Zobrazeno 1 - 10
of 57
pro vyhledávání: '"clotting factor deficiency"'
Autor:
Dandan Yu, Feng Xue, Xiaofan Liu, Yunfei Chen, Rongfeng Fu, Ting Sun, Xinyue Dai, Mankai Ju, Huan Dong, Renchi Yang, Wei Liu, Lei Zhang
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 8, Iss 6, Pp 102554- (2024)
Background: Isolated acquired clotting factor deficiencies (ACFDs) are mainly caused by the existence of anti-factor antibodies or adsorption of clotting factors onto substances such as amyloid. Besides acquired factor (F)VIII deficiency (acquired he
Externí odkaz:
https://doaj.org/article/967e6b8beb8e4256bbedac645847ba3b
Akademický článek
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Akademický článek
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Autor:
Maria Effrosyni Livanou, Alkis Matsas, Serena Valsami, Dimitrios T. Papadimitriou, Athanasios Kontogiannis, Panagiotis Christopoulos
Publikováno v:
Life, Vol 13, Iss 6, p 1321 (2023)
Clotting Factor deficiencies are rare disorders with variations in clinical presentation and severity of symptoms ranging from asymptomatic to mild to life-threatening bleeding. Thus, they pose a diagnostic and therapeutic challenge, mainly for the p
Externí odkaz:
https://doaj.org/article/c2896cfe12b44f58be367e49310dc49c
Akademický článek
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Publikováno v:
Journal of Pediatric Critical Care, Vol 5, Iss 3, Pp 94-97 (2018)
Factor X deficiency is one of the rare inherited coagulation disorders. Symptoms vary from mild to severe with the commonest being epistaxis, gum bleeds and menorrhagia. The diagnosis is suspected when both PT and aPTT are prolonged and remains uncor
Externí odkaz:
https://doaj.org/article/31a4c41290d3477198571167ddb51317
Autor:
M. A. Ovsiannikova, L. M. Makarova, Yu. I. Kucherov, Natalia V. Kholodnova, Yu. V. Zhirkova, M. B. Samorokovskaya, S. R. Adleiba, A. L. Belaya
Publikováno v:
Russian Journal of Pediatric Surgery. 23:276-280
The article describes two cases of children operated on for the biliary atresia (BA) on days 56 and 33 of their life. One child after the Kasai surgery had liver transplantation at the age of 1 year and 2 months because of the deterioration of his li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2c8f4cf68acf32286ff69b21b264776d
https://doi.org/10.18821/1560-9510-2019-23-5-276-280
https://doi.org/10.18821/1560-9510-2019-23-5-276-280
Autor:
ON Pierre-Louis, J Véronique-Baudin, J Rabout, MN Yerro, S Molcard, P Fuseau, M Vestris, G Aurokiom, J Smith-Ravin, C Joachim-Contaret, MS Pierre-Louis
Publikováno v:
WIMJ Open, Vol 5, Iss 2, Pp 47-51 (2018)
Objective: Haemophilia is a congenital bleeding disorder characterized by partial or complete deficiency of a clotting factor VIII (FVIII) for Haemophilia A (HA), or factor IX (FIX) for Haemophilia B (HB). In this study, we describe the epidemiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::7e36d938d21338c35d8d705fde5a6843
https://www.mona.uwi.edu/wimjopen/article/11773
https://www.mona.uwi.edu/wimjopen/article/11773
Publikováno v:
Journal of Pediatric Critical Care, Vol 5, Iss 3, Pp 94-97 (2018)
Factor X deficiency is one of the rare inherited coagulation disorders. Symptoms vary from mild to severe with the commonest being epistaxis, gum bleeds and menorrhagia. The diagnosis is suspected when both PT and aPTT are prolonged and remains uncor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee191bbae49b7858d966120316d7ed35
http://www.jpcc.org.in/article.asp?issn=2349-6592
http://www.jpcc.org.in/article.asp?issn=2349-6592
Autor:
Simona Raso, Catherine Lambert, Cedric Hermans, Sergio Siragusa, A. Boban, Mariasanta Napolitano
Publikováno v:
Haemophilia, Vol. 26, no. 1, p. 117-121 (2020)
Introduction Certain haemophilia carriers demonstrate an increased bleeding tendency, mainly related to clotting factor deficiency. No study has so far formally compared the bleeding phenotype of women and girls with mild FVIII or FIX deficiency and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc5310602b1079808e81830845b78a69
https://pubmed.ncbi.nlm.nih.gov/31815335
https://pubmed.ncbi.nlm.nih.gov/31815335