341 related articles for article (PubMed ID: 21689212)
1. Haemophilia utilization group study - Part Va (HUGS Va): design, methods and baseline data.
Zhou ZY; Wu J; Baker J; Curtis R; Forsberg A; Huszti H; Koerper M; Lou M; Miller R; Parish K; Riske B; Shapiro A; Ullman M; Johnson K
Haemophilia; 2011 Sep; 17(5):729-36. PubMed ID: 21689212
[TBL] [Abstract][Full Text] [Related]
2. Quality of life in haemophilia A: Hemophilia Utilization Group Study Va (HUGS-Va).
Poon JL; Zhou ZY; Doctor JN; Wu J; Ullman MM; Ross C; Riske B; Parish KL; Lou M; Koerper MA; Gwadry-Sridhar F; Forsberg AD; Curtis RG; Johnson KA
Haemophilia; 2012 Sep; 18(5):699-707. PubMed ID: 22507546
[TBL] [Abstract][Full Text] [Related]
3. Utilization of care in haemophilia: a resource-based method for cost analysis from the Haemophilia Utilization Group Study (HUGS).
Globe DR; Curtis RG; Koerper MA;
Haemophilia; 2004 Mar; 10 Suppl 1():63-70. PubMed ID: 14987251
[TBL] [Abstract][Full Text] [Related]
4. Healthcare resource utilization among haemophilia A patients in the United States.
Valentino LA; Pipe SW; Tarantino MD; Ye X; Xiong Y; Luo MP
Haemophilia; 2012 May; 18(3):332-8. PubMed ID: 22044662
[TBL] [Abstract][Full Text] [Related]
5. Self-reported barriers to hemophilia care in people with factor VIII deficiency.
Zhou ZY; Riske B; Forsberg AD; Ullman M; Baker JR; Koerper MA; Curtis RG; Lou M; Joanne W; Johnson KA
Am J Prev Med; 2011 Dec; 41(6 Suppl 4):S346-53. PubMed ID: 22099357
[TBL] [Abstract][Full Text] [Related]
6. Retrospective analysis of differences in annual factor VIII utilization among haemophilia A patients.
Epstein J; Xiong Y; Woo P; Li-McLeod J; Spotts G
Haemophilia; 2012 Mar; 18(2):187-92. PubMed ID: 21883704
[TBL] [Abstract][Full Text] [Related]
7. Factor VIII prophylaxis for adult patients with severe haemophilia A: results of a US survey of attitudes and practices.
Walsh CE; Valentino LA
Haemophilia; 2009 Sep; 15(5):1014-21. PubMed ID: 19493018
[TBL] [Abstract][Full Text] [Related]
8. Haemophilia care in Europe: the ESCHQoL study.
Schramm W; Gringeri A; Ljung R; Berger K; Crispin A; Bullinger M; Giangrande PL; Von Mackensen S; Mantovani LG; Nemes L; Serban M;
Haemophilia; 2012 Sep; 18(5):729-37. PubMed ID: 22639833
[TBL] [Abstract][Full Text] [Related]
9. Burden of illness: direct and indirect costs among persons with hemophilia A in the United States.
Zhou ZY; Koerper MA; Johnson KA; Riske B; Baker JR; Ullman M; Curtis RG; Poon JL; Lou M; Nichol MB
J Med Econ; 2015 Jun; 18(6):457-65. PubMed ID: 25660324
[TBL] [Abstract][Full Text] [Related]
10. US Hemophilia Treatment Center population trends 1990-2010: patient diagnoses, demographics, health services utilization.
Baker JR; Riske B; Drake JH; Forsberg AD; Atwood R; Voutsis M; Shearer R
Haemophilia; 2013 Jan; 19(1):21-6. PubMed ID: 22845803
[TBL] [Abstract][Full Text] [Related]
11. A profile of children with disabilities receiving SSI: highlights from the National Survey of SSI Children and Families.
Rupp K; Davies PS; Newcomb C; Iams H; Becker C; Mulpuru S; Ressler S; Romig K; Miller B
Soc Secur Bull; 2005-2006; 66(2):21-48. PubMed ID: 16878426
[TBL] [Abstract][Full Text] [Related]
12. Protease inhibitor combination therapy, severity of illness, and quality of life among children with perinatally acquired HIV-1 infection.
Storm DS; Boland MG; Gortmaker SL; He Y; Skurnick J; Howland L; Oleske JM;
Pediatrics; 2005 Feb; 115(2):e173-82. PubMed ID: 15629958
[TBL] [Abstract][Full Text] [Related]
13. A haemophilia treatment centre-administered disease management programme in patients with bleeding disorders.
Tencer T; Roberson C; Duncan N; Johnson K; Shapiro A
Haemophilia; 2007 Sep; 13(5):480-8. PubMed ID: 17880433
[TBL] [Abstract][Full Text] [Related]
14. The relative burden of haemophilia A and the impact of target joint development on health-related quality of life: results from the ADVATE Post-Authorization Safety Surveillance (PASS) study.
Klamroth R; Pollmann H; Hermans C; Faradji A; Yarlas AS; Epstein JD; Ewenstein BM
Haemophilia; 2011 May; 17(3):412-21. PubMed ID: 21332888
[TBL] [Abstract][Full Text] [Related]
15. Cross-cultural development and psychometric evaluation of a patient-reported health-related quality of life questionnaire for adults with haemophilia.
Rentz A; Flood E; Altisent C; Bullinger M; Klamroth R; Garrido RP; Scharrer I; Schramm W; Gorina E;
Haemophilia; 2008 Sep; 14(5):1023-34. PubMed ID: 18665853
[TBL] [Abstract][Full Text] [Related]
16. Children with special health care needs enrolled in the State Children's Health Insurance Program (SCHIP): patient characteristics and health care needs.
Szilagyi PG; Shenkman E; Brach C; LaClair BJ; Swigonski N; Dick A; Shone LP; Schaffer VA; Col JF; Eckert G; Klein JD; Lewit EM
Pediatrics; 2003 Dec; 112(6 Pt 2):e508. PubMed ID: 14654673
[TBL] [Abstract][Full Text] [Related]
17. Disability in Indian patients with haemophilia.
Kar A; Mirkazemi R; Singh P; Potnis-Lele M; Lohade S; Lalwani A; Saha AS
Haemophilia; 2007 Jul; 13(4):398-404. PubMed ID: 17610556
[TBL] [Abstract][Full Text] [Related]
18. Haemophilia Utilization Group Study: assessment of functional health status in haemophilia.
Globe DR; Cunningham WE; Andersen R; Dietrich SL; Curtis RG; Parish KL; Miller RT; Sanders NL; Kominski G
Haemophilia; 2002 Mar; 8(2):121-8. PubMed ID: 11952847
[TBL] [Abstract][Full Text] [Related]
19. Changing factors and changing needs in women's health care.
Leslie LA; Swider SM
Nurs Clin North Am; 1986 Mar; 21(1):111-23. PubMed ID: 3513129
[TBL] [Abstract][Full Text] [Related]
20. Quality of life, psychosocial strains and coping in parents of children with haemophilia.
Wiedebusch S; Pollmann H; Siegmund B; Muthny FA
Haemophilia; 2008 Sep; 14(5):1014-22. PubMed ID: 18624702
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
