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The Netherlands Journal of Medicine
|
May 31, 2018
Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levels
K F de Geus, A A Anas, R Franssen, et al.
Placenta
|
March 2, 2010
Analysis of placental tissue in Fabry disease with and without enzyme replacement therapy
M G Bouwman, C E M Hollak, M A van den Bergh Weerman, et al.
Journal of Inherited Metabolic Disease
|
June 2, 2017
Hearing loss in children with Fabry disease
E Suntjens, W A Dreschler, J Hess-Erga, et al.
The Netherlands Journal of Medicine
|
June 30, 2012
What contributes to internists' willingness to disclose medical errors?
G E Linthorst, B L Kallimanis-King, I Douwes Dekker, et al.
Molecular Genetics and Metabolism
|
November 11, 2009
Vasculopathy in patients with Fabry disease: current controversies and research directions
S M Rombach, Th B Twickler, J M F G Aerts, et al.
The British Journal of Dermatology
|
March 20, 2004
Misdiagnosis of Fabry disease: importance of biochemical confirmation of clinical or pathological suspicion
G E Linthorst, M A De Rie, K H Tjiam, et al.
The New England Journal of Medicine
|
July 7, 2001
Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease
C M Eng, N Guffon, W R Wilcox, et al.
Journal of Medical Genetics
|
October 3, 2009
Screening for Fabry disease in high-risk populations: a systematic review
G E Linthorst, M G Bouwman, F A Wijburg, et al.
Thrombosis and Haemostasis
|
July 15, 2000
Platelets release thrombopoietin (Tpo) upon activation: another regulatory loop in thrombocytopoiesis?
C C Folman, G E Linthorst, J van Mourik, et al.
Journal of Medical Genetics
|
August 8, 2013
A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance
L van der Tol, B E Smid, B J H M Poorthuis, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
The Netherlands Journal of Medicine
|
May 31, 2018
Congenital methaemoglobinaemia in a 61-year-old patient with normal haemoglobin levels
K F de Geus, A A Anas, R Franssen, et al.
Placenta
|
March 2, 2010
Analysis of placental tissue in Fabry disease with and without enzyme replacement therapy
M G Bouwman, C E M Hollak, M A van den Bergh Weerman, et al.
Journal of Inherited Metabolic Disease
|
June 2, 2017
Hearing loss in children with Fabry disease
E Suntjens, W A Dreschler, J Hess-Erga, et al.
The Netherlands Journal of Medicine
|
June 30, 2012
What contributes to internists' willingness to disclose medical errors?
G E Linthorst, B L Kallimanis-King, I Douwes Dekker, et al.
Molecular Genetics and Metabolism
|
November 11, 2009
Vasculopathy in patients with Fabry disease: current controversies and research directions
S M Rombach, Th B Twickler, J M F G Aerts, et al.
The British Journal of Dermatology
|
March 20, 2004
Misdiagnosis of Fabry disease: importance of biochemical confirmation of clinical or pathological suspicion
G E Linthorst, M A De Rie, K H Tjiam, et al.
The New England Journal of Medicine
|
July 7, 2001
Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease
C M Eng, N Guffon, W R Wilcox, et al.
Journal of Medical Genetics
|
October 3, 2009
Screening for Fabry disease in high-risk populations: a systematic review
G E Linthorst, M G Bouwman, F A Wijburg, et al.
Thrombosis and Haemostasis
|
July 15, 2000
Platelets release thrombopoietin (Tpo) upon activation: another regulatory loop in thrombocytopoiesis?
C C Folman, G E Linthorst, J van Mourik, et al.
Journal of Medical Genetics
|
August 8, 2013
A systematic review on screening for Fabry disease: prevalence of individuals with genetic variants of unknown significance
L van der Tol, B E Smid, B J H M Poorthuis, et al.
Page
of 3