Results 41 to 50 of about 22,562,840 (346)

Randomized trial of a DVD intervention to improve readiness to self-manage joint pain [PDF]

, 2011
Report of a randomized controlled trial of a motivational intervention to promote self-management of joint painA DVD (digital video disk) intervention to increase readiness to self-manage joint pain secondary to hemophilia was informed by a 2-phase ...
Abraham, Altman, Angst, Barlow, Barlow, Barry, Biller, Bode, Carr, Choiniere, Dijkstra, Elander, Elander, Elander, Fischer, Glenn, Habib, Hadjistavropoulos, Hays, Hays, Heapy, Jensen, Jensen, Jensen, Jensen, Kazis, Kerns, Kerns, Kerns, LeFort, Liao, Luck, McCracken, Moore, Nielsen, Prochaska, Richmond, Ruta, Szende, Turk, Turk, Von Korff, Vowles, Warsi   +43 more
core   +2 more sources

Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia

The Application of Clinical Genetics, 2022
Ampaiwan Chuansumrit,1 Werasak Sasanakul,1 Nongnuch Sirachainan,1 Suttikarn Santiwatana,1 Praguywan Kadegasem,1 Pakawan Wongwerawattanakoon,2 Noppawan Tungbubpha,1 Juthamard Chantaraamporn1 1Department of Pediatrics, Faculty of Medicine, Ramathibodi ...
Chuansumrit A, Sasanakul W, Sirachainan N, Santiwatana S, Kadegasem P, Wongwerawattanakoon P, Tungbubpha N, Chantaraamporn J   +7 more
doaj  

Designing ATHN 7: Safety, effectiveness and practice of treatment of people with haemophilia in the United States through a natural history cohort study

The Journal of Haemophilia Practice, 2023
Haemophilia A and B are X-linked inherited bleeding disorders, resulting in the deficiency of clotting factor VIII and IX, respectively. Since the introduction of recombinant clotting factor concentrates in the early 1990s, the major safety concern for ...
Buckner Tyler W., Daoud Nabil, Miles Moses, O'Neill Carrie, Watson Crystal, Recht Michael   +5 more
doaj   +1 more source

Haemophilia item bank based on International Classification of Functioning, Disability and Health: a systematic review

Hematology, 2023
Background and Objectives Haemophilia comprises a continuum of blood disorders that often include joint and muscular dysfunction, which may lead to a constellation of activity limitations and participation restrictions.
Bao-Feng Geng, Chun Feng, Shou-Guo Liu, Zhong-Li Jiang, Feng Lin   +4 more
doaj   +1 more source

Recombinant factorVIII Fc fusion protein for the prevention and treatment of bleeding in children with severe hemophilia A [PDF]

, 2015
This work was supported by funding from Biogen, including funding for the editorial and writing support in the the development of this ...
Allen, G, Barnes, C, Cristiano, LM, Gambino, G, Kulkarni, R, Liesner, R, Mahlangu, J, Neelakantan, S, Nolan, B, Pasi, J, Pierce, GF, Young, G   +11 more
core   +1 more source

Molecular Profiling of FIX (FACTOR 9) Gene of Hemophilia B in Karnataka

BLDE University Journal of Health Sciences, 2020
Introduction: Haemophilia is one of the “Bleeder Disorder” that causes abnormal bleeding or poor blood clotting. It occurs due to the defect in the clotting factors even in their functions and in some cases structures are altered.
Sujayendra Kulkarni, Rajat Hegde, Smita Hegde, Suyamindra Kulkarni, Sanjeev Kolagi, Pramod Gai, Rudragouda Bulagouda   +6 more
doaj   +1 more source

The Second Team Haemophilia Education Meeting, 2016, Frankfurt, Germany [PDF]

, 2017
The first Team Haemophilia Education (THE) Meeting was held on 7-8 May 2015 in Amsterdam, The Netherlands. It aimed to promote the optimal care of patients with haemophilia through education of the multidisciplinary treatment team.
Berntorp, E, Blatný, J, Chambost, H, d'Oiron, R, Dargaud, Y, Dettoraki, A, Doria, AS, Farrell, A, Halimeh, S, Hart, D, Holme, PA, Kaczmarek, R, Laane, E, Lobet, S, Maia, R, Mancuso, ME, Mantovani, L, McLaughlin, P, Nanayakkara, L, Perry, D, Petrini, P, Pollard, D, Raza, S, Sannié, T, Taylor, S, van den Berg, M   +25 more
core   +1 more source

''Sickle cell trait and haemophilia: a rare association''

The Pan African Medical Journal, 2018
In this paper we analyze the combination of HbAS disease and haemophilia A must be exceedingly rare. Because of this rarity we report the case of two brothers with sickle cell trait and major haemophilia A.
Hayat El Maataoui, Amina Fahi, Bouchra Oukkache   +2 more
doaj   +1 more source

Successful elimination of factor VIII inhibitor using cyclosporin A [PDF]

, 2003
No abstract ...
Dykes, Gordon D. O. Lowe, Grunewald, Hay, Isobel D. Walker, Lian, Mark D. McColl, Morrison, Peter S. Maclean, Pfliegler, R. Campbell Tait   +10 more
core   +1 more source

Atypical Presenting Symptoms of Acute Onset Acquired Haemophilia with Eosinophilic Fasciitis

European Journal of Case Reports in Internal Medicine, 2020
Acquired haemophilia is a bleeding disorder caused by antibodies against coagulation factors. Some cases are associated with autoimmune diseases. However, no cases of acquired haemophilia with eosinophilic fasciitis have been previously reported.
Yuto Nakakubo, Kazuyo Yamamoto, Masaaki Fujita   +2 more
doaj   +1 more source