Torthaí cuardaigh - Atul Mehta

Beachtaigh na torthaí
  1. 1
    Glucose-6-phosphate dehydrogenase deficiency

    Glucose-6-phosphate dehydrogenase deficiency de réir Atul Mehta

    Foilsithe / Cruthaithe 1994
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  2. 2
    Gaucher disease: haematological presentations and complications

    Gaucher disease: haematological presentations and complications de réir Alison Thomas, Atul Mehta, Derralynn Hughes

    Foilsithe / Cruthaithe 2014
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  3. 3
    How we manage Gaucher Disease in the era of choices

    How we manage Gaucher Disease in the era of choices de réir Shoshana Revel‐Vilk, Jeff Szer, Atul Mehta, Ari Zimran

    Foilsithe / Cruthaithe 2018
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  4. 4
    Mycophenolate mofetil for the treatment of refractory auto‐immune haemolytic anaemia and auto‐immune thrombocytopenia purpura

    Mycophenolate mofetil for the treatment of refractory auto‐immune haemolytic anaemia and auto‐immune thrombocytopenia purpura de réir Jo Howard, A. V. Hoffbrand, H. G. Prentice, Atul Mehta

    Foilsithe / Cruthaithe 2002
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  5. 5
    A clinical and family history study of Parkinson's disease in heterozygous<i>glucocerebrosidase</i>mutation carriers

    A clinical and family history study of Parkinson's disease in heterozygous<i>glucocerebrosidase</i>mutation carriers de réir Alisdair McNeill, Raquel Durán, Derralynn Hughes, Atul Mehta, Anthony H.V. Schapira

    Foilsithe / Cruthaithe 2012
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  6. 6
    Thrombopoietin concentrations are low in patients with cirrhosis and thrombocytopenia and are restored after orthotopic liver transplantation

    Thrombopoietin concentrations are low in patients with cirrhosis and thrombocytopenia and are restored after orthotopic liver transplantation de réir John Goulis, T N Chau, S Jordan, Atul Mehta, A. Watkinson, Keith Rolles, Andrew K. Burroughs

    Foilsithe / Cruthaithe 1999
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  7. 7
    Evolution of Prodromal Clinical Markers of Parkinson Disease in a<i>GBA</i>Mutation–Positive Cohort

    Evolution of Prodromal Clinical Markers of Parkinson Disease in a<i>GBA</i>Mutation–Positive Cohort de réir Michelle Beavan, Alisdair McNeill, Christos Proukakis, Derralynn Hughes, Atul Mehta, Anthony H.V. Schapira

    Foilsithe / Cruthaithe 2014
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  8. 8
    Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome survey

    Cardiac manifestations of Anderson-Fabry disease: results from the international Fabry outcome survey de réir Aleš Linhart, Christoph Kampmann, José Luis Zamorano, Gere Sunder‐Plassmann, Michael Beck, Atul Mehta, Perry Elliott

    Foilsithe / Cruthaithe 2007
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  9. 9
    Clinical prodromes of neurodegeneration in Anderson-Fabry disease

    Clinical prodromes of neurodegeneration in Anderson-Fabry disease de réir Matthias Löhle, Derralynn Hughes, Alan Milligan, Linda Richfield, Heinz Reichmann, Atul Mehta, Anthony H.V. Schapira

    Foilsithe / Cruthaithe 2015
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  10. 10
    The Binary Endocardial Appearance Is a Poor Discriminator of Anderson-Fabry Disease From Familial Hypertrophic Cardiomyopathy

    The Binary Endocardial Appearance Is a Poor Discriminator of Anderson-Fabry Disease From Familial Hypertrophic Cardiomyopathy de réir Stavros P. Kounas, Camelia Demetrescu, Antonios Pantazis, Andre Keren, Philip Lee, Derralynn Hughes, Atul Mehta, Perry Elliott

    Foilsithe / Cruthaithe 2008
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  11. 11
    Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome Survey

    Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome Survey de réir Atul Mehta, Joe T.R. Clarke, Roberto Giugliani, Perry Elliott, Aleš Linhart, Michael Beck, Gere Sunder‐Plassmann

    Foilsithe / Cruthaithe 2009
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  12. 12
    Stages of T-cell receptor protein expression in T-cell acute lymphoblastic leukemia

    Stages of T-cell receptor protein expression in T-cell acute lymphoblastic leukemia de réir Dario Campana, JJ van Dongen, Atul Mehta, Elaine Coustan‐Smith, IL Wolvers-Tettero, K. Ganeshaguru, George Janossy

    Foilsithe / Cruthaithe 1991
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  13. 13
    Phenotype and biochemical heterogeneity in late onset Fabry disease defined by N215S mutation

    Phenotype and biochemical heterogeneity in late onset Fabry disease defined by N215S mutation de réir Lucia Lavalle, A. Thomas, Brendan Beaton, H. Ebrahim, Malcolm Reed, Uma Ramaswami, Perry Elliott, Atul Mehta, Derralynn Hughes

    Foilsithe / Cruthaithe 2018
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  14. 14
    A charitable access program for patients with lysosomal storage disorders in underserved communities worldwide

    A charitable access program for patients with lysosomal storage disorders in underserved communities worldwide de réir Atul Mehta, Uma Ramaswami, Joseph Muenzer, Roberto Giugliani, Kurt Ullrich, Tanya Collin-Histed, Zoya Panahloo, Hartmann Wellhoefer, Joel Frader

    Foilsithe / Cruthaithe 2021
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  15. 15
    Fabry disease: a review of current management strategies

    Fabry disease: a review of current management strategies de réir Atul Mehta, Michael Beck, F. Eyskens, Claudio Feliciani, Ilkka Kantola, Uma Ramaswami, A. Rolfs, A. Rivera, S. Waldek, Dominique P. Germain

    Foilsithe / Cruthaithe 2010
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  16. 16
    Gaucher Cells Demonstrate a Distinct Macrophage Phenotype and Resemble Alternatively Activated Macrophages

    Gaucher Cells Demonstrate a Distinct Macrophage Phenotype and Resemble Alternatively Activated Macrophages de réir Leonie A. Boven, Marjan van Meurs, Rolf G. Boot, Atul Mehta, Louis Boon, Johannes M. F. G. Aerts, Jon D. Laman

    Foilsithe / Cruthaithe 2004
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  17. 17
    Cardiac Fabry Disease With Late Gadolinium Enhancement Is a Chronic Inflammatory Cardiomyopathy

    Cardiac Fabry Disease With Late Gadolinium Enhancement Is a Chronic Inflammatory Cardiomyopathy de réir Sabrina Nordin, Rebecca Kozor, Heerajnarain Bulluck, Silvia Castelletti, Stefania Rosmini, Amna Abdel‐Gadir, Shanat Baig, Atul Mehta, Derralynn Hughes, James Moon

    Foilsithe / Cruthaithe 2016
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  18. 18
    Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease

    Assessment of plasma lyso-Gb3 for clinical monitoring of treatment response in migalastat-treated patients with Fabry disease de réir Daniel G. Bichet, Johannes M. F. G. Aerts, Christiane Auray‐Blais, Hiroki Maruyama, Atul Mehta, Nina Skuban, Eva Krusinska, Raphael Schiffmann

    Foilsithe / Cruthaithe 2020
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  19. 19
    Gaucher Cells Demonstrate a Distinct Macrophage Phenotype and Resemble Alternatively Activated Macrophages

    Gaucher Cells Demonstrate a Distinct Macrophage Phenotype and Resemble Alternatively Activated Macrophages de réir Leonie A. Boven, Marjan van Meurs, Rolf G. Boot, Atul Mehta, Louis Boon, Johannes M. F. G. Aerts, Jon D. Laman

    Foilsithe / Cruthaithe 2004
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  20. 20
    Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis

    Long-term effectiveness of agalsidase alfa enzyme replacement in Fabry disease: A Fabry Outcome Survey analysis de réir Michael Beck, Derralynn Hughes, Christoph Kampmann, Sylvain Larroque, Atul Mehta, Guillem Pintos‐Morell, Uma Ramaswami, Michael L. West, Anna Wijatyk, Roberto Giugliani

    Foilsithe / Cruthaithe 2015
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