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La ricerca find articoli where soggetti phrase all words 'FACTOR-XI DEFICIENCY' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 51 riferimenti
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    1. Ostrer, H
      A genetic profile of contemporary Jewish populations

      NATURE REVIEWS GENETICS
    2. Billon, S; Blouch, MT; Escoffre-Barbe, M; Le Niger, C; Le Roux, AM; Abgrall, JF
      A case of chronic myelomonocytic leukaemia and factor XI deficiency with acirculating anticoagulant

      HAEMOPHILIA
    3. Aledort, LM
      Making a therapeutic choice: human versus recombinant fractions - can we do it?

      HAEMOPHILIA
    4. Bouma, BN; Marx, PF; Mosnier, LO; Meijers, JCM
      Thrombin-activatable fibrinolysis inhibitor (TAFI, plasma procarboxypeptidase B, procarboxypeptidase R, procarboxypeptidase U)

      THROMBOSIS RESEARCH
    5. Corral, J; Iniesta, JA; Gonzalez-Conejero, R; Villalon, M; Vicente, V
      Polymorphisms of clotting factors modify the risk for primary intracranialhemorrhage

      BLOOD
    6. Teruya, J; Styler, M
      Management of factor XI inhibitor for cardiac intervention: successful treatment with immunosuppressive therapy and plasma exchange

      HAEMOPHILIA
    7. Kawaguchi, T; Koga, S; Hongo, H; Komiyama, Y; Li, K; Ishihara, S; Horikawa, K; Hidaka, M; Mitsuya, H; Nakakuma, H
      A novel type of factor XI deficiency showing compound genetic abnormalities: A nonsense mutation and an impaired transcription

      INTERNATIONAL JOURNAL OF HEMATOLOGY
    8. Franchini, M; de Gironcoli, M; Lippi, G; Manzato, F; Aprili, G; Gandini, G
      Prophylactic use of desmopressin in surgery of six patients with symptomatic heterozygous factor XI deficiency

      HAEMATOLOGICA
    9. Yang, TL; Cui, JS; Taylor, JM; Yang, A; Gruber, SB; Ginsburg, D
      Rescue of fatal neonatal hemorrhage in factor V deficient mice by low level transgene expression

      THROMBOSIS AND HAEMOSTASIS
    10. Kadir, RA; Aledort, LM
      Obstetrical and gynaecological bleeding: a common presenting symptom

      CLINICAL AND LABORATORY HAEMATOLOGY
    11. Iijima, K; Udagawa, A; Kawasaki, H; Murakami, F; Shimomura, T; Ikawa, S
      A factor XI deficiency associated with a nonsense mutation (Trp501stop) inthe catalytic domain

      BRITISH JOURNAL OF HAEMATOLOGY
    12. Diaz, GA; Gelb, BD; Risch, N; Nygaard, TG; Frisch, A; Cohen, IJ; Miranda, CS; Amaral, O; Maire, I; Poenaru, L; Caillaud, C; Weizberg, M; Mistry, P; Desnick, RJ
      Gaucher disease: The origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations

      AMERICAN JOURNAL OF HUMAN GENETICS
    13. Colombo, R
      Age estimate of the N370S mutation causing Gaucher disease in Ashkenazi Jews and European populations: A reappraisal of haplotype data

      AMERICAN JOURNAL OF HUMAN GENETICS
    14. Economides, DL; Kadir, RA
      Inherited bleeding disorders in obstetrics and gynaecology

      BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY
    15. Bolton-Maggs, PHB
      Bleeding problems in factor XI deficient women

      HAEMOPHILIA
    16. Bauduer, F; Dupreuilh, F; Ducout, L; Marti, B
      Factor XI deficiency in the French Basque Country

      HAEMOPHILIA
    17. Kadir, RA; Economides, DL; Sabin, CA; Pollard, D; Lee, CA
      Assessment of menstrual blood loss and gynaecological problems in patientswith inherited bleeding disorders

      HAEMOPHILIA
    18. Young, G; Driscoll, MC
      Coagulation abnormalities in the carbohydrate-deficient glycoprotein syndrome: Case report and review of the literature

      AMERICAN JOURNAL OF HEMATOLOGY
    19. Minnema, MC; Ten Cate, H; Hack, CE
      The role of factor XI in coagulation: A matter of revision

      SEMINARS IN THROMBOSIS AND HEMOSTASIS
    20. Kadir, RA
      Women and inherited bleeding disorders: Pregnancy and delivery

      SEMINARS IN HEMATOLOGY
    21. Mitchell, M; Cutler, J; Thompson, S; Moore, G; ap Rees, EJ; Smith, M; Savidge, G; Alhaq, A
      Heterozygous factor XI deficiency associated with three novel mutations

      BRITISH JOURNAL OF HAEMATOLOGY
    22. Alhaq, A; Mitchell, M; Sethi, M; Rahman, S; Flynn, G; Boulton, P; Caeno, G; Smith, M; Savidge, G
      Identification of a novel mutation in a non-Jewish factor XI deficient kindred

      BRITISH JOURNAL OF HAEMATOLOGY

    23. A MEETING HELD IN LONDON, 12-13 JANUARY 1998, TO DISCUSS BLEEDING DISORDERS IN WOMEN

      Haemophilia
    24. Kadir, RA; Sabin, CA; Pollard, D; Lee, CA; Economides, DL
      Quality of life during menstruation in patients with inherited bleeding disorders

      HAEMOPHILIA
    25. UEN WC; CHOU YH; LIU CC; LIN SM; CHEN TJ
      SUCCESSFUL RESECTION OF SIGMOID COLON-CANCER IN A PATIENT WITH FACTOR-XI DEFICIENCY

      Journal of the Formosan Medical Association
    26. KADIR RA; ECONOMIDES DL; SABIN CA; OWENS D; LEE CA
      FREQUENCY OF INHERITED BLEEDING DISORDERS IN WOMEN WITH MENORRHAGIA

      Lancet
    27. MINNEMA MC; FRIEDERICH PW; LEVI M; VONDEMBORNE PAK; MOSNIER LO; MEIJERS JCM; BIEMOND BJ; HACK CE; BOUMA BN; TENCATE H
      ENHANCEMENT OF RABBIT JUGULAR-VEIN THROMBOLYSIS BY NEUTRALIZATION OF FACTOR-XI - IN-VIVO EVIDENCE FOR A ROLE OF FACTOR-XI AS AN ANTI-FIBRINOLYTIC FACTOR

      The Journal of clinical investigation
    28. Sherer, Y; Bar-Zohar, D; Levy, Y; Shoenfeld, Y
      Thromboembolic phenomena in patients with hereditary factor XI deficiency

      ANNALES DE MEDECINE INTERNE
    29. SINGER ST; HURST D; ADDIEGO JE
      BLEEDING DISORDERS IN NOONAN-SYNDROME - 3 CASE-REPORTS AND REVIEW OF THE LITERATURE

      Journal of pediatric hematology/oncology
    30. EVANS G; PASI KJ; MEHTA A; LEE CA; PERRY DJ
      RECURRENT VENOUS THROMBOEMBOLIC DISEASE AND FACTOR-XI CONCENTRATE IN A PATIENT WITH SEVERE FACTOR-XI DEFICIENCY, CHRONIC MYELOMONOCYTIC LEUKEMIA, FACTOR-V-LEIDEN AND HETEROZYGOUS PLASMINOGEN DEFICIENCY

      Blood coagulation & fibrinolysis
    31. WISTINGHAUSEN B; REISCHER A; ODDOUX C; OSTRER H; NARDI M; KARPATKIN M
      SEVERE FACTOR-XI DEFICIENCY IN AN ARAB FAMILY ASSOCIATED WITH A NOVELMUTATION IN EXON-11

      British Journal of Haematology
    32. RICHARDS EM; MAKRIS MM; COOPER P; PRESTON FE
      IN-VIVO COAGULATION ACTIVATION FOLLOWING INFUSION OF HIGHLY PURIFIED FACTOR-XI CONCENTRATE

      British Journal of Haematology
    33. PLUCHET S; ABECASSIS L; DINULESCU T; PORTE A; AUCEREAU F; BABOU F; POUPIN F
      CONGENITAL CLOTTING FACTOR DEFICIENCIES - MANAGEMENT DURING SURGERY -EVALUATION OF 10 YEARS ACTIVITY AT THE AULNAY-SOUS-BOIS AND SAINT-DENIS HOSPITALS

      Annales de chirurgie
    34. MASSARANO AA; WOOD A; TAIT RC; STEVENS R; SUPER M
      NOONAN SYNDROME - COAGULATION AND CLINICAL ASPECTS

      Acta paediatrica
    35. BLANCHARD N; JEANJEAN P; LEPOINTE F; DIEVAL J; OSSART M
      FACTOR-XI DEFICIENCY, A NEW SUBSTITUTE - THE HUMAN PURIFIED CONCENTRATES

      Annales francaises d'anesthesie et de reanimation
    36. PERNOD G; VINCIGUERRA C; GAUCHER C; MAZURIER C; POLACK B; NEGRIER C
      COMBINED HEREDITARY DISORDERS OF HEMOPHILIA-B LEYDEN (-6G-]A) AND TYPE-1 VON-WILLEBRAND DISEASE

      Thrombosis and haemostasis
    37. PLUCHET S; ABECASSIS L; DINULESCU T; PORTE A; AUCEREAU F; BABOU F; POUPIN E
      CONGENITAL CLOTTING FACTOR DEFICIENCIES - MANAGEMENT DURING SURGERY -EVALUATION OF 10 YEARS ACTIVITY AT THE AULNAY-SOUS-BOIS AND SAINT-DENIS HOSPITALS

      La Semaine des hopitaux de Paris
    38. CASTAMAN G; RUGGERI M; RODEGHIERO F
      CLINICAL USEFULNESS OF DESMOPRESSIN FOR PREVENTION OF SURGICAL BLEEDING IN PATIENTS WITH SYMPTOMATIC HETEROZYGOUS FACTOR-XI DEFICIENCY

      British Journal of Haematology
    39. NICHOLS WC; AMANO K; CACHERIS PM; FIGUEIREDO MS; MICHAELIDES K; SCHWAAB R; HOYER L; KAUFMAN RJ; GINSBURG D
      MODERATION OF HEMOPHILIA-A PHENOTYPE BY THE FACTOR-V R506Q MUTATION

      Blood
    40. LUSHER JM
      SCREENING AND DIAGNOSIS OF COAGULATION DISORDERS

      American journal of obstetrics and gynecology
    41. BOLTONMAGGS P
      FACTOR-XI DEFICIENCY - A REVIEW

      Haemophilia
    42. COLLINS PW; GOLDMAN E; LILLEY P; PASI KJ; LEE CA
      CLINICAL-EXPERIENCE OF FACTOR-XI DEFICIENCY - THE ROLE OF FRESH-FROZEN PLASMA AND FACTOR-XI CONCENTRATE

      Haemophilia
    43. BRENNER B; STEINBERG T; LAOR A; TAVORI S; TATARSKY I; LANIR N
      VON-WILLEBRAND-FACTOR ANTIGEN AND FACTOR-XI ACTIVITY LEVELS AS PREDICTORS OF BLEEDING TENDENCY IN ISRAELI PATIENTS WITH VON WILLEBRANDS DISEASE

      Clinical and applied thrombosis/hemostasis
    44. BOLTONMAGGS PHB; HILL FGH
      THE RARER INHERITED COAGULATION DISORDERS - A REVIEW

      Blood reviews
    45. LERUT JP; LATERRE PF; LAVENNEPARDONGE E; DONATACCIO M; GEUBEL A; REYNAERT MS; OTTE JB
      LIVER-TRANSPLANTATION AND HEMOPHILIA-A

      Journal of hepatology
    46. IMANAKA Y; LAL K; NISHIMURA T; BOLTONMAGGS PHB; TUDDENHAM EGD; MCVEY JH
      IDENTIFICATION OF 2 NOVEL MUTATIONS IN NON-JEWISH FACTOR-XI DEFICIENCY

      British Journal of Haematology
    47. BERG LP; VARON D; MARTINOWITZ U; WIELAND K; KAKKAR VV; COOPER DN
      COMBINED FACTOR-VIII FACTOR-XI DEFICIENCY MAY CAUSE INTRA-FAMILIAL CLINICAL VARIABILITY IN HEMOPHILIA-A AMONG ASHKENAZI JEWS

      Blood coagulation & fibrinolysis
    48. KOTTKEMARCHANT K
      LABORATORY DIAGNOSIS OF HEMORRHAGIC AND THROMBOTIC DISORDERS

      Hematology/oncology clinics of North America
    49. SELIGSOHN U; PERETZ H
      MOLECULAR-GENETICS ASPECTS OF FACTOR-XI DEFICIENCY AND GLANZMANN THROMBASTHENIA

      Haemostasis
    50. SANO M; SAITO H; SHIMAMOTO Y; SUGIURA I; OHTSUBO H; KOHDA H; YAMAGUCHI M
      COMBINED HEREDITARY FACTOR-XI (PLASMA THROMBOPLASTIN ANTECEDENT) DEFICIENCY, VON-WILLEBRANDS DISEASE, AND XERODERMA-PIGMENTOSUM IN A JAPANESE FAMILY

      American journal of hematology
    51. SHAPIRO N
      WHEN THE BLEEDING WONT STOP - A CASE-REPORT ON A PATIENT WITH HEMOPHILIA

      The Journal of the American Dental Association


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 08/08/20 alle ore 09:29:29