Summary of Research: Caregiver Involvement in MS: Duty or Disruption?

por Kesselring, Jürg, Boyko, Alexey, Laroni, Alice, Bharadia, Trishna, van Galen, Pieter, Alexandri, Nektaria
Publicado 2023

Caregiver Involvement in MS: Duty or Disruption?

por Kesselring, Jürg, Boyko, Alexey, Laroni, Alice, Bharadia, Trishna, van Galen, Pieter, Alexandri, Nektaria
Publicado 2021

Patient-reported outcome measures in MS: Do development processes and patient involvement support valid quantification of clinically important variables?

por Bharadia, Trishna, Vandercappellen, Jo, Chitnis, Tanuja, Eelen, Piet, Bauer, Birgit, Brichetto, Giampaolo, Lloyd, Andrew, Schmidt, Hollie, King, Miriam, Fitzgerald, Jennifer, Hach, Thomas, Hobart, Jeremy
Publicado 2022

Disease Progression in Multiple Sclerosis: A Literature Review Exploring Patient Perspectives

por Celius, Elisabeth G, Thompson, Heidi, Pontaga, Maija, Langdon, Dawn, Laroni, Alice, Potra, Stanca, Bharadia, Trishna, Yeandle, David, Shanahan, Jane, van Galen, Pieter, Alexandri, Nektaria, Kesselring, Jürg
Publicado 2021

Tailoring STrAtegies for RelaTives for Black and South Asian dementia family carers in the United Kingdom: A mixed methods study

por Webster, Lucy, Amador, Sarah, Rapaport, Penny, Mukadam, Naaheed, Sommerlad, Andrew, James, Tiffeny, Javed, Sabrina, Roche, Moïse, Lord, Kathryn, Bharadia, Trishna, Rahman‐Amin, Malayka, Lang, Iain, Livingston, Gill
Publicado 2023