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Original Research

Evaluating the impact of peer support and connection on the quality of life of patients with familial chylomicronemia syndrome

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Pages 497-505 | Received 19 Jun 2018, Accepted 24 Jul 2018, Published online: 05 Aug 2018

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Rina S. Fox, John Devin Peipert, Montserrat Vera-Llonch, Glenn Phillips & David Cella. (2020) PROMIS® and Neuro-QoLTM measures are valid measures of health-related quality of life among patients with familial chylomicronemia syndrome. Expert Review of Cardiovascular Therapy 18:4, pages 231-238.
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Articles from other publishers (3)

Maria Cristina de Oliveira Izar, Raul Dias dos SantosFilhoFilho, Marcelo Heitor Vieira Assad, Antonio Carlos Palandri Chagas, Alceu de Oliveira ToledoJúniorJúnior, Ana Cláudia Cavalcante Nogueira, Ana Cristina Carneiro Fernandes Souto, Ana Maria Pitta Lottenberg, Ana Paula Marte Chacra, Carlos Eduardo dos Santos Ferreira, Charles Marques Lourenço, Cynthia Melissa Valerio, Dennys Esper Cintra, Francisco Antonio Helfenstein Fonseca, Gustavo Aguiar Campana, Henrique Tria Bianco, Josivan Gomes de Lima, Maria Helane Costa Gurgel Castelo, Marileia Scartezini, Miguel Antonio Moretti, Natasha Slhessarenko Fraife Barreto, Rayana Elias Maia, Renan Magalhães MontenegroJuniorJunior, Renato Jorge Alves, Roberta Marcondes Machado Figueiredo, Rodrigo Ambrosio Fock & Tânia Leme da Rocha Martinez. (2023) Posicionamento Brasileiro sobre Síndrome da Quilomicronemia Familiar – 2023. Arquivos Brasileiros de Cardiologia 120:4.
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Karen Kaiser, Rina S. Fox, Chelsea Perschon, Montserrat Vera-Llonch, Jordi Alonso, Laia Cubells & David Cella. (2022) Qualitative development of the PROMIS Profile v1.0-Familial Chylomicronemia Syndrome (FCS) 28. Quality of Life Research.
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C.K. Zigler, K. Ardalan, A. Hernandez, A.E. Caliendo, K.E. Magee, M.A. Terry, C.M. Mann & K.S. Torok. (2020) Exploring the impact of paediatric localized scleroderma on health‐related quality of life: focus groups with youth and caregivers. British Journal of Dermatology 183:4, pages 692-701.
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