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1

Glucose-6-phosphate dehydrogenase deficiency حسب Atul Mehta

منشور في 1994

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Revisão

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2

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

منشور في 2014

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Revisão

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3

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

منشور في 2018

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Revisão

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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 حسب Jo Howard, A. V. Hoffbrand, H. G. Prentice, Atul Mehta

منشور في 2002

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Artigo

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5

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

منشور في 2012

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Carta

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6

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

منشور في 1999

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Artigo

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7

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

منشور في 2014

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Artigo

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8

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

منشور في 2007

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Artigo

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9

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

منشور في 2015

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Artigo

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10

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

منشور في 2008

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Artigo

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11

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

منشور في 2009

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Artigo

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12

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

منشور في 1991

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Artigo

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13

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

منشور في 2018

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Artigo

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14

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

منشور في 2021

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Artigo

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محفوظ في:
15

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

منشور في 2010

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Revisão

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16

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

منشور في 2004

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Artigo

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17

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

منشور في 2016

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Carta

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18

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

منشور في 2020

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Artigo

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19

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

منشور في 2004

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Artigo

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20

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

منشور في 2015

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Artigo

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محفوظ في:

نتائج البحث - Atul Mehta

Glucose-6-phosphate dehydrogenase deficiency حسب Atul Mehta

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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