

      Journal of glaucoma
    15. PENDERGAST SD; TRESE MT; SHASTRY BS
      OCULAR FINDINGS IN CUTIS MARMORATA TELANGIECTATICA CONGENITA - BILATERAL EXUDATIVE VITREORETINOPATHY

      Retina
    16. 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
    17. SHASTRY BS; PENDERGAST SD; HARTZER MK; LIU XY; TRESE MT
      IDENTIFICATION OF MISSENSE MUTATIONS IN THE NORRIE DISEASE GENE ASSOCIATED WITH ADVANCED RETINOPATHY OF PREMATURITY

      Archives of ophthalmology
    18. CABALLERO M; VESKE A; RODRIGUEZ JJ; LUGO N; SCHROEDER B; HESSE L; GAL A
      2 NOVEL MUTATIONS IN THE NORRIE DISEASE GENE ASSOCIATED WITH THE CLASSICAL OCULAR PHENOTYPE

      Ophthalmic genetics
    19. PRICE SM; PERIAM N; HUMPHRIES A; WOODRUFF G; TREMBATH RC
      FAMILIAL EXUDATIVE VITREORETINOPATHY LINKED TO D11S533 IN A LARGE ASIAN FAMILY WITH CONSANGUINITY

      Ophthalmic genetics
    20. KELLNER U; FUCHS S; BORNFELD N; FOERSTER MH; GAL A
      OCULAR PHENOTYPES ASSOCIATED WITH 2 MUTATIONS (R121W, C126X) IN THE NORRIE-DISEASE GENE

      Ophthalmic genetics
    21. MARREN SE
      IDIOPATHIC PERIPHERAL VITREOUS MEMBRANES

      Optometry and vision science
    22. BARREAU E; COHEN SY; COSCAS G
      DRAGGED DISC SYNDROME - ETIOLOGIES - A CA SE-REPORT

      Journal francais d'ophtalmologie
    23. TASMAN W
      HISTORY OF RETINA 1896-1996

      Ophthalmology
    24. MINTZHITTNER HA; FERRELL RE; SIMS KB; FERNANDEZ KM; GEMMELL BS; SATRIANO DR; CASTER J; KRETZER FL
      PERIPHERAL RETINOPATHY IN OFFSPRING OF CARRIERS OF NORRIE DISEASE GENE-MUTATIONS - POSSIBLE TRANSPLACENTAL EFFECT OF ABNORMAL NORRIN

      Ophthalmology
    25. JOHNSON K; MINTZHITTNER HA; CONLEY YP; FERRELL RE
      X-LINKED EXUDATIVE VITREORETINOPATHY CAUSED BY AN ARGININE TO LEUCINESUBSTITUTION (R121L) IN THE NORRIE DISEASE PROTEIN

      Clinical genetics
    26. JANDECK C; KELLNER U; KOSSEL H; BARTSCH M; VERSMOLD HT; FOERSTER MH
      RETINOPATHY OF PREMATURITY IN INFANTS OF BIRTH-WEIGHT GREATER-THAN-2000G AFTER HEMORRHAGIC-SHOCK AT BIRTH

      British journal of ophthalmology
    27. CHYNN EW; WALTON DS; HAHN LB; DRYJA TP
      NORRIE DISEASE - DIAGNOSIS OF A SIMPLEX CASE BY DNA ANALYSIS

      Archives of ophthalmology
    28. CHEN ZY; DENNEY RM; BREAKEFIELD XO
      NORRIE DISEASE AND MAO GENES - NEAREST NEIGHBORS

      Human molecular genetics
    29. CLEMENT F; BECKFORD CA; CORRAL A; JIMENEZ R
      X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY - REPORT OF ONE FAMILY

      Retina
    30. KHAIRALLAH M; BELAIBA A; ALOULOU K
      FAMILIAL EXUDATIVE VITREORETINOPATHY AND HEREDITARY RETINAL VASCULAR TORTUOSITY

      Journal francais d'ophtalmologie
    31. SELLER MJ; PAL K; HORSLEY S; DAVIES AF; BERRY AC; MEREDITH R; MCCARTNEY ACE
      A FETUS WITH AN X-1 BALANCED RECIPROCAL TRANSLOCATION AND EYE DISEASE

      Journal of Medical Genetics
    32. MACDONALD IM; SASI R
      MOLECULAR-GENETICS OF INHERITED EYE DISORDERS

      Clinical and investigative medicine
    33. UTO H; SHIGETO M; TANAKA H; UCHIDA H; OHNISHI Y; NISHIMURA M
      A CASE OF 11Q--SYNDROME-ASSOCIATED WITH ABNORMALITIES OF THE RETINAL-VESSELS

      Ophthalmologica
    34. ROSENFELD PJ; MCKUSICK VA; AMBERGER JS; DRYJA TP
      RECENT ADVANCES IN THE GENE MAP OF INHERITED EYE DISORDERS - PRIMARY HEREDITARY-DISEASES OF THE RETINA, CHOROID, AND VITREOUS

      Journal of Medical Genetics
    35. MACDONALD IM
      RECENT ADVANCES IN THE MOLECULAR-GENETICS OF INHERITED EYE DISORDERS

      Canadian journal of ophthalmology
    36. SCHMIDT D; SORIANO JM
      RETINAL TELANGIECTASIS AND PROLIFERATION OF THE RETINAL-VESSELS IN A FAMILY

      Ophthalmologica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/01/21 alle ore 14:36:33