Zobrazeno 1 - 10
of 36
pro vyhledávání: '"J. T. Wilde"'
Publikováno v:
Haemophilia. 18:685-687
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9478a33c0fb9e031b8da9cbeb741937
https://doi.org/10.1111/j.1365-2516.2012.02801.x
https://doi.org/10.1111/j.1365-2516.2012.02801.x
Publikováno v:
Gut. 46:534-539
BACKGROUND—Hereditary deficiencies of natural anticoagulant proteins are implicated in the pathogenesis of portal vein thrombosis (PVT). Secondary deficiencies of these proteins have also been reported in PVT, making interpretation of concentration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f09641e3003074940b54ac38491ff7b4
https://doi.org/10.1136/gut.46.4.534
https://doi.org/10.1136/gut.46.4.534
Publikováno v:
The Journal of Laryngology & Otology. 113:924-927
Haemophilic pseudotumour or haemophilic cyst is a rare complication of haemophilia, occurring in one to two per cent of individuals with a severe factor VIII or IX deficiency. We report a case of a haemophilic pseudotumour in a hitherto unreported si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9339d08f7843464bd94d2edb5a6d5b5f
https://doi.org/10.1017/s002221510014561x
https://doi.org/10.1017/s002221510014561x
Publikováno v:
British Journal of Haematology. 106:427-430
We describe an enzyme-linked immunosorbent assay (ELISA) based primer extension method for the detection of the factor V Leiden (FVL) mutation. The wild-type nucleotide at position 1691 or the mutant nucleotide at the complementary position on the an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::794f95e9d2bdfb15c90d3ac74c00bb57
https://doi.org/10.1046/j.1365-2141.1999.01536.x
https://doi.org/10.1046/j.1365-2141.1999.01536.x
Publikováno v:
Sexually Transmitted Infections. 74:439-444
Case report (Dr A Winter) A Peruvian man in his 30s was admitted as an emergency with a 3 week history of fluctuating temperatures and rigors, a worsening sore throat, and a 4 day history of non-bloody diarrhoea without significant abdominal pain. On
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96e4cebbf509096e5e8ee77ae9a78c45
https://doi.org/10.1136/sti.74.6.439
https://doi.org/10.1136/sti.74.6.439
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b601c1b4e2190b1570641c33814d7ebb
https://pubmed.ncbi.nlm.nih.gov/22925332
https://pubmed.ncbi.nlm.nih.gov/22925332
The UK Haemophilia Doctors Organisation triennial audit of UK Comprehensive Care Haemophilia Centres
Autor:
J T, Wilde
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(4)
Under the auspices of the United Kingdom Haemophilia Doctors Organisation (UKHCDO) the UK Comprehensive Care Haemophilia Centres (CCCs) have undergone a three yearly formal audit assessment since 1993. This report describes the evolution of the audit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::babd79b96492404894f4d3fd61c48a81
https://pubmed.ncbi.nlm.nih.gov/22564196
https://pubmed.ncbi.nlm.nih.gov/22564196
Publikováno v:
Journal of Obstetrics and Gynaecology. 14:193-196
SummarySummaryProthrombin fragment F1 + 2 and thrombin-antithrombin complexes (TAT) were measured in 97 postmenopausal women, either untreated or stabilised on subcutaneous depot, oral or transdermal hormone replacement treatment. Thirty-two used dep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32846d77888d90837ecbd6f30cd4913c
https://doi.org/10.3109/01443619409004074
https://doi.org/10.3109/01443619409004074
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17(5)
Chronic HCV infection continues to be of significant clinical importance in patients with hereditary bleeding disorders. This guideline provides information on the recent advances in the investigation and treatment of HCV infection and gives GRADE sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7c1661ceb7369e57404b52f711acbabb
https://pubmed.ncbi.nlm.nih.gov/21658165
https://pubmed.ncbi.nlm.nih.gov/21658165
Autor:
S M A, Zaman, F G H, Hill, B, Palmer, C M, Millar, A, Bone, A M, Molesworth, N, Connor, C A, Lee, G, Dolan, J T, Wilde, O N, Gill, M, Makris
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 17(6)
The risk of variant Creutzfeldt-Jakob disease (vCJD) from potentially infected plasma products remains unquantified. This risk has been assessed for 787 UK patients with an inherited bleeding disorder prospectively followed-up for 10-20 years through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58caf53d42fa822f15ba8fdff5c6835c
https://pubmed.ncbi.nlm.nih.gov/21342369
https://pubmed.ncbi.nlm.nih.gov/21342369