Rare bleeding disorders
dc.contributor.author | Peyvandi, F. | en_US |
dc.contributor.author | Kaufman, R. J. | en_US |
dc.contributor.author | Seligsohn, U. | en_US |
dc.contributor.author | Salomon, O. | en_US |
dc.contributor.author | Bolton-Maggs, P. H. B. | en_US |
dc.contributor.author | Spreafico, M. | en_US |
dc.contributor.author | Menegatti, M. | en_US |
dc.contributor.author | Palla, R. | en_US |
dc.contributor.author | Siboni, S. | en_US |
dc.contributor.author | Mannucci, P. M. | en_US |
dc.date.accessioned | 2010-06-01T18:28:41Z | |
dc.date.available | 2010-06-01T18:28:41Z | |
dc.date.issued | 2006-07 | en_US |
dc.identifier.citation | PEYVANDI, F.; KAUFMAN, R. J.; SELIGSOHN, U.; SALOMON, O.; BOLTON-MAGGS, P. H. B.; SPREAFICO, M.; MENEGATTI, M.; PALLA, R.; SIBONI, S.; MANNUCCI, P. M. (2006). "Rare bleeding disorders." Haemophilia 12(s3): 137-142. <http://hdl.handle.net/2027.42/71685> | en_US |
dc.identifier.issn | 1351-8216 | en_US |
dc.identifier.issn | 1365-2516 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/71685 | |
dc.identifier.uri | http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=16684009&dopt=citation | en_US |
dc.format.extent | 121933 bytes | |
dc.format.extent | 3109 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.publisher | Blackwell Publishing Ltd | en_US |
dc.rights | 2006 The Authors Journal compilation 2006 Blackwell Publishing Ltd | en_US |
dc.subject.other | Rare Bleeding Disorders | en_US |
dc.subject.other | RBDs | en_US |
dc.subject.other | Genetics | en_US |
dc.subject.other | Treatment | en_US |
dc.subject.other | Guidelines | en_US |
dc.subject.other | International Registry of RBDs | en_US |
dc.subject.other | RBDD | en_US |
dc.title | Rare bleeding disorders | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Oncology and Hematology | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationother | * Department of Medicine and Medical Specialities, IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, University of Milan, Milan, Italy | en_US |
dc.contributor.affiliationother | Department of Biological Chemistry, Howard Hughes Medical Institute, University of Michigam Medical Center, Ann Arbor, MI, USA | en_US |
dc.contributor.affiliationother | The Amalia Biron Research Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel Hashomer and Sackler Faculty of Medicine, Tel Aviv University, Israel | en_US |
dc.contributor.affiliationother | Department of Clinical Haematology, Manchester Royal Infirmary, Manchester, UK | en_US |
dc.contributor.affiliationother | Department of Medicine and Medical Specialities, IRCCS Maggiore Hospital, Mangiagalli and Regina Elena Foundation, Univeristy of Milan, Milan, Italy. | en_US |
dc.identifier.pmid | 16684009 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/71685/1/j.1365-2516.2006.01271.x.pdf | |
dc.identifier.doi | 10.1111/j.1365-2516.2006.01271.x | en_US |
dc.identifier.source | Haemophilia | en_US |
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dc.identifier.citedreference | Salomon O, Steinberg DM, Seligsohn U. Variable bleeding manifestation during different types of surgery in patients with severe factor XI deficiency support tailored replacement therapy. Submitted for publication 2006. | en_US |
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dc.identifier.citedreference | 11 Clinical Practice Guideline No. 1: acute pain management: operative or medical procedures and trauma. Rockville (MD): US Department of Health and Human Services. Agency for Health Care Policy and Research; 1993. AHCPR Publication No. 92–0023. [cited 1993] | en_US |
dc.identifier.citedreference | Bolton-Maggs PH, Perry DJ, Chalmers EA et al. The rare coagulation disorders – review with guidelines for management from the United Kingdom Haemophilia Centre Doctors’ Organisation. Haemophilia 2004; 10: 593 – 628. | en_US |
dc.identifier.citedreference | Acharya S et al. Rare bleeding disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias. J Thromb Haemost 2004; 2: 248 – 56. | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
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