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Showing 1 to 5 of 5 for “"Factor V Leiden"”.

  1. Arterial Thrombosis in Factor V Leiden or Activated Protein C Resistance. Clinical and Experimental Studies.

    … Activated protein C (APC) resistance due to Factor V Leiden mutation as the most prevalent genetic risk factor, yet known, for venous thromboembolism. This has been documented in 20-60% of patients with deep vein thrombosis (DVT). Whether such propensity also exists in arterial circulation is …

    lund Repository record for Arterial Thrombosis in Factor V Leiden or Activated Protein C Resistance. Clinical and Experimental Studies. (opens in a new tab)

  2. Evaluation of Current Thrombophilia Screening Practices of Internists, Family Physicians, and Obstetricians/Gynecologists: Factor V Leiden Genetic Testing and Referral Patterns

    <p>Thrombophilia is a complex, multifactorial condition in which the patient exhibits an increased susceptibility to form blood clots, especially in the veins of the lower extremities. A mutation in the gene encoding for factor V, known as factor V Leiden (FVL), is the most common cause of …

    south-carolina Repository record for Evaluation of Current Thrombophilia Screening Practices of Internists, Family Physicians, and Obstetricians/Gynecologists: Factor V Leiden Genetic Testing and Referral Patterns (opens in a new tab)

  3. VENOUS THROMBOEMBOLISM IN SOUTHERN SWEDEN EPIDEMIOLOGY AND RISK FACTORS

    … is still insufficient information on VTE risk factors and patient characteristics in the general population. Previously published incidences of VTE (deep venous thrombosis [DVT] and pulmonary embolism [PE]) vary from 71 to 192 per 100,000 individuals per year. Incidences of DVT and PE have been …

    lund Repository record for VENOUS THROMBOEMBOLISM IN SOUTHERN SWEDEN EPIDEMIOLOGY AND RISK FACTORS (opens in a new tab)

  4. Επιπλοκές της κύησης σε γυναίκες ελληνικής καταγωγής με κληρονομική θρομβοφιλία

    … συχνές θρομβοφιλικές μεταλλάξεις (παράγοντας V Leiden, G20210A πολυμορφισμός του παράγοντα II, C677T πολυμορφισμός του MTHFR γονιδίου) και παρακολουθήθηκαν για δυσμενή έκβαση της εγκυμοσύνης. Οι συγκρίσεις μεταξύ των ομάδων πραγματοποιήθηκαν με τη δοκιμασία Pearson’s x2 και υπολογίστηκε το Odds …

    patras-thes Repository record for Επιπλοκές της κύησης σε γυναίκες ελληνικής καταγωγής με κληρονομική θρομβοφιλία (opens in a new tab)

  5. Trombose da veia porta em crianças e adolescentes : deficiência das proteínas C, S e antitrombina e pesquisa das mutações fator V Leiden, G20210A da protrombina e C677T da metileno-tetraidrofolato redutase

    … C, S e antitrombina − e das mutações fator V Leiden, G20210A no gene da protrombina e C677T da metileno-tetraidrofolato redutase em crianças e adolescentes com trom-bose da veia porta, definir o padrão hereditário de uma eventual deficiência das pro-teínas inibidoras da coagulação nesses …

    brazil-ufrgs Repository record for Trombose da veia porta em crianças e adolescentes : deficiência das proteínas C, S e antitrombina e pesquisa das mutações fator V Leiden, G20210A da protrombina e C677T da metileno-tetraidrofolato redutase (opens in a new tab)