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La ricerca find articoli where authors phrase all words ' HORDT M' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 16 riferimenti
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    1. HAVERKAMP W; HORDT M; BREITHARDT G; BORGGREFE M
      TORSADE-DE-POINTES SECONDARY TO D,L-SOTALOL AFTER CATHETER ABLATION OF INCESSANT ATRIOVENTRICULAR REENTRANT TACHYCARDIA - EVIDENCE FOR A SIGNIFICANT CONTRIBUTION OF THE CARDIAC MEMORY

      Clinical cardiology
    2. SCHULZEBAHR E; WANG Q; WEDEKIND H; HAVERKAMP W; CHEN QY; SUN YL; RUBIE C; HORDT M; TOWBIN JA; BORGGREFE M; ASSMANN G; QU XD; SOMBERG JC; BREITHARDT G; OBERTI C; FUNKE H
      KCNE1 MUTATIONS CAUSE JERVELL AND LANGE-NIELSEN-SYNDROME

      Nature genetics
    3. SCHULZEBAHR E; HAVERKAMP W; WEDEKIND H; RUBIE C; HORDT M; BORGGREFE M; ASSMANN G; BREITHARDT G; FUNKE H
      AUTOSOMAL RECESSIVE LONG-QT SYNDROME (JERVELL LANGE-NIELSEN SYNDROME)IS GENETICALLY HETEROGENEOUS

      Human genetics
    4. SCHULZEBAHR E; WANG Q; HAVERKAMP W; WEDEKIND H; RUBIE C; CHEN QY; HORDT M; BREITHARDT G; FUNKE H
      IDENTIFICATION OF A NEW GENE FOR AUTOSOMAL RECESSIVE LONG-CT SYNDROME(JERVELL-LANGE-NIELSEN-SYNDROME)

      Circulation
    5. SCHULZEBAHR E; HAVERKAMP W; HORDT M; WEDEKIND H; BORGGREFE M; FUNKE H
      DO MUTATIONS IN CARDIAC ION-CHANNEL GENES PREDISPOSE TO DRUG-INDUCED (ACQUIRED) LONG-QT SYNDROME

      Circulation
    6. WEDEKIND H; SCHULZEBAHR E; HAVERKAMP W; HORDT M; LANGE S; RUBLE C; BORGGREFE M; FUNKE H
      GENE WITH GENE INTERACTION INFLUENCES THE EXPRESSIVITY IN CHROMOSOME 11-SPECIFIC (KVLQT1) LONG-QT SYNDROME IN A LARGE GERMAN KINDRED

      Circulation
    7. SCHULZEBAHR E; WANG Q; WEDEKIND H; HAVERKAMP W; CHEN Q; SUN Y; RUBIE C; HORDT M; TOWBIN JA; BORGGREFE M; ASSMANN G; QU X; SOMBERG JC; BREITHARDT G; OBERTI C; FUNKE H
      IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL GENE FOR AUTOSOMAL RECESSIVE DEAFNESS AND LONG-QT SYNDROME (JERVELL AND LANGE-NIELSEN-SYNDROME)

      American journal of human genetics
    8. WEDEKIND H; SCHULZEBAHR E; LANGE S; RUBIE C; HAVERKAMP W; HORDT M; BORGGREFE M; ASSMANN G; BREITHARDT G; FUNKE H
      A SEVERE FORM OF LONG-QT SYNDROME CAUSED BY 2 KVLQT1 MUTATIONS LOCATED IN CIS

      American journal of human genetics
    9. SCHULZEBAHR E; HAVERKAMP W; WIEBUSCH H; WEDEKIND H; HORDT M; BORGGREFE M; BREITHARDT G; FUNKE H
      FREQUENCY AND PHENOTYPE OF HERG MUTATIONS IN CONGENITAL LONG QT SYNDROME (LQTS)

      Circulation
    10. SCHULZEBAHR E; HAVERKAMP W; WIEBUSCH H; SCHULTE H; HORDT M; BORGGREFE M; BREITHARDT G; ASSMANN G; FUNKE H
      MOLECULAR ANALYSIS AT THE HARVEY RAS-1 GENE IN PATIENTS WITH LONG QT SYNDROME

      Journal of molecular medicine
    11. HAVERKAMP W; HORDT M; BORGGREFE M; BREITHARDT G
      TORSADE-DE-POINTES AND THE QT SYNDROME

      Medizinische Klinik
    12. HORDT M; HAVERKAMP W; OBERWITTLER C; LUDEMANN P; BORGGREFE M; RINGELSTEIN EB; BREITHARDT G
      THE IDIOPATHIC LONG QT SYNDROME AS A CAUS E OF EPILEPTIC AND NONEPILEPTIC ATTACKS

      Nervenarzt
    13. HAVERKAMP W; WICHTER T; CHEN X; HORDT M; WILLEMS S; ROTMAN B; HINDRICKS G; KOTTKAMP H; BORGGREFE M; BREITHARDT G
      PROARRHYTHMIC EFFECTS OF ANTIARRHYTHMIC D RUGS

      Zeitschrift fur Kardiologie
    14. HAVERKAMP W; HORDT M; WILLEMS S; KOTTKAMP H; HINDRICKS G; BORGGREFE M; BREITHARDT G
      POLYMORPHIC VENTRICULAR-TACHYCARDIA OR TO RSADE-DE-POINTES

      Herz, Kreislauf
    15. HAVERKAMP W; HORDT M; CHEN X; HINDRICKS G; WILLEMS S; KOTTKAMP H; ROTMAN B; BRUNN J; BORGGREFE M; BREITHARDT G
      TORSADE-DE-POINTES

      Zeitschrift fur Kardiologie
    16. HAVERKAMP W; HORDT M; CHEN X; WILLEMS S; BRUNN J; ROTMAN B; BORGGREFE M
      TORSADES-DE-POINTES INDUCED BY D,L-SOTALOL

      Circulation


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 05/08/20 alle ore 10:27:59