Zobrazeno 1 - 7
of 7
pro vyhledávání: '"C M, Millar"'
Autor:
C. L. Shovlin, C. M. Millar, F. Droege, A. Kjeldsen, G. Manfredi, P. Suppressa, S. Ugolini, N. Coote, A. D. Fialla, U. Geisthoff, G. M. Lenato, H. J. Mager, F. Pagella, M. C. Post, C. Sabbà, U. Sure, P. M. Torring, S. Dupuis-Girod, E. Buscarini, VASCERN-HHT
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-8 (2019)
Abstract Background Hereditary hemorrhagic telangiectasia (HHT) is a rare vascular dysplasia resulting in visceral arteriovenous malformations and smaller mucocutaneous telangiectasia. Most patients experience recurrent nosebleeds and become anemic w
Externí odkaz:
https://doaj.org/article/d71578396d96461388812ee10de55b6b
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(3)
Type 2B von Willebrand disease (VWD) is a rare, inherited bleeding disorder resulting from a qualitative defect in von Willebrand factor (VWF). There is very little published information on how to quantify bleeding risk and manage haemostasis in type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8bf4cbb90e3c5a013229f4c98140b47e
https://pubmed.ncbi.nlm.nih.gov/22077376
https://pubmed.ncbi.nlm.nih.gov/22077376
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
Autor:
C M, Millar, N, Connor, G, Dolan, C A, Lee, M, Makris, J, Wilde, M, Winter, J W, Ironside, N, Gill, F G H, Hill
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(2)
The appearance and rapid evolution of BSE in UK cattle in the mid 1980s, with compelling data supporting variant Creutzfeldt-Jakob disease (vCJD) as its human manifestation, pose a potentially severe threat to public health. Three clinical cases and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35df5e94c2c87fb4e6aa6f0a500d7b40
https://pubmed.ncbi.nlm.nih.gov/21362112
https://pubmed.ncbi.nlm.nih.gov/21362112
Autor:
A, Peden, L, McCardle, M W, Head, S, Love, H J T, Ward, S N, Cousens, D M, Keeling, C M, Millar, F G H, Hill, J W, Ironside
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 16(2)
All UK patients with bleeding disorders treated with any UK-sourced pooled factor concentrates between 1980 and 2001 have been informed that they may be at an increased risk of infection with variant Creutzfeldt-Jakob disease (vCJD). We describe a st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4c0a08c83ed73165cfb0f600ee1f1da
https://pubmed.ncbi.nlm.nih.gov/20070383
https://pubmed.ncbi.nlm.nih.gov/20070383
Publikováno v:
Haemophilia. 14:1131-1132
We read with interest the comprehensive National Heart, Lung, and Blood Institute (NHLBI) guidelines for the diagnosis and management of von Willebrand disease (VWD) [1]. However, we would like to draw attention to a practically important diagnostic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16310ed83192e013eba168a1aabd0b09
https://doi.org/10.1111/j.1365-2516.2008.01818.x
https://doi.org/10.1111/j.1365-2516.2008.01818.x
Publikováno v:
British Journal of Haematology. 130:462-463
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e424eb690fcbe8e49d941bb06acce6d1
https://doi.org/10.1111/j.1365-2141.2005.05637.x
https://doi.org/10.1111/j.1365-2141.2005.05637.x