Zobrazeno 1 - 10
of 66
pro vyhledávání: '"L, Kochhan"'
Publikováno v:
Thrombosis Research. 128:498-500
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9e140346d2ba9b9b5793547bf2324ab
https://doi.org/10.1016/j.thromres.2011.06.012
https://doi.org/10.1016/j.thromres.2011.06.012
Publikováno v:
Fetal Diagnosis and Therapy. 16:211-214
Objectives: Nuchal translucency measurement of 3 mm or more (≧95th centile for gestation age), hydrops fetalis or hygroma colli between the 11th and 14th weeks of gestation is associated with a higher risk of fetal Down syndrome and other aneuploid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2f8cccd5665e406c01880568ee805366
https://doi.org/10.1159/000053912
https://doi.org/10.1159/000053912
Publikováno v:
Hämostaseologie. 30:162-164
SummaryA 17-year old man was sent to us for coagulation testing because he suffered from acute bleeding which started immediately after making an incision in the skin for a urological surgery. The patient had a history of mild bleeding symptoms (nose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acf0222552785f1854f41e7766b2371a
https://doi.org/10.1055/s-0037-1619046
https://doi.org/10.1055/s-0037-1619046
Publikováno v:
Hämostaseologie. 29:187-189
SummaryA 14 year old boy was referred to us for a detailed coagulation study because a previously performed aPTT has been found prolonged. The boy had no history of bleeding symptoms and also the family history was negative for bleeding or thrombotic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03162da86fb230daa62888c97c1c721d
https://doi.org/10.1055/s-0037-1617022
https://doi.org/10.1055/s-0037-1617022
Publikováno v:
Hämostaseologie. 19:77-85
ZusammenfassungDie rasante Entwicklung in der Aufklärung angeborener Gerinnungsdefekte, nicht zuletzt durch den Einsatz der molekulargenetischen Diagnostik, hat die Erfolgsrate bei der Ursachenklärung von Thrombosen in den letzten fünf Jahren sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af74e0497056e9267fa3989830a45ff3
https://doi.org/10.1055/s-0038-1660383
https://doi.org/10.1055/s-0038-1660383
Publikováno v:
Hamostaseologie. 30(3)
A 17-year old man was sent to us for coagulation testing because he suffered from acute bleeding which started immediately after making an incision in the skin for a urological surgery. The patient had a history of mild bleeding symptoms (nose bleeds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ddd2d8904cfe67180296ce8ea976b1a
https://pubmed.ncbi.nlm.nih.gov/20680227
https://pubmed.ncbi.nlm.nih.gov/20680227
Publikováno v:
Hamostaseologie. 29(2)
A 14 year old boy was referred to us for a detailed coagulation study because a previously performed aPTT has been found prolonged. The boy had no history of bleeding symptoms and also the family history was negative for bleeding or thrombotic events
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9619425ee929f6f8abfb5c0f7076e9ae
https://pubmed.ncbi.nlm.nih.gov/19404525
https://pubmed.ncbi.nlm.nih.gov/19404525
Publikováno v:
37th Hemophilia Symposium ISBN: 9783540735342
Resistance to activated protein C (APC resistance) was identified as the cause of familial thrombophilia by Dahlback et al. in 1993 [4]. Only one year later the underlying genetic defect of the APC resistance has been demonstrated by Bertina and coll
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::88c9ae5951014f684a874176a5eb6fa6
https://doi.org/10.1007/978-3-540-73535-9_40
https://doi.org/10.1007/978-3-540-73535-9_40
Publikováno v:
36th Hemophilia Symposium Hamburg 2005 ISBN: 9783540367147
Among the hereditary thrombophilic states antithrombin deficiency is one of the most powerful factors. The disorder was first described in 1965 by Egeberg [6]. The pattern of inheritance of familiar antithrombin deficiency is autosomal-dominant, mean
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09e765250f99dec5597405ba48d60755
https://doi.org/10.1007/978-3-540-36715-4_37
https://doi.org/10.1007/978-3-540-36715-4_37
Publikováno v:
34th Hemophilia Symposium ISBN: 3540228861
The inherited Factor XI deficiency seems to be, with only few exceptions, a rare disorder worldwide. In patients with factor XI deficiency spontaneous bleedings are uncommon, bleeding events occur mostly after surgical procedures or injuries in perso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5975058de566f82e32ea57fc42cd717c
https://doi.org/10.1007/3-540-27022-1_25
https://doi.org/10.1007/3-540-27022-1_25