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La ricerca find articoli where soggetti phrase all words 'SCLEROCORNEA' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 19 riferimenti
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    1. Hafner, A; Seitz, B
      Masked primary open angle glaucoma in cornea plana by wrongly too low applanation tonometry - a case report

      KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE
    2. Bessant, DAR; Anwar, K; Khaliq, S; Hameed, A; Ismail, M; Payne, AM; Mehdi, SQ; Bhattacharya, SS
      Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32

      BRITISH JOURNAL OF OPHTHALMOLOGY
    3. FORSIUS H; DAMSTEN M; ERIKSSON AW; FELLMAN J; LINDH S; TAHVANAINEN E
      AUTOSOMAL RECESSIVE CORNEA PLANA - A CLINICAL AND GENETIC-STUDY OF 78CASES IN FINLAND

      Acta ophthalmologica Scandinavica
    4. KIM T; COHEN EJ; SCHNALL BM; AFFEL EL; EAGLE RC
      ULTRASOUND BIOMICROSCOPY AND HISTOPATHOLOGY OF SCLEROCORNEA

      Cornea
    5. STRATTON RF; WALTER CA; PAULGAR BR; PRICE ME; MOORE CM
      2ND 46,XX MALE WITH MLS SYNDROME

      American journal of medical genetics
    6. SPRANGER S; STUTE H; BLANKENAGEL A; JAUCH A; HAGER D; TARIVERDIAN G
      OVERLAP IN CLINICAL MANIFESTATIONS BETWEEN CONGENITAL VARICELLA SYNDROME AND MIDAS-SYNDROME, AN X-CHROMOSOMAL DISEASE

      Monatsschrift fur Kinderheilkunde
    7. ZVULUNOV A; KACHKO L; MANOR E; SHINWELL E; CARMI R
      RETICULOLINEAR APLASIA-CUTIS-CONGENITA OF THE FACE AND NECK - A DISTINCTIVE CUTANEOUS MANIFESTATION IN SEVERAL SYNDROMES LINKED TO XP22

      British journal of dermatology
    8. PAULGER BR; KRAUS EW; PULITZER DR; MOORE CM
      XP MICRODELETION SYNDROME CHARACTERIZED BY PATHOGNOMONIC LINEAR SKIN DEFECTS ON THE HEAD AND NECK

      Pediatric dermatology
    9. BELLOSTA M; TRESPIOLLI D; GHISELLI E; CAPRA E; SCAPPATICCI S
      FOCAL DERMAL HYPOPLASIA - REPORT OF A FAMILY WITH 7 AFFECTED WOMEN IN3 GENERATIONS

      EJD. European journal of dermatology
    10. SLEE J; GOLDBLATT J
      FURTHER EVIDENCE FOR A SYNDROME OF APPLE PEEL INTESTINAL ATRESIA, OCULAR ANOMALIES AND MICROCEPHALY

      Clinical genetics
    11. MUCKE J; HOEPFFNER W; THAMM B; THEILE H
      MIDAS SYNDROME (MICROPHTHALMIA, DERMAL APLASIA AND SCLEROCORNEA) - ANAUTONOMOUS ENTITY WITH LINEAR SKIN DEFECTS WITHIN THE SPECTRUM OF FOCAL HYPOPLASIAS

      EJD. European journal of dermatology
    12. WAIZENEGGER UR; KOHNEN T; WEIDLE EG; SCHUTTE E
      CONGENITAL, HEREDITARY CORNEA PLANA COMBI NED WITH PTOSIS, PERIPHERALSCLEROCORNEA AND CONJUNCTIVAL XEROSIS

      Klinische Monatsblatter fur Augenheilkunde
    13. BUSIN M; MELLER D; CUSUMANO A
      ANTERIOR-CHAMBER DYSGENESIS WITH BILATERA L CORNEAL ECTASIA

      Klinische Monatsblatter fur Augenheilkunde
    14. DOANE JF; SAJJADI H; RICHARDSON WP
      BILATERAL PENETRATING KERATOPLASTY FOR SCLEROCORNEA IN AN INFANT WITHMONOSOMY-21 - CASE-REPORT AND REVIEW OF THE LITERATURE

      Cornea
    15. BIRD LM; KROUS HF; EICHENFIELD LF; SWALWELL CI; JONES MC
      FEMALE INFANT WITH ONCOCYTIC CARDIOMYOPATHY AND MICROPHTHALMIA WITH LINEAR SKIN DEFECTS (MLS) - A CLUE TO THE PATHOGENESIS OF ONCOCYTIC CARDIOMYOPATHY

      American journal of medical genetics
    16. MARTINEZFRIAS ML; BERMEJO E; OTERO TS; URIOSTE M; MORENA V; CRUZ E
      NEW SYNDROME - SCLEROCORNEA, HYPERTELORISM, SYNDACTYLY, AND AMBIGUOUSGENITALIA

      American journal of medical genetics
    17. HAPPLE R; DANIELS O; KOOPMAN RJJ
      MIDAS SYNDROME (MICROPHTHALMIA, DERMAL APLASIA, AND SCLEROCORNEA) - AN X-LINKED PHENOTYPE DISTINCT FROM GOLTZ-SYNDROME

      American journal of medical genetics
    18. STROMME P; DAHL E; FLAGE T; STENEJOHANSEN H
      APPLE PEEL INTESTINAL ATRESIA IN SIBLINGS WITH OCULAR ANOMALIES AND MICROCEPHALY

      Clinical genetics
    19. REDBRAKE C; SALLA S; BECKER J; REIM M
      A RARE CASE OF BILATERAL CONGENITAL CORNEAL MALFORMATIONS

      Acta ophthalmologica


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/10/20 alle ore 20:46:23