Search Results

Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study.

• Authors : Limperger V; UKSH, Institute of Clinical Chemistry, Hemostasis Unit, Arnold-Heller-Str. 3 Building 17, Kiel, 24105, Germany. .; Kenet G

Subjects: Blood Group Antigens*/Blood Group Antigens*/Blood Group Antigens*/blood ; Polymorphism, Single Nucleotide*; Prothrombin/Prothrombin/Prothrombin/*genetics

• Source: Journal of thrombosis and thrombolysis [J Thromb Thrombolysis] 2021 Feb; Vol. 51 (2), pp. 494-501.Publisher: Kluwer Academic Publishers Country of Publication: Netherlands NLM ID: 9502018 Publication Model: Print Cited Medium: Internet ISSN:

Record details

National Medical Products Administration of China: Roche Diagnostics voluntarily recalls prothrombin time test card (electrochemical method).

• Source: Contify Life Science News. 2024.

Record details

The prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia.

• Authors : Ehrenforth S; Ludwig G; Klinke S

Subjects: Alleles*; Factor V/Factor V/Factor V/*genetics ; Prothrombin/Prothrombin/Prothrombin/*genetics

• Source: Blood [Blood] 1998 Mar 15; Vol. 91 (6), pp. 2209-10.Publisher: Elsevier Country of Publication: United States NLM ID: 7603509 Publication Model: Print Cited Medium: Print ISSN: 0006-4971 (Print)

Record details

Coagulation factor II activity determination is not useful as a screening tool for the G20210A prothrombin gene allele.

• Authors : Gruenewald M; Germowitz A; Beneke H

Subjects: Alleles*; 3' Untranslated Regions/3' Untranslated Regions/3' Untranslated Regions/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

• Source: Thrombosis and haemostasis [Thromb Haemost] 2000 Jul; Vol. 84 (1), pp. 141-2.Publisher: Thieme Country of Publication: Germany NLM ID: 7608063 Publication Model: Print Cited Medium: Print ISSN:

Record details

Factor V G1691A and prothrombin G20210A in childhood spontaneous venous thrombosis--evidence of an age-dependent thrombotic onset in carriers of factor V G1691A and prothrombin G20210A mutation.

• Authors : Schobess R; Paediatric Haematology and Oncology, University Hospital Halle/Saale. ; Junker R

Subjects: Heterozygote* ; Mutation*; Factor V/Factor V/Factor V/*genetics

• Source: European journal of pediatrics [Eur J Pediatr] 1999 Dec; Vol. 158 Suppl 3, pp. S105-8.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7603873 Publication Model: Print Cited Medium: Print

Record details

Low prevalence of large intraventricular haemorrhage in very low birthweight infants carrying the factor V Leiden or prothrombin G20210A mutation.

• Authors : Göpel W; Department of Pediatrics, University of Lübeck, Germany. ; Gortner L

Subjects: Infant, Very Low Birth Weight* ; Mutation*; Factor V/Factor V/Factor V/*genetics

• Source: Acta paediatrica (Oslo, Norway : 1992) [Acta Paediatr] 2001 Sep; Vol. 90 (9), pp. 1021-4.Publisher: Wiley-Blackwell Country of Publication: Norway NLM ID: 9205968 Publication Model: Print Cited Medium: Print ISSN: 0803-5253 (Print)

Record details

Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester.

• Authors : Pihusch R; Department of Haematology and Oncology, Klinikum der Universität München-Gosshadern, Munich, Germany.; Buchholz T

Subjects: Mutation*; Abortion, Habitual/Abortion, Habitual/Abortion, Habitual/*genetics ; Prothrombin/Prothrombin/Prothrombin/*genetics

• Source: American journal of reproductive immunology (New York, N.Y. : 1989) [Am J Reprod Immunol] 2001 Aug; Vol. 46 (2), pp. 124-31.Publisher: Wiley-Blackwell Country of Publication: Denmark NLM ID: 8912860 Publication Model: Print Cited Medium: Print ISSN: 1046-7408 (Print)

Record details

[Incidence of thrombophilic factor V Leiden and prothrombin G20210A mutation in Perthes disease--a pilot study].

• Authors : Schmitz A; Klinik und Poliklinik für Orthopädie, Rheinischen Friedrich-Wilhelms-Universität Bonn. ; Pförtner J

Subjects: Factor V/Factor V/Factor V/*genetics ; Legg-Calve-Perthes Disease/Legg-Calve-Perthes Disease/Legg-Calve-Perthes Disease/*genetics ; Mutation/Mutation/Mutation/*genetics

• Source: Zeitschrift fur Orthopadie und ihre Grenzgebiete [Z Orthop Ihre Grenzgeb] 2001 Mar-Apr; Vol. 139 (2), pp. 143-6.Publisher: Ferdinand Enke Verlag Country of Publication: Germany NLM ID: 1256465 Publication Model: Print Cited Medium:

Record details

Common genetic coagulation variants are not associated with ischemic stroke in a case-control study.

• Authors : Moskau S; Department of Neurology, University of Bonn, Sigmund-Freud-Strasse 25, 53105 Bonn, Germany.; Smolka K

Subjects: Polymorphism, Genetic*; Brain Ischemia/Brain Ischemia/Brain Ischemia/*genetics ; Factor V/Factor V/Factor V/*genetics

• Source: Neurological research [Neurol Res] 2010 Jun; Vol. 32 (5), pp. 519-22. Date of Electronic Publication: 2009 Aug 05.Publisher: Taylor & Francis Country of Publication: England NLM ID: 7905298 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

Record details

A new PCR-SSP typing method for six single-nucleotide polymorphisms impairing the blood-clotting cascade as well as T-cell stimulation.

• Authors : Meyer M; Department of Transplantation Immunology, University of Heidelberg, Heidelberg, Germany.; Czachurski D

Subjects: Antigens, Differentiation/Antigens, Differentiation/Antigens, Differentiation/*genetics ; Blood Coagulation/Blood Coagulation/Blood Coagulation/*genetics ; CD28 Antigens/CD28 Antigens/CD28 Antigens/*genetics

• Source: Tissue antigens [Tissue Antigens] 2005 Dec; Vol. 66 (6), pp. 650-5.Publisher: Wiley Blackwell Country of Publication: England NLM ID: 0331072 Publication Model: Print Cited Medium: Print ISSN: 0001-2815 (Print)

Record details