Torthaí cuardaigh - Catherine Peters

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  1. 1
    DIAGNOSIS OF ENDOCRINE DISEASE: Congenital hypothyroidism: update and perspectives

    DIAGNOSIS OF ENDOCRINE DISEASE: Congenital hypothyroidism: update and perspectives de réir Catherine Peters, A.S. Paul van Trotsenburg, Nadia Schoenmakers

    Foilsithe / Cruthaithe 2018
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  2. 2
    Screening for Congenital Hypothyroidism: Comparison of Borderline Screening Cut-Off Points and the Effect on the Number of Children Treated with Levothyroxine

    Screening for Congenital Hypothyroidism: Comparison of Borderline Screening Cut-Off Points and the Effect on the Number of Children Treated with Levothyroxine de réir Shirley Langham, Peter C. Hindmarsh, Steven Krywawych, Catherine Peters

    Foilsithe / Cruthaithe 2013
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  3. 3
    Cardiovascular risk factors in children and adolescents with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency

    Cardiovascular risk factors in children and adolescents with congenital adrenal hyperplasia due to 21‐hydroxylase deficiency de réir Anbezhil Subbarayan, Mehul Dattani, Catherine Peters, Peter C. Hindmarsh

    Foilsithe / Cruthaithe 2013
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  4. 4
    The SARS‐CoV‐2 pandemic is associated with increased severity of presentation of childhood onset type 1 diabetes mellitus: A multi‐centre study of the first COVID‐19 wave

    The SARS‐CoV‐2 pandemic is associated with increased severity of presentation of childhood onset type 1 diabetes mellitus: A multi‐centre study of the first COVID‐19 wave de réir Sinead McGlacken‐Byrne, Samantha Drew, Kelly Turner, Catherine Peters, Rakesh Amin

    Foilsithe / Cruthaithe 2021
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  5. 5
    Management of Cushing syndrome in children and adolescents: experience of a single tertiary centre

    Management of Cushing syndrome in children and adolescents: experience of a single tertiary centre de réir María Güemes, Philip Murray, Caroline Brain, Helen Spoudeas, Catherine Peters, Peter C. Hindmarsh, Mehul Dattani

    Foilsithe / Cruthaithe 2016
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  6. 6
    Defining the Newborn Blood Spot Screening Reference Interval for TSH: Impact of Ethnicity

    Defining the Newborn Blood Spot Screening Reference Interval for TSH: Impact of Ethnicity de réir Catherine Peters, Ivan Brooke, Simon Heales, Adeboye Ifederu, Shirley Langham, Peter C. Hindmarsh, Tim Cole

    Foilsithe / Cruthaithe 2016
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  7. 7
    <i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom

    <i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom de réir Catherine Peters, Adeline K. Nicholas, Erik Schoenmakers, Greta Lyons, Shirley Langham, Eva Serra, Neil J. Sebire, Marina Muzza, Laura Fugazzola, Nadia Schoenmakers

    Foilsithe / Cruthaithe 2019
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  8. 8
    Impact of Electronic Health Record Use on Cognitive Load and Burnout Among Clinicians: Narrative Review

    Impact of Electronic Health Record Use on Cognitive Load and Burnout Among Clinicians: Narrative Review de réir Elham Asgari, Japsimar Kaur, Gani Nuredini, Jasmine Balloch, Andrew M. Taylor, Neil J. Sebire, Robert Robinson, Catherine Peters, Shankar Sridharan, Dominic Pimenta

    Foilsithe / Cruthaithe 2024
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  9. 9
    Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD)

    Thioredoxin Reductase 2 (TXNRD2) Mutation Associated With Familial Glucocorticoid Deficiency (FGD) de réir Rathi Prasad, Li Chan, Claire Hughes, Juan Pablo Kaski, Julia Kowalczyk, Martin O. Savage, Catherine Peters, Nisha Nathwani, Adrian Clark, Helen L. Storr, Lou Metherell

    Foilsithe / Cruthaithe 2014
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  10. 10
    Assisted reproductive therapies and imprinting disorders—a preliminary British survey

    Assisted reproductive therapies and imprinting disorders—a preliminary British survey de réir Alastair Sutcliffe, Catherine Peters, Sarah Bowdin, I. Karen Temple, William Reardon, Lisa M Wilson, Jill Clayton‐Smith, L A Brueton, Wendy Bannister, Eamonn R. Maher

    Foilsithe / Cruthaithe 2005
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  11. 11
    Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology

    Congenital Hypothyroidism: A 2020–2021 Consensus Guidelines Update—An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and th... de réir A.S. Paul van Trotsenburg, Athanasia Stoupa, Juliane Léger, Tilman Rohrer, Catherine Peters, Laura Fugazzola, Alessandra Cassio, Claudine Heinrichs, Véronique Beauloye, Joachim Pohlenz, Patrice Rodien, R. Coutant, Gabor Szinnai, Philip Murray, Beate Bartès, Dominique Luton, Mariacarolina Salerno, Luisa De Sanctis, Mariacristina Vigone, Heiko Krude, Luca Persani, Michel Polak

    Foilsithe / Cruthaithe 2020
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  12. 12
    Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

    Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability de réir Anne Raimondo, Ali Chakera, Soren K. Thomsen, Kevin Colclough, Amy Barrett, Elisa De Franco, Alisson Chatelas, Hüseyin Demirbilek, Teoman Akçay, Hussein Alawneh, Sarah E. Flanagan, Martijn van de Bunt, Andrew T. Hattersley, Anna L. Gloyn, Sian Ellard, Mohammad A. Abduljabbar, Mahmoud Alzyoud, Syed Aman, Louise Bath, Parijat De, Neeta Deshpande, Erdem Durmaz, Frank Eickmeier, Nancy Samir Elbarbary, Marc Fillion, Sujatha Jagadeesh, Melanie Kershaw, Waqas Khan, Wojciech Młynarski, Kathryn Noyes, Catherine Peters, Nick Shaw, Irina Tiron, Doğa Türkkahraman, Lesley Turner, Khadiga Eltonbary, Bilgin Yüksel

    Foilsithe / Cruthaithe 2014
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  13. 13
    Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ

    Comprehensive Screening of Eight Known Causative Genes in Congenital Hypothyroidism With Gland-in-Situ de réir Adeline K. Nicholas, Eva Serra, Hakan Cangül, Saif Al-Yaarubi, Irfan Ullah, Erik Schoenmakers, Asma Deeb, Abdelhadi Habeb, Mohammad S. Al-Maghamsi, Catherine Peters, Nisha Nathwani, Zehra Aycan, Halil Sağlam, Ece Böber, Mehul Dattani, Savitha Shenoy, Philip Murray, Amir Babiker, Ruben H. Willemsen, Ajay Thankamony, Greta Lyons, Rachael Irwin, Raja Padidela, Kavitha Tharian, Justin H. Davies, Vijith Puthi, Soo‐Mi Park, Ahmed F. Massoud, John W Gregory, Assunta Albanese, Evelien Pease-Gevers, Howard Martin, Kim Brügger, Eamonn R. Maher, Krishna Chatterjee, Carl A. Anderson, Nadia Schoenmakers

    Foilsithe / Cruthaithe 2016
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