Torthaí cuardaigh - 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 de réir Michelle Peter, Rashida Baptiste, Rachael Buabeng, Lily Islam, Jane Fisher, Kerry Leeson‐Beevers, Melissa Hill, Lyn S. Chitty

    Foilsithe / Cruthaithe 2025
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    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 de réir Amy Simpson, Lara Bloom, Naomi Fulop, Emma Hudson, Kerry Leeson‐Beevers, Stephen Morris, Angus Ramsay, Alastair Sutcliffe, Holly Walton, Amy Hunter

    Foilsithe / Cruthaithe 2021
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    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 de réir 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

    Foilsithe / Cruthaithe 2022
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    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 de réir 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

    Foilsithe / Cruthaithe 2019
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    Artigo
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  5. 5
    Consensus clinical management guidelines for Alström syndrome

    Consensus clinical management guidelines for Alström syndrome de réir 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

    Foilsithe / Cruthaithe 2020
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    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 de réir 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

    Foilsithe / Cruthaithe 2024
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    Artigo
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