Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Pierre Hopmeier"'
Autor:
Krzysztof Kucharczyk, Pierre Hopmeier, Alexandra Bezak, Astrid Dossenbach-Glaninger, Werner Lubitz, Radosław Kaczanowski
Publikováno v:
Journal of Clinical Laboratory Analysis. 19:233-240
Factor XI (FXI) deficiency is a rare inherited disorder which can cause bleeding complications especially in case of hemostatic challenge and/or in tissues with high fibrinolytic activity. A number of causative mutations have been described in FXI de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2830e0db20cf4c4eb3e28d72c41ee4bd
https://doi.org/10.1002/jcla.20084
https://doi.org/10.1002/jcla.20084
Autor:
Martin Dossenbach, Astrid Dossenbach-Glaninger, Pierre Hopmeier, Michael van Trotsenburg, Christian Oberkanins, Walter Krugluger, Johannes C. Huber
Publikováno v:
Thrombosis and Haemostasis. 91:694-699
SummaryInherited and acquired thrombophilia are associated with recurrent pregnancy loss. Recently, an increased risk for thromboembolic disease was described for patients with elevated coagulation factor VIII, but it is unknown whether there is also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dd2b3ba67932f974abb7d208d2e32d3
https://doi.org/10.1160/th03-09-0554
https://doi.org/10.1160/th03-09-0554
Autor:
Walter Krugluger, Anne Moritz, Pierre Hopmeier, Astrid Dossenbach-Glaninger, Johannes C. Huber, Michael van Trotsenburg, Martin Dossenbach, Christian Oberkanins
Publikováno v:
Clinical Chemistry. 49:1081-1086
Background: A successful outcome of pregnancy depends on proper placental formation. In the very beginning of this process, trophoblast invasion and fibrin deposition into the wall of the decidual veins play an important part. Two polymorphisms, coag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8417d14ebb5e6739fb9da270cd8203d1
https://doi.org/10.1373/49.7.1081
https://doi.org/10.1373/49.7.1081
Autor:
Claudia Stöllberger, Jörg Slany, Thomas Länger, Barbara Schneider, Pierre Hopmeier, Cornelius Wehinger, Josef Finsterer
Publikováno v:
Journal of Thrombosis and Thrombolysis. 14:65-72
Background: If problems, interventions and complications occurring during oral anticoagulation (OAC) are related with age, indication for OAC, hypertension, diabetes, previous stroke, and number of additional drugs. Material and Methods: Clinical cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f22dc6f2238c874984ae5c84e0c4969
https://doi.org/10.1023/a:1022070406307
https://doi.org/10.1023/a:1022070406307
Autor:
Christian Oberkanins, Johanna Atamaniuk, Pierre Hopmeier, Astrid Dossenbach-Glaninger, Mick van Trotsenburg, Helene Puehringer
Publikováno v:
Clinical Biochemistry, 41(12), 1022-1024. Elsevier Inc.
Hopmeier, P, Puehringer, H, van Trotsenburg, M A A, Atamaniuk, J, Oberkanins, C & Dossenbach-Glaninger, A 2008, ' Association of endothelial protein C receptor haplotypes, factor V Leiden and recurrent first trimester pregnancy loss ', Clinical Biochemistry, vol. 41, no. 12, pp. 1022-1024 . https://doi.org/10.1016/j.clinbiochem.2008.05.004
Hopmeier, P, Puehringer, H, van Trotsenburg, M A A, Atamaniuk, J, Oberkanins, C & Dossenbach-Glaninger, A 2008, ' Association of endothelial protein C receptor haplotypes, factor V Leiden and recurrent first trimester pregnancy loss ', Clinical Biochemistry, vol. 41, no. 12, pp. 1022-1024 . https://doi.org/10.1016/j.clinbiochem.2008.05.004
Objectives We evaluated whether the endothelial protein C receptor (EPCR) haplotypes A1 and A3 exert effects on the development of recurrent pregnancy loss (RPL) in association with factor V Leiden. Design and methods We determined the EPCR haplotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a8b87662fe6c44844bda70e8c462e9e
https://doi.org/10.1016/j.clinbiochem.2008.05.004
https://doi.org/10.1016/j.clinbiochem.2008.05.004
Publikováno v:
Diabetes. 44:1033-1037
Anticoagulant response to activated protein C (APC) was studied in 40 healthy subjects and 67 patients with insulin-dependent diabetes mellitus (IDDM) using a modified activated thromboplastin time assay. Results are expressed in terms of the APC sen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7858b5a1673f52d5923f72ff9c9bfb3d
https://doi.org/10.2337/diabetes.44.9.1033
https://doi.org/10.2337/diabetes.44.9.1033
Autor:
Hans-Peter Kopp, Helga R Nowak, Pierre Hopmeier, Guntram Schernthaner, Christoph Schnack, Nicole Eibl
Publikováno v:
Diabetes Care. 18:188-192
OBJECTIVE To investigate the effects of long-term high-dose oral magnesium (Mg) therapy (30 mmol/day) in patients with type II diabetes. Low plasma magnesium levels have been reported in type II diabetes and are associated with insulin resistance and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::938a604451c310b1b395d507b3a4c183
https://doi.org/10.2337/diacare.18.2.188
https://doi.org/10.2337/diacare.18.2.188
Autor:
Astrid Dossenbach-Glaninger, Mick van Trotsenburg, Pierre Hopmeier, Barbara Schneider, Christian Oberkanins
Publikováno v:
Dossenbach-Glaninger, A, van Trotsenburg, M A A, Schneider, B, Oberkanins, C & Hopmeier, P 2008, ' ACE I/D polymorphism and recurrent first trimester pregnancy loss: interaction with SERPINE1 4G/5G and F13 Val34Leu polymorphisms ', British Journal of Haematology, vol. 141, no. 2, pp. 269-271 . https://doi.org/10.1111/j.1365-2141.2008.07058.x
British Journal of Haematology, 141(2), 269-271. Wiley-Blackwell
British Journal of Haematology, 141(2), 269-271. Wiley-Blackwell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a576d16e752957651a423e757fcebf3e
https://research.vumc.nl/en/publications/21728789-9693-402d-8d2f-66b40a123451
https://research.vumc.nl/en/publications/21728789-9693-402d-8d2f-66b40a123451
Autor:
Astrid Dossenbach-Glaninger, Hanns Helmer, Michael van Trotsenburg, Christian Oberkanins, Pierre Hopmeier
Publikováno v:
Dossenbach-Glaninger, A, van Trotsenburg, M A A, Helmer, H, Oberkanins, C & Hopmeier, P 2008, ' Association of the protein Z intron F G79A gene polymorphism with recurrent pregnancy loss ', Fertility and Sterility, vol. 90, no. 4, pp. 1155-1160 . https://doi.org/10.1016/j.fertnstert.2007.07.1376
Fertility and Sterility, 90(4), 1155-1160. Elsevier Inc.
Fertility and Sterility, 90(4), 1155-1160. Elsevier Inc.
Objective To investigate the association of the common protein Z (PZ) intron F G79A gene polymorphism with recurrent early pregnancy loss (RPL) and its gene-gene interaction with known thrombophilic risk factors for RPL. Design Case control study. Se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d599879c996f33fd771f2cf32f3b34
https://research.vumc.nl/en/publications/20477610-6e96-4bf5-baee-eb84e51dacd3
https://research.vumc.nl/en/publications/20477610-6e96-4bf5-baee-eb84e51dacd3
Publikováno v:
European journal of haematology. 76(4)
Objectives: Hereditary factor XI deficiency is a rare bleeding disorder with worldwide distribution. In Austrian patients only one mutation leading to congenital factor XI deficiency has been reported. In the present study, we identified the molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32d8c618cff87a3f4339615af380d4ac
https://pubmed.ncbi.nlm.nih.gov/16519703
https://pubmed.ncbi.nlm.nih.gov/16519703