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haemophilia

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Book Chapter
Published: 09 February 1996
10.1159/000425374
EISBN: 978-3-318-04771-4
... Abstract One of the most serious complications of the treatment of haemophilia A is the development of inhibitors. Former studies mostly considered the prevalence of inhibitor development, thus underestimating its true risk. Prevalences ranged widely (7–18%) probably due to the populations...
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Book Chapter
Series: Current Studies in Hematology and Blood Transfusion
Volume: 34
Published: 08 December 1969
10.1159/000384904
EISBN: 978-3-318-03503-2
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Book Chapter
Published: 20 June 2013
10.1159/000346924
EISBN: 978-3-318-02198-1
...: DDAVP responsiveness in children with mild or moderate haemophilia A correlates with age, endogenous FVIII:C level and with haemophilic genotype. Haemophilia 2012;18:50-55 3. Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, et al: Guidelines for the management...
Book Chapter
Published: 20 June 2013
EISBN: 978-3-318-02198-1
...: DDAVP responsiveness in children with mild or moderate haemophilia A correlates with age, endogenous FVIII:C level and with haemophilic genotype. Haemophilia 2012;18:50-55 3. Srivastava A, Brewer AK, Mauser-Bunschoten EP, Key NS, Kitchen S, Llinas A, et al: Guidelines for the management...
Book Chapter
Published: 20 June 2013
10.1159/000346947
EISBN: 978-3-318-02198-1
... 2013;60:(suppl 1)S37-S40 3. Peyvandi F, Bolton-Maggs PH, Batorova A, De Moerloose P: Rare bleeding disorders. Haemophilia 2012;18:(suppl 4)148-153 4. Seligsohn U: Factor XI deficiency in humans. J Thromb Haemost 2009;7:(suppl 1)84-87 5. Emsley J, McEwan PA, Gailani D: Structure and function...
Book Chapter
Published: 20 June 2013
EISBN: 978-3-318-02198-1
... 2013;60:(suppl 1)S37-S40 3. Peyvandi F, Bolton-Maggs PH, Batorova A, De Moerloose P: Rare bleeding disorders. Haemophilia 2012;18:(suppl 4)148-153 4. Seligsohn U: Factor XI deficiency in humans. J Thromb Haemost 2009;7:(suppl 1)84-87 5. Emsley J, McEwan PA, Gailani D: Structure and function...
Book Chapter
Published: 20 June 2013
10.1159/000346923
EISBN: 978-3-318-02198-1
...References References 1. Bolton-Maggs PH, Lillicrap D, Goudemand J, Berntorp E: von Willebrand disease update: diagnostic and treatment dilemmas. Haemophilia 2008;14:(suppl 3)56-61 2. Lillicrap D: The basic science, diagnosis and clinical management of von Willebrand disease. Treatment...
Book Chapter
Published: 20 June 2013
EISBN: 978-3-318-02198-1
...References References 1. Bolton-Maggs PH, Lillicrap D, Goudemand J, Berntorp E: von Willebrand disease update: diagnostic and treatment dilemmas. Haemophilia 2008;14:(suppl 3)56-61 2. Lillicrap D: The basic science, diagnosis and clinical management of von Willebrand disease. Treatment...
Book Chapter
Series: Pediatric and Adolescent Medicine
Volume: 17
Published: 29 November 2013
EISBN: 978-3-318-02423-4
...://www.dh.gov.uk/prod_consum_dh/groups/dh_digitalassets/documents/digitalasset/dh_127632.pdf 2011. 21. Breakey VR, Blanchette VS, Bolton-Maggs PH: Towards comprehensive care in transition for young people with haemophilia. Haemophilia 2010;16:848-857. 22. Khair K, Gibson F, Meerabeau L: The benefits...
Book Chapter
Series: Pediatric and Adolescent Medicine
Volume: 17
Published: 29 November 2013
10.1159/000350353
EISBN: 978-3-318-02423-4
... or lifelong conditions such as haemoglobin disorders or haemophilia will need to make the transition, which will frequently mean not only a change in medical personnel whom they have known perhaps since early childhood, but also to a different clinical environment or a different hospital. It is notable...