National needs assessment of patients treated at the United States Federally-Funded Hemophilia Treatment Centers.

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Understanding stakeholder important outcomes and perceptions of equity, acceptability and feasibility of a care model for haemophilia management in the US: a qualitative study.A gap in comprehensive care: Sexual health in men with haemophilia.

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National needs assessment of patients treated at the United States Federally-Funded Hemophilia Treatment Centers.

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2015 nî lūn-bûn

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P2860

The universal data collection surveillance system for rare bleeding disorders.

Physical and psychosocial challenges in adult hemophilia patients with inhibitors.

Advances in care of children with hemophilia.

Models for psychosocial services in the developed and developing world.

Healthcare expenditures for males with haemophilia and employer-sponsored insurance in the United States, 2008.

Meeting the emerging public health needs of persons with blood disorders.

Infectious disease in the blood supply and the public health response.

Towards comprehensive care in transition for young people with haemophilia.

Confronting the psychological burden of haemophilia.

Psychosocial aspects of haemophilia: a systematic review of methodologies and findings.

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10.1111/HAE.12810

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hemophilia

Ameeriga Ütisriigiq

National needs assessment of patients treated at the United States Federally-Funded Hemophilia Treatment Centers.

about

P2860

P2860

National needs assessment of patients treated at the United States Federally-Funded Hemophilia Treatment Centers.

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