Search Results - Debbie Hicks

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  1. 1
    Optimising the Benefits of SGLT2 Inhibitors for Type 1 Diabetes

    Optimising the Benefits of SGLT2 Inhibitors for Type 1 Diabetes by Marc Evans, Debbie Hicks, Dipesh Patel, Vinod Patel, Phil McEwan, Umesh Dashora

    Published 2019
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  2. 2
    The clinical significance of sub-total surgical resection in childhood medulloblastoma: a multi-cohort analysis of 1100 patients

    The clinical significance of sub-total surgical resection in childhood medulloblastoma: a multi-cohort analysis of 1100 patients by Claire Keeling, Simon Davies, Jack Goddard, Vijay Ramaswamy, Ed C. Schwalbe, Simon Bailey, Debbie Hicks, Steven C. Clifford

    Published 2024
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  3. 3
    SGLT2 Inhibitors in Type 2 Diabetes Management: Key Evidence and Implications for Clinical Practice

    SGLT2 Inhibitors in Type 2 Diabetes Management: Key Evidence and Implications for Clinical Practice by John Wilding, Kevin Fernando, Nicola Milne, Marc Evans, Amar Ali, Steve Baín, Debbie Hicks, June James, Philip Newland‐Jones, Dipesh Patel, Adie Viljoen

    Published 2018
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  4. 4
    SGLT2 Inhibitors: Cardiovascular Benefits Beyond HbA1c—Translating Evidence into Practice

    SGLT2 Inhibitors: Cardiovascular Benefits Beyond HbA1c—Translating Evidence into Practice by Amar Ali, Steve Baín, Debbie Hicks, Phillip Newland Jones, Dipesh Patel, Marc Evans, Kevin Fernando, June James, Nicola Milne, Adie Viljoen, John Wilding

    Published 2019
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  5. 5
    Results and analysis of the 2008–2009 Insulin Injection Technique Questionnaire survey

    Results and analysis of the 2008–2009 Insulin Injection Technique Questionnaire survey by Carina DE CONINCK, Anders Frid, R Gaspar, Debbie Hicks, Lawrence J. Hirsch, Gillian Kreugel, J. Liersch, C. Letondeur, J.-P. Sauvanet, N Tubiana, Kenneth Strauss

    Published 2010
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  6. 6
    Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial

    Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial by Tobias Goschzik, Ed C. Schwalbe, Debbie Hicks, Amanda Smith, Anja zur Muehlen, Dominique Figarella‐Branger, François Doz, Stefan Rutkowski, Birgitta Lannering, Torsten Pietsch, Steven C. Clifford

    Published 2018
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  7. 7
    Risk Prediction of the Diabetes Missing Million: Identifying Individuals at High Risk of Diabetes and Related Complications

    Risk Prediction of the Diabetes Missing Million: Identifying Individuals at High Risk of Diabetes and Related Complications by Marc Evans, Angharad R. Morgan, Dipesh Patel, Ketan Dhatariya, Sharlene A. Greenwood, Philip Newland‐Jones, Debbie Hicks, Zaheer Yousef, Jim Moore, Bethany Kelly, Sarah Davies, Umesh Dashora

    Published 2020
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  8. 8
    New Insulin Delivery Recommendations

    New Insulin Delivery Recommendations by Anders Frid, Gillian Kreugel, G. Grassi, Serge Halimi, Debbie Hicks, Laurence Hirsch, Mike Smith, Regine Wellhoener, Bruce W. Bode, Irl B. Hirsch, Sanjay Kalra, Linong Ji, Kenneth Strauss

    Published 2016
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  9. 9
    Biomarker-driven stratification of disease-risk in non-metastatic medulloblastoma: Results from the multi-center HIT-SIOP-PNET4 clinical trial

    Biomarker-driven stratification of disease-risk in non-metastatic medulloblastoma: Results from the multi-center HIT-SIOP-PNET4 clinical trial by Steven C. Clifford, Birgitta Lannering, Ed C. Schwalbe, Debbie Hicks, Kieran Toole, Sarah Leigh Nicholson, Tobias Goschzik, Anja zur Mühlen, Dominique Figarella‐Branger, François Doz, Stefan Rutkowski, Göran Gustafsson, Torsten Pietsch

    Published 2015
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  10. 10
    Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy

    Mutations in the collagen XII gene define a new form of extracellular matrix-related myopathy by Debbie Hicks, Golara Torabi Farsani, S.H. Laval, James J. Collins, Anna Sárközy, E. Martoni, Aysha Haleem Shah, Yaqun Zou, Manuel Koch, Carsten G. Bönnemann, M. Roberts, Hanns Lochmüller, Kate Bushby, Volker Straub

    Published 2013
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  11. 11
    Time, pattern, and outcome of medulloblastoma relapse and their association with tumour biology at diagnosis and therapy: a multicentre cohort study

    Time, pattern, and outcome of medulloblastoma relapse and their association with tumour biology at diagnosis and therapy: a multicentre cohort study by Rebecca M. Hill, Stacey Richardson, Ed C. Schwalbe, Debbie Hicks, Janet C. Lindsey, Stephen Crosier, Gholamreza Rafiee, Yura Grabovska, Stephen B. Wharton, Thomas S. Jacques, Antony Michalski, Abhijit Joshi, Barry Pizer, Daniel Williamson, Simon Bailey, Steven C. Clifford

    Published 2020
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  12. 12
    Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study

    Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study by Ed C. Schwalbe, Janet C. Lindsey, Sirintra Nakjang, Stephen Crosier, Amanda Smith, Debbie Hicks, Gholamreza Rafiee, Rebecca M. Hill, Alice Iliasova, T. J. Stone, Barry Pizer, Antony Michalski, Abhijit Joshi, Stephen B. Wharton, Thomas S. Jacques, Simon Bailey, Daniel Williamson, Steven C. Clifford

    Published 2017
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  13. 13
    Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy

    Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy by Elizabeth Harris, Ana Töpf, Rita Barresi, Judith A. Hudson, Helen Powell, James O. Tellez, Debbie Hicks, Anna Porter, Marta Bértoli, Teresinha Evangelista, Chiara Marini-Betollo, Ólafur Þ. Magnússon, Monkol Lek, Daniel G. MacArthur, Kate Bushby, Hanns Lochmüller, Volker Straub

    Published 2017
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  14. 14
    Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice

    Recessive and dominant mutations in COL12A1 cause a novel EDS/myopathy overlap syndrome in humans and mice by Yaqun Zou, Daniela Zwolanek, Yayoi Izu, Shreya Gandhy, Gudrun Schreiber, Knut Brockmann, Marcella Devoto, Zuozhen Tian, Ying Hu, Guido Veit, Markus Meier, Jörg Stetefeld, Debbie Hicks, Volker Straub, Nicol C. Voermans, David E. Birk, Elisabeth R. Barton, Manuel Koch, Carsten G. Bönnemann

    Published 2013
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  15. 15
    Medulloblastoma group 3 and 4 tumors comprise a clinically and biologically significant expression continuum reflecting human cerebellar development

    Medulloblastoma group 3 and 4 tumors comprise a clinically and biologically significant expression continuum reflecting human cerebellar development by Daniel Williamson, Ed C. Schwalbe, Debbie Hicks, Kimberly A. Aldinger, Janet C. Lindsey, Stephen Crosier, Stacey Richardson, Jack Goddard, Rebecca M. Hill, Jemma Castle, Yura Grabovska, James Hacking, Barry Pizer, Stephen B. Wharton, Thomas S. Jacques, Abhijit Joshi, Simon Bailey, Steven C. Clifford

    Published 2022
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  16. 16
    A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy

    A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy by Debbie Hicks, Anna Sárközy, Nuria Muelas, Katrin Koehler, Angela Huebner, Gavin Hudson, Patrick F. Chinnery, Rita Barresi, Michelle Eagle, Tuomo Polvikoski, Geoff Bailey, James Miller, Aleksandar Radunović, PJ Hughes, R.G. Roberts, Sabine Krause, Maggie C. Walter, S. Laval, Volker Straub, Hanns Lochmüller, Kate Bushby

    Published 2010
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  17. 17
    Congenital myasthenic syndromes due to mutations in<i>ALG2</i>and<i>ALG14</i>

    Congenital myasthenic syndromes due to mutations in<i>ALG2</i>and<i>ALG14</i> by Judith Cossins, Katsiaryna Belaya, Debbie Hicks, Mustafa A. Salih, Sarah Finlayson, Nicola Carboni, Weiwei Liu, Susan Maxwell, Katarzyna Marta Zoltowska, Golara Torabi Farsani, Steven H. Laval, M.Z. Seidhamed, Peter Donnelly, David Bentley, Simon J. McGowan, Juliane Müller, Jacqueline Palace, Hanns Lochmüller, David Beeson

    Published 2013
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  18. 18
    Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance

    Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance by Anne Katrin Lampe, Yaqun Zou, D. Sudano, Kirsty O’Brien, Debbie Hicks, Steven H. Laval, Richard Charlton, C. Jimenez‐Mallebrera, Ruoyu Zhang, Richard S. Finkel, G. Tennekoon, Gudrun Schreiber, Marjo S. van der Knaap, Harold Marks, Volker Straub, Kevin M. Flanigan, Mon‐Li Chu, Francesco Muntoni, Kate Bushby, Carsten G. Bönnemann

    Published 2008
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  19. 19
    Natural history of pulmonary function in collagen VI-related myopathies

    Natural history of pulmonary function in collagen VI-related myopathies by A. Reghan Foley, Susana Quijano‐Roy, James J. Collins, Volker Straub, Michelle McCallum, Nicolas Deconinck, Eugenio Mercuri, Marika Pane, Adele D’Amico, Enrico Bertini, Kathryn N. North, Monique M. Ryan, Pascale Richard, Valérie Allamand, Debbie Hicks, Shireen R. Lamandé, Ying Hu, Francesca Gualandi, Sungyoung Auh, Francesco Muntoni, Carsten G. Bönnemann

    Published 2013
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  20. 20
    Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity

    Pediatric pan-central nervous system tumor analysis of immune-cell infiltration identifies correlates of antitumor immunity by Yura Grabovska, Alan Mackay, Patricia O’Hare, Stephen Crosier, Martina Finetti, Ed C. Schwalbe, Jessica C. Pickles, Amy R. Fairchild, Aimee Avery, Julia Cockle, Rebecca M. Hill, Janet C. Lindsey, Debbie Hicks, Mark Kristiansen, Jane Chalker, John Anderson, Darren Hargrave, Thomas S. Jacques, Karin Straathof, Simon Bailey, Chris Jones, Steven C. Clifford, Daniel Williamson

    Published 2020
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