Zobrazeno 1 - 10
of 142
pro vyhledávání: '"B. Maak"'
Autor:
K. B. Gbaranor, E. E. Ben, T. H. Olatunbosun, B. Maakai, B. M. Otobo, E. T. Godam, K. S. Enebeli, F. Saronee, N. D. Etim, B. Z. Ovili-Odili
Publikováno v:
Journal of Applied Sciences and Environmental Management, Vol 28, Iss 11 (2024)
This paper evaluates the effects of hydro-alcohol extract of Englerina drummomdii Balla ex Polhil & Wiens leaves on the histology of ovaries and uterine tissues of female Wistar rats using appropriate standard methods with forty-nine (49) Wistar rats
Externí odkaz:
https://doaj.org/article/aa365f71a6f94a3f91055d6e9854761b
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
Autor:
Annelie Siegemund, Heidrun Rühling, Winnie Schröder, Karin Wulff, B. Maak, U. Budde, Falko H. Herrmann
Publikováno v:
Monatsschrift Kinderheilkunde. 147:104-109
Eine junge Frau mit verstarkten Regelblutungen und langer anhaltenden Blutungen aus nur geringgradigen Verletzungen wurde untersucht, wobei eine sehr stark verlangerte PTT ( >200 s) auffiel. Die Messung der Faktor-XII-Aktivitat ergab mit weniger als
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d1fcb6527d920fd2a8d43a7306de069
https://doi.org/10.1007/s001120050405
https://doi.org/10.1007/s001120050405
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:
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:
Transfusion medicine (Oxford, England). 16(2)
summary. Neonatal alloimmune thrombocytopenia (NAIT) occurs when maternal alloantibodies to antigens presented on foetal platelets cause their immune destruction. Whether human leucocyte antigen (HLA) antibodies can cause NAIT is controversial. Here,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89d38ed0f082f03ba07cac54651ae490
https://pubmed.ncbi.nlm.nih.gov/16623921
https://pubmed.ncbi.nlm.nih.gov/16623921
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
Publikováno v:
32nd Hemophilia Symposium Hamburg 2001 ISBN: 9783540438847
Today we have certain knowledge about a number of hereditary factors which change the hemostatic balance of their carriers towards a tendency to develop venous thrombo-embolism. Typically the first Manifestation occurs frequently without any recogniz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c91bccca87e70e3603c7620514dd0114
https://doi.org/10.1007/978-3-642-18150-4_23
https://doi.org/10.1007/978-3-642-18150-4_23
Publikováno v:
32nd Hemophilia Symposium Hamburg 2001 ISBN: 9783540438847
In 1953, Rosenthal et al. [14] described a new hemophilia-like bleeding disorder. In contrast to the true hemophilias, the newly detected coagulation defect was present in Males and females. Moreover, in Mixing experiments the observed defect could b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e709b11cefb25e5f44c81143b438e76a
https://doi.org/10.1007/978-3-642-18150-4_33
https://doi.org/10.1007/978-3-642-18150-4_33