- ►annals.org M Triemstra, FR Rosendaal, C Smit, HM Van … - Annals of internal medicine, 1995 - Am Coll Physicians Add to CiteULike Add to Complore Add to Connotea Add to Del.icio.us Add to Digg
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Objective: To determine causes of death and mortality rates in patients ... Cited by 77 - Related articles - All 4 versions
FR Rosendaal, I Varekamp, C Smit, AH … - Br J Haematol, 1989 - interscience.wiley.com Mortality figures were calculated for a group of 717 Dutch haemophiliacs over
the period 1973-86. Follow-up was on average 10.9 years; no patients were lost
to follow-up. The data were compared to the general male population by ... Cited by 86 - Related articles - All 3 versions
FR Rosendaal, E Briet, J Stibbe, G Van … - British journal of haematology, 1990 - ncbi.nlm.nih.gov We previously reported that mortality due to ischaemic heart disease was lower
in haemophilia patients than in the general male population. To support the
hypothesis that this could be attributed to a protective effect of the ... Cited by 69 - Related articles - All 2 versions
TL Chorba, RC Holman, TW Strine, MJ Clarke, … - American journal of hematology, 1994 - interscience.wiley.com To examine recent changes in longevity and the causes of death among persons
with hemophilia A, we evaluated death certificate data for persons who died in
the United States from 1968 through 1989 and had hemophilia A or congenital ... Cited by 46 - Related articles - BL Direct - All 4 versions
IR Walker, JA Julian - Haemophilia, 1998 - ingentaconnect.com The life expectancy of individuals with haemophilia was close to that of the
general population in the early 1980s. Since then, life expectancy has
decreased, due to transfusion-transmitted virus infections. Deaths in ... Cited by 26 - Related articles - BL Direct - All 3 versions
- ►nih.gov [PDF] C Smit, FR Rosendaal, I Varekamp, A Brocker- … - British Medical Journal, 1989 - bmj.com Page 1. doi:10.1136/bmj.298.6668.235 1989;298;235-238 BMJ P. Suurmeijer and E. Briët
C. Smit, FR Rosendaal, I. Varekamp, A. Bröcker-Vriends, H. Van Dijck, T. ... Cited by 27 - Related articles - All 6 versions
- ►ahajournals.org A Sramek, JHC Reiber, WBJ Gerrits, FR … - Circulation, 2001 - Am Heart Assoc Methods and Results— A total of 76 individuals with an inherited bleeding
tendency (hemophilia and von Willebrand disease) and 142 healthy controls were
included in the present study. Early atherosclerotic vessel-wall changes ... Cited by 38 - Related articles - BL Direct - All 9 versions
SA Larsson, B Wiechel - Acta Medica Scandinavica, 1983 - ncbi.nlm.nih.gov One hundred and eighteen patients with hemophilia A or B died in Sweden between
1957 and 1980. The causes and circumstances of death have been the subject of a
retrospective study. The most striking feature was the increase in age at ... Cited by 39 - Related articles - All 2 versions
E Ikkala, T Helske, HRN MYLLYLA, P … - British Journal of Huernutology, 1982 - interscience.wiley.com Summary. Important advances have been made in the treatment of haemophilia
during the past 30 years. We have analysed the data of all the known 163
patients with severe haemophilia A living in Finland in 1930–79 in order ... Cited by 39 - Related articles - All 2 versions
SA Larsson - British journal of haematology, 1985 - ncbi.nlm.nih.gov Life expectancy of Swedish haemophiliacs has been estimated for the period
1831-1980. The data were derived from 948 haemophiliacs of whom 580 survived
throughout 1980. Applying standard demographic techniques, median life ... Cited by 72 - Related articles - All 2 versions
