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Orphanet Journal of Rare Diseases
|
June 17, 2015
Quality of life in patients with Fabry disease: a systematic review of the literature
Maarten Arends, Carla E M Hollak, Marieke Biegstraaten
Molecular Genetics and Metabolism
|
December 15, 2015
Discontinuation of enzyme replacement therapy in Fabry disease in the Dutch cohort
Maarten Arends, Gabor E Linthorst, Carla E Hollak, et al.
British Journal of Haematology
|
April 19, 2013
Malignancies and monoclonal gammopathy in Gaucher disease; a systematic review of the literature
Maarten Arends, Laura van Dussen, Marieke Biegstraaten, et al.
Drug Discovery Today
|
February 19, 2018
Adaptive pathway development for Fabry disease: a clinical approach
Yvonne Schuller, Maarten Arends, Simon Körver, et al.
Journal of Inherited Metabolic Disease
|
October 18, 2017
Phenotype, disease severity and pain are major determinants of quality of life in Fabry disease: results from a large multicenter cohort study
Maarten Arends, Simon Körver, Derralynn A Hughes, et al.
Journal of the American Society of Nephrology : JASN
|
December 17, 2016
Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study
Maarten Arends, Christoph Wanner, Derralynn Hughes, et al.
Molecular Genetics and Metabolism
|
May 13, 2017
Favourable effect of early versus late start of enzyme replacement therapy on plasma globotriaosylsphingosine levels in men with classical Fabry disease
Maarten Arends, Frits A Wijburg, Christoph Wanner, et al.
Plos One
|
August 2, 2017
Retrospective study of long-term outcomes of enzyme replacement therapy in Fabry disease: Analysis of prognostic factors
Maarten Arends, Marieke Biegstraaten, Derralynn A Hughes, et al.
Journal of Medical Genetics
|
February 14, 2018
Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study
Maarten Arends, Marieke Biegstraaten, Christoph Wanner, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Orphanet Journal of Rare Diseases
|
June 17, 2015
Quality of life in patients with Fabry disease: a systematic review of the literature
Maarten Arends, Carla E M Hollak, Marieke Biegstraaten
Molecular Genetics and Metabolism
|
December 15, 2015
Discontinuation of enzyme replacement therapy in Fabry disease in the Dutch cohort
Maarten Arends, Gabor E Linthorst, Carla E Hollak, et al.
British Journal of Haematology
|
April 19, 2013
Malignancies and monoclonal gammopathy in Gaucher disease; a systematic review of the literature
Maarten Arends, Laura van Dussen, Marieke Biegstraaten, et al.
Drug Discovery Today
|
February 19, 2018
Adaptive pathway development for Fabry disease: a clinical approach
Yvonne Schuller, Maarten Arends, Simon Körver, et al.
Journal of Inherited Metabolic Disease
|
October 18, 2017
Phenotype, disease severity and pain are major determinants of quality of life in Fabry disease: results from a large multicenter cohort study
Maarten Arends, Simon Körver, Derralynn A Hughes, et al.
Journal of the American Society of Nephrology : JASN
|
December 17, 2016
Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study
Maarten Arends, Christoph Wanner, Derralynn Hughes, et al.
Molecular Genetics and Metabolism
|
May 13, 2017
Favourable effect of early versus late start of enzyme replacement therapy on plasma globotriaosylsphingosine levels in men with classical Fabry disease
Maarten Arends, Frits A Wijburg, Christoph Wanner, et al.
Plos One
|
August 2, 2017
Retrospective study of long-term outcomes of enzyme replacement therapy in Fabry disease: Analysis of prognostic factors
Maarten Arends, Marieke Biegstraaten, Derralynn A Hughes, et al.
Journal of Medical Genetics
|
February 14, 2018
Agalsidase alfa versus agalsidase beta for the treatment of Fabry disease: an international cohort study
Maarten Arends, Marieke Biegstraaten, Christoph Wanner, et al.
Page
of 1