A Cross-National Survey of People Living with Hemophilia: Impact on Daily Living and Patient Education in Central Europe-Reference-Cited by-同舟云学术

A Cross-National Survey of People Living with Hemophilia: Impact on Daily Living and Patient Education in Central Europe

Published:2021-04 Issue: Volume:Volume 15 Page:871-883
ISSN:1177-889X
Container-title:Patient Preference and Adherence
language:en
Short-container-title:PPA

Author:

Banchev Atanas^ORCID,Batorova Angelika,Faganel Kotnik Barbara,Kiss Csongor,Puras Gediminas,Zapotocka Ester,Zupancic-Salek Silva^ORCID

Publisher

Informa UK Limited

Subject

Health Policy,Pharmacology, Toxicology and Pharmaceutics (miscellaneous),Social Sciences (miscellaneous),Medicine (miscellaneous)

Reference38 articles.

1. European principles of haemophilia care

2. WFH Guidelines for the Management of Hemophilia, 3rd edition

3. Evolution of Haemophilia Care in Europe: 10 years of the principles of care

4. European Association of Hemophilia and Allied Disorders (EAHAD). Certification Centres; 2020. Available from: https://www.euhass.org/aspxpages/certcentres.aspx. Accessed October 26, 2020.

5. “What more can we ask for?”: an ethnographic study of challenges and possibilities for people living with haemophilia

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1. Normalisation of Haemostasis in Haemophilia A;EMJ Hematology;2024-07-25

2. Patient Perspective on Disease Burden and Gene Therapy for Hemophilia A and B: The “Haemvolution for Patients” Italian Survey;Seminars in Thrombosis and Hemostasis;2024-06-18

3. The psychosocial impact of haemophilia from patients’ and caregivers’ point of view: The results of an Italian survey;Haemophilia;2023-12-26

4. Real-World Experience of People with Hemophilia A Receiving Turoctocog Alfa Pegol (N8-GP): Results from a Patient Experience Survey;Patient Preference and Adherence;2023-11

5. Depression and anxiety among hemophilia patients enrolled in clinical trials: a multi-center cohort study;Annals of Hematology;2023-05-22