Search Results

Display Settings
Results per page: 10
Sort By: Relevance
Filter
  • 1-10 of  11 results for ""Hypoprothrombinemias""

Your Filters

Publisher : ferrata storti foundation
Reset filters
Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Report

Prothrombin Suresnes: a case of homozygous F299V mutation responsible for hypodysprothrombinemia.

Subjects: Homozygote* ; Mutation*; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*blood

  • Source: Haematologica [Haematologica] 2006 Mar; Vol. 91 (3), pp. 431-2. Date of Electronic Publication: 2006 Feb 17.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print-Electronic Cited

Record details

Read More Add to Saved list
×
Report

Successful treatment of acquired hypoprothrombinemia without associated lupus anticoagulant using intravenous immunoglobulin.

Subjects: Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*drug therapy ; Immunoglobulins, Intravenous/Immunoglobulins, Intravenous/Immunoglobulins, Intravenous/*administration & dosage; Aged

  • Source: Haematologica [Haematologica] 2001 May; Vol. 86 (5), pp. 551.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Severe bleeding due to acquired hypoprothrombinemia-lupus anticoagulant syndrome. Case report and review of literature.

  • Authors : Vivaldi P; Department of Medicine II, S. Chiara General Hospital, Trento, Italy.; Rossetti G

Subjects: Antiphospholipid Syndrome/Antiphospholipid Syndrome/Antiphospholipid Syndrome/*complications ; Autoimmune Diseases/Autoimmune Diseases/Autoimmune Diseases/*complications ; Hemorrhage/Hemorrhage/Hemorrhage/*etiology

  • Source: Haematologica [Haematologica] 1997 May-Jun; Vol. 82 (3), pp. 345-7.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Report

A natural variant with a point mutation resulting in a homozygous Arg to His substitution at position 388 in prothrombin.

Subjects: Genetic Variation* ; Homozygote* ; Point Mutation*

  • Source: Haematologica [Haematologica] 2008 May; Vol. 93 (5), pp. 799-800.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

[Contribution to the study of idiopathic hypoprothrombinemia. (Clinical case)].

Subjects: Hemorrhagic Disorders* ; Hemostatics* ; Hypoprothrombinemias*

  • Source: Haematologica [Haematologica] 1961; Vol. 46, pp. 1062-72.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

[Studies on certain hemorrhagic syndrome with hypoprothrombinemia and with thrombocytopenia].

Subjects: Blood Platelets* ; Hemorrhagic Disorders* ; Hypoprothrombinemias*

  • Source: Haematologica [Haematologica] 1953; Vol. 37 (3), pp. 245-94.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

Simultaneous detection of FV Q506 and prothrombin 20210 A variation by allele-specific PCR.

  • Authors : Mitterer M; Department of Hematology and Bone Marrow Transplantation Center, L. Boehlerstrasse Nr. 5, I-39031 Bozen/Bolzano, Italy. ; Lanthaler AJ

Subjects: Point Mutation*; Activated Protein C Resistance/Activated Protein C Resistance/Activated Protein C Resistance/*genetics ; DNA Mutational Analysis/DNA Mutational Analysis/DNA Mutational Analysis/*methods

  • Source: Haematologica [Haematologica] 1999 Mar; Vol. 84 (3), pp. 204-7.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Editorial & Opinion

Hypoprothrombinemia in patients receiving cefotetan.

Subjects: Cefotetan/Cefotetan/Cefotetan/*adverse effects ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*chemically induced; Aged

  • Source: Haematologica [Haematologica] 1990 Mar-Apr; Vol. 75 (2), pp. 196.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

[Parahemophilia in the neonatal age: details of the pathogenetic and clinical description and therapeutic aspects].

Subjects: Infant, Newborn, Diseases*; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*etiology ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*therapy

  • Source: Haematologica [Haematologica] 1966; Vol. 51 (9), pp. 705-24.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
Academic Journal

[Therapy of hemorrhagic syndrome due to factor V deficiency].

Subjects: Hemorrhage/Hemorrhage/Hemorrhage/*therapy ; Hypoprothrombinemias/Hypoprothrombinemias/Hypoprothrombinemias/*therapy; Adolescent

  • Source: Haematologica [Haematologica] 1971; Vol. 56 (9), pp. 430-3.Publisher: Ferrata Storti Foundation Country of Publication: Italy NLM ID: 0417435 Publication Model: Print Cited Medium:

Record details

Read More Add to Saved list
×
  • 1-10 of  11 results for ""Hypoprothrombinemias""