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La ricerca find articoli where authors phrase all words ' PONJAVIC V' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. Eksandh, LC; Ponjavic, V; Ayyagari, R; Bingham, EL; Hiriyanna, KT; Andreasson, S; Ehinger, B; Sieving, PA
      Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene

      ARCHIVES OF OPHTHALMOLOGY
    2. EKSTROM U; ANDREASSON S; PONJAVIC V; ABRAHAMSON M; SANDGREN O; NILSSONEHLE P; EHINGER B
      A SWEDISH FAMILY WITH A MUTATION IN THE PERIPHERIN RDS GENE (ARG-172-TRP) ASSOCIATED WITH A PROGRESSIVE RETINAL DEGENERATION/

      Ophthalmic genetics
    3. EKSTROM U; PONJAVIC V; ABRAHAMSON M; NILSSONEHLE P; ANDREASSON S; STENSTROM I; EHINGER B
      PHENOTYPIC-EXPRESSION OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA IN ASWEDISH FAMILY EXPRESSING A PHE-211-LEU VARIANT OF PERIPHERIN RDS/

      Ophthalmic genetics
    4. EKSTROM U; PONJAVIC V; ANDREASSON S; EHINGER B; NILSSONEHLE P; ABRAHAMSON M
      DETECTION OF ALTERATIONS IN ALL 3 EXONS OF THE PERIPHERIN RDS GENE INSWEDISH PATIENTS WITH RETINITIS-PIGMENTOSA USING AN EFFICIENT DGGE SYSTEM/

      Journal of clinical pathology-Molecular pathology
    5. PONJAVIC V; ABRAHAMSON M; ANDREASSON S; EHINGER B; FEX G
      AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA WITH A RHODOPSIN MUTATION (ARG-135-TRP) - DISEASE PHENOTYPE IN A SWEDISH FAMILY

      Acta ophthalmologica Scandinavica
    6. PONJAVIC V; ABRAHAMSON M; ANDREASSON S; EHINGER B; FEX G; POLLAND W
      A MILD PHENOTYPE OF AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA IS ASSOCIATED WITH THE RHODOPSIN MUTATION PRO-267-LEU

      Ophthalmic genetics
    7. PONJAVIC V; EKSTROM U; ANDREASSON S; ABRAHAMSON M; NILSSONEHLE P; STENSTROM I; EHINGER B
      PHENOTYPE IN A SWEDISH FAMILY WITH AUTOSOMAL-DOMINANT RETINITIS-PIGMENTOSA AND A POINT MUTATION (PHE-211-LEU) IN THE PERIPHERIN RDS GENE/

      Investigative ophthalmology & visual science
    8. ANDREASSON S; PONJAVIC V; ABRAHAMSON M; EHINGER B; WU W; FUJITA R; BURACZYNSKA M; SWAROOP A
      PHENOTYPES IN 3 SWEDISH FAMILIES WITH X-LINKED RETINITIS-PIGMENTOSA CAUSED BY DIFFERENT MUTATIONS IN THE RPGR GENE

      American journal of ophthalmology
    9. PONJAVIC V; ANDREASSON S; TRANEBJAERG L; LUBS HA
      FULL-FIELD ELECTRORETINOGRAMS IN A FAMILY WITH MOHR-TRANEBJAERG SYNDROME

      Acta ophthalmologica Scandinavica
    10. ANDREASSON S; PONJAVIC V
      FULL-FIELD ELECTRORETINOGRAMS IN INFANTS WITH HEREDITARY TAPETORETINAL DEGENERATION

      Acta ophthalmologica Scandinavica
    11. PONJAVIC V; ANDREASSON SO; ERIKSEN H; TRANEBJAERG L; EHINGER B
      FULL-FIELD ELECTRORETINOGRAMS IN A 3 GENERATION FAMILY WITH DOMINANT CONE-ROD DYSTROPHY

      Investigative ophthalmology & visual science
    12. PONJAVIC V; ABRAHAMSON M; ANDREASSON S; VANBOKHOVEN H; CREMERS FPM; EHINGER B; FEX G
      PHENOTYPE VARIATIONS WITHIN A CHOROIDEREMIA FAMILY LACKING THE ENTIRECHM GENE

      Ophthalmic genetics
    13. PONJAVIC V; ABRAHAMSON M; ANDREASSON S; VANBOKHOVEN H; CREMERS FPM; EHINGER B; FEX G
      VARIATIONS IN FULL FIELD ELECTRORETINOGRAMS AND PHENOTYPES WITHIN A FAMILY WITH CHOROIDEREMIA AND A COMPLETE DELETION OF THE CHM GENE/

      Investigative ophthalmology & visual science
    14. TRANEBJAERG L; SCHWARTZ C; ERIKSEN H; ANDREASSON S; PONJAVIC V; DAHL A; STEVENSON RE; MAY M; ARENA F; BARKER D; ELVERLAND HH; LUBS H
      A NEW X-LINKED RECESSIVE DEAFNESS SYNDROME WITH BLINDNESS, DYSTONIA, FRACTURES, AND MENTAL DEFICIENCY IS LINKED TO XQ22

      Journal of Medical Genetics
    15. PONJAVIC V; ANDREASSON S; EHINGER B
      FULL-FIELD ELECTRORETINOGRAMS IN PATIENTS WITH CENTRAL AREOLAR CHOROIDAL DYSTROPHY

      Acta ophthalmologica
    16. ANDREASSON S; PONJAVIC V; EHINGER B
      FULL-FIELD ELECTRORETINOGRAM IN A PATIENT WITH CUTANEOUS MELANOMA-ASSOCIATED RETINOPATHY

      Acta ophthalmologica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 30/10/20 alle ore 19:15:29