The psychosocial impact of haemophilia from patients’ and caregivers’ point of view: The results of an Italian survey
Arianna Fornari(Fondazione IRCCS Istituto Neurologico Carlo Besta), LG Mantovani(IRCCS Istituto Auxologico Italiano), Paolo Cozzolino(MultiMedica), Rita Facchetti(Laiko General Hospital of Athens), Nicola Ceresi(Haemophilia Foundation Australia), Paolo Angelo Cortesi(University of Milano-Bicocca), Chiara Biasoli(Ospedale “M. Bufalini” di Cesena), Anna Fragomeno(Haemophilia Foundation Australia), Francesco Cucuzza(Haemophilia Foundation Australia), Cristina Santoro(Sapienza University of Rome), Ippazio Cosimo Antonazzo(University of Bergen), Antonio Coppola(University of Cagliari), Daniele Preti(Haemophilia Foundation Australia), Antonietta Ferretti(Policlinico Umberto I), Cristina Cassone(Haemophilia Foundation Australia), Angiola Rocino(Azienda Ospedaliero-Universitaria Careggi)
Cited by 12
Related Papers
Global, regional, and national burden of stroke and its risk factors, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019
|The Lancet Neurology|2021|7.9k
Prognostic Value of Ambulatory and Home Blood Pressures Compared With Office Blood Pressure in the General Population
|Circulation|2005|1k
Long-Term Risk of Mortality Associated With Selective and Combined Elevation in Office, Home, and Ambulatory Blood Pressure
|Hypertension|2006|693
Global Burden of Multiple Myeloma
|JAMA Oncology|2018|631
Long-Term Prognostic Value of Blood Pressure Variability in the General Population
|Hypertension|2007|375