Bilaketaren emaitzak - Philip Murray

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  1. 1
    Endocrine Control of Growth

    Endocrine Control of Growth nork Philip Murray, Peter Clayton

    Argitaratua 2013
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  2. 2
    60 YEARS OF NEUROENDOCRINOLOGY: The hypothalamo-GH axis: the past 60 years

    60 YEARS OF NEUROENDOCRINOLOGY: The hypothalamo-GH axis: the past 60 years nork Philip Murray, Claire Higham, Peter Clayton

    Argitaratua 2015
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  3. 3
    Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence

    Controversies in the diagnosis and management of growth hormone deficiency in childhood and adolescence nork Philip Murray, Mehul Dattani, Peter Clayton

    Argitaratua 2015
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  4. 4
    A genetic approach to evaluation of short stature of undetermined cause

    A genetic approach to evaluation of short stature of undetermined cause nork Philip Murray, Peter Clayton, Steven D. Chernausek

    Argitaratua 2018
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  5. 5
    Vasoactive Intestinal Peptide and the Watery Diarrhea Syndrome

    Vasoactive Intestinal Peptide and the Watery Diarrhea Syndrome nork Amin M. Ebeid, Philip Murray, Josef E. Fischer

    Argitaratua 1978
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  6. 6
    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 nork María Güemes, Philip Murray, Caroline Brain, Helen Spoudeas, Catherine Peters, Peter C. Hindmarsh, Mehul Dattani

    Argitaratua 2016
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  7. 7
    Exploring the spectrum of 3‐M syndrome, a primordial short stature disorder of disrupted ubiquitination

    Exploring the spectrum of 3‐M syndrome, a primordial short stature disorder of disrupted ubiquitination nork Peter Clayton, Dan Hanson, Lucia Magee, Philip Murray, Emma Saunders, Sayeda N. Abu‐Amero, Gudrun E. Moore, Graeme Black

    Argitaratua 2012
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  8. 8
    The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1

    The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1 nork Dan Hanson, Philip Murray, Amit Sud, Samia A. Temtamy, Mona Aglan, Andrea Superti‐Furga, Sue Holder, Jill Urquhart, Emma Hilton, Forbes D.C. Manson, Peter Scambler, Graeme Black, Peter Clayton

    Argitaratua 2009
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  9. 9
    Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth

    Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth nork Dan Hanson, Philip Murray, James O’Sullivan, Jill Urquhart, Sarah B. Daly, Sanjeev S. Bhaskar, Leslie G. Biesecker, Mars Skae, Claire E. L. Smith, Trevor Cole, Jeremy Kirk, Kate Chandler, Helen Kingston, Dian Donnai, Peter Clayton, Graeme Black

    Argitaratua 2011
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  10. 10
    Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling

    Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling nork Dan Hanson, Philip Murray, Tessa Coulson, Amit Sud, Ajibola Omokanye, Emily Stratta, Faezeh Sakhinia, C Bonshek, Laura C. Wilson, Emma Wakeling, Samia A. Temtamy, Mona Aglan, Elisabeth Rosser, Sahar Mansour, Atilano Carcavilla, Sheela Nampoothiri, Waqas Khan, Indraneel Banerjee, Kate Chandler, Graeme Black, Peter Clayton

    Argitaratua 2012
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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... nork 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

    Argitaratua 2020
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  12. 12
    Diagnosis and management of Silver–Russell syndrome: first international consensus statement

    Diagnosis and management of Silver–Russell syndrome: first international consensus statement nork Emma Wakeling, Frédéric Brioude, Oluwakemi Lokulo‐Sodipe, Susan O’Çonnell, Jennifer Ben Salem, Jet Bliek, Ana Pinheiro Machado Canton, Krystyńa Chrzańowska, Justin H. Davies, Renuka Dias, B. Dubern, Miriam Elbracht, Éloïse Giabicani, Adda Grimberg, Karen Grønskov, Anita C. S. Hokken‐Koelega, Alexander A.L. Jorge, Masayo Kagami, Agnès Linglart, Mohamad Maghnie, Klaus Mohnike, David Monk, Gudrun E. Moore, Philip Murray, Tsutomu Ogata, Isabelle Petit, Silvia Russo, Edith Said, Meropi Toumba, Zeynep Tümer, Gerhard Binder, Thomas Eggermann, Madeleine D. Harbison, I. Karen Temple, Deborah Mackay, Irène Netchine

    Argitaratua 2016
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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 nork 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

    Argitaratua 2016
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  14. 14
    Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients

    Recommendations for Diagnosis and Treatment of Pseudohypoparathyroidism and Related Disorders: An Updated Practical Tool for Physicians and Patients nork Giovanna Mantovani, Murat Bastepe, David Monk, Luisa De Sanctis, Susanne Thiele, S. Faisal Ahmed, Roberto Bufo, Timothée Choplin, Gianpaolo De Filippo, Guillemette Devernois, Thomas Eggermann, Francesca Marta Elli, Aurora García Ramirez, Emily L. Germain‐Lee, Lionel Groussin, Neveen A. T. Hamdy, Patrick Hanna, Olaf Hiort, Harald Jüppner, Peter Kamenický, Nina Knight, Elvire Le Norcy, Beatriz Lecumberri, Michael A. Levine, Outi Mäkitie, Regina Matsunaga Martin, Gabriel Ángel Martos‐Moreno, Manasori Minagawa, Philip Murray, Arrate Pereda, Robert J. Pignolo, Lars Rejnmark, Rebeca Rodado, Anya Rothenbühler, Vrinda Saraff, Ashley H. Shoemaker, Eileen M. Shore, Caroline Silve, Serap Turan, Philip R. Woods, M. Carola Zillikens, Guiomar Pérez de Nanclares, Agnès Linglart

    Argitaratua 2020
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  15. 15
    Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement

    Diagnosis and management of pseudohypoparathyroidism and related disorders: first international Consensus Statement nork Giovanna Mantovani, Murat Bastepe, David Monk, Luisa De Sanctis, Susanne Thiele, Alessia Usardi, S. Faisal Ahmed, Roberto Bufo, Timothée Choplin, Gianpaolo De Filippo, Guillemette Devernois, Thomas Eggermann, Francesca Marta Elli, Kathleen Freson, Aurora García Ramirez, Emily L. Germain‐Lee, Lionel Groussin, Neveen A. T. Hamdy, Patrick Hanna, Olaf Hiort, Harald Jüppner, Peter Kamenický, Nina Knight, Marie-Laure Kottler, Elvire Le Norcy, Beatriz Lecumberri, Michael A. Levine, Outi Mäkitie, Regina Matsunaga Martin, Gabriel Ángel Martos‐Moreno, Masanori Minagawa, Philip Murray, Arrate Pereda, Robert J. Pignolo, Lars Rejnmark, Rebecca Rodado, Anya Rothenbühler, Vrinda Saraff, Ashley H. Shoemaker, Eileen M. Shore, Caroline Silve, Serap Turan, Philip R. Woods, M. Carola Zillikens, Guiomar Pérez de Nanclares, Agnès Linglart

    Argitaratua 2018
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