يعرض 1 - 3 نتائج من 3 نتيجة بحث عن '"G L, Tiscia"', وقت الاستعلام: 0.35s تنقيح النتائج
  1. 1
    Academic Journal
    Obstetric complications and pregnancy-related venous thromboembolism: the effect of low molecular weight heparin on their prevention in carriers of factor V leiden or prothrombin G20210A mutation

    المؤلفون: TORMENE, DANIELA, SIMIONI, PAOLO, E. Grandone, V. De Stefano, A. Tosetto, G. Palareti, M. Margaglione, G. Castaman, E. Rossi, A. Ciminello, L. Valdrè, C. Legnani, G. L. Tiscia, V. Bafunno, S. Carraro, F. Rodeghiero

    المساهمون: Tormene, Daniela, E., Grandone, V., De Stefano, A., Tosetto, G., Palareti, M., Margaglione, G., Castaman, E., Rossi, A., Ciminello, L., Valdrè, C., Legnani, G. L., Tiscia, V., Bafunno, S., Carraro, F., Rodeghiero, Simioni, Paolo

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000302495200011; volume:107; journal:THROMBOSIS AND HAEMOSTASIS; http://hdl.handle.net/11577/2490672; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84857732644

    الاتاحة: http://hdl.handle.net/11577/2490672
    https://doi.org/10.1160/TH11-07-0470

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  2. 2
    Academic Journal
    Occurrence of the JAK2 V617F mutation in the Budd–Chiari Syndrome

    المؤلفون: D. COLAIZZO, L. AMITRANO, G. L. TISCIA, L. IANNACCONE, E. GRANDONE, M. A. GUARDASCIONE AND M. MARGAGLIONE, GALLONE, Anna

    المساهمون: D., Colaizzo, L., Amitrano, G. L., Tiscia, L., Iannaccone, Gallone, Anna, E., Grandone, M. A. GUARDASCIONE AND M., Margaglione

    مصطلحات موضوعية: AK2 V617F mutation, Budd-Chiari syndrome, myeloproliferative disease, thrombosi, KeyWords Plus: SPLANCHNIC VEIN-THROMBOSIS, POLYCYTHEMIA-VERA, ESSENTIAL THROMBOCYTHEMIA, VENOUS THROMBOSIS, MYELOPROLIFERATIVE DISORDERS, ACTIVATING MUTATION, MYELOID METAPLASIA, RISK-FACTOR, GENE, MYELOFIBROSIS

    Relation: info:eu-repo/semantics/altIdentifier/pmid/18600100; info:eu-repo/semantics/altIdentifier/wos/WOS:000257927600022; volume:19(5); firstpage:459; lastpage:462; numberofpages:4; journal:BLOOD COAGULATION & FIBRINOLYSIS; http://hdl.handle.net/11586/49437; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-59949094293

    الاتاحة: http://hdl.handle.net/11586/49437

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  3. 3
    Factor XI deficiency: two novel mutations in asymptomatic Italian patients

    المؤلفون: M, Tomaiuolo, G, Favuzzi, F, Cappucci, D, Pisanelli, G L, Tiscia, P, Musto, F A, Scaraggi, R I, Cincione, M, Margaglione, E, Grandone

    المصدر: Haemophilia : the official journal of the World Federation of Hemophilia. 16(5)

    مصطلحات موضوعية: Phenotype, Italy, Factor XI Deficiency, DNA Mutational Analysis, Mutation, Missense, Humans, Female, Genetic Predisposition to Disease, Middle Aged, Factor XI, White People, Aged

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::0757f0e19b5e68ebb758bb015f854565
    https://pubmed.ncbi.nlm.nih.gov/20491955

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