Ngā hua rapu - Kerry Leeson‐Beevers

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  1. 1
    ‘I Have my Beliefs, but Then I Have my Reality’: Reflections of Black and South Asian Parents Living in England on Screening and Genetic Diagnosis in Pregnancy

    ‘I Have my Beliefs, but Then I Have my Reality’: Reflections of Black and South Asian Parents Living in England on Screening and Genetic Diagnosis in Pregnancy mā Michelle Peter, Rashida Baptiste, Rachael Buabeng, Lily Islam, Jane Fisher, Kerry Leeson‐Beevers, Melissa Hill, Lyn S. Chitty

    I whakaputaina 2025
    Whiwhi kuputuhi katoa
    Artigo
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  2. 2
    How are patients with rare diseases and their carers in the UK impacted by the way care is coordinated? An exploratory qualitative interview study

    How are patients with rare diseases and their carers in the UK impacted by the way care is coordinated? An exploratory qualitative interview study mā Amy Simpson, Lara Bloom, Naomi Fulop, Emma Hudson, Kerry Leeson‐Beevers, Stephen Morris, Angus Ramsay, Alastair Sutcliffe, Holly Walton, Amy Hunter

    I whakaputaina 2021
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  3. 3
    Development of models of care coordination for rare conditions: a qualitative study

    Development of models of care coordination for rare conditions: a qualitative study mā Holly Walton, Amy Simpson, Angus Ramsay, Amy Hunter, Jennifer Jones, Pei Li Ng, Kerry Leeson‐Beevers, Lara Bloom, Joe Kai, Maria Kokocinska, Alastair Sutcliffe, Stephen Morris, Naomi Fulop

    I whakaputaina 2022
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  4. 4
    The patient’s view on rare disease trial design – a qualitative study

    The patient’s view on rare disease trial design – a qualitative study mā Charlotte M. W. Gaasterland, M. C. Jansen – van der Weide, M. J. du Prie – Olthof, Mieke Donk, Marleen M. Kaatee, Radosław Kaczmarek, Christine Lavery, Kerry Leeson‐Beevers, Nina O’Neill, Oliver Timmis, V. van Nederveen, E. Vroom, J. H. van der Lee

    I whakaputaina 2019
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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  5. 5
    Consensus clinical management guidelines for Alström syndrome

    Consensus clinical management guidelines for Alström syndrome mā Natascia Tahani, Pietro Maffei, Hélène Dollfus, Richard Paisey, Diana Valverde, Gabriella Milan, Joan C. Han, Francesca Favaretto, Shyam Madathil, Charlotte Dawson, Matthew J. Armstrong, Adrian Warfield, Selma Düzenli, Clair A. Francomano, Meral Gunay‐Aygun, Francesca Dassie, Vincent Marion, M. Valenti, Kerry Leeson-Beevers, A Chivers, Richard P. Steeds, Timothy Barrett, Tarekegn Geberhiwot

    I whakaputaina 2020
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Revisão
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  6. 6
    ‘Something that helped the whole picture’: Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service

    ‘Something that helped the whole picture’: Experiences of parents offered rapid prenatal exome sequencing in routine clinical care in the English National Health Service mā Hannah McInnes‐Dean, Rhiannon Mellis, Morgan Daniel, Holly Walton, Emma L. Baple, Marta Bértoli, Jane Fisher, Katarzyna Gajewska‐Knapik, Muriel Holder‐Espinasse, Caroline Lafarge, Kerry Leeson‐Beevers, Alec McEwan, Pranav Pandya, Michael Parker, Sophie Peet, Lauren Roberts, Srividhya Sankaran, Audrey Smith, Dagmar Tapon, Wing Han Wu, Sarah L. Wynn, Lyn S. Chitty, Melissa Hill, Michelle Peter

    I whakaputaina 2024
    Whiwhi kuputuhi katoa Whiwhi kuputuhi katoa
    Artigo
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