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Journal of Inherited Metabolic Disease
|
June 9, 2020
Cognitive functioning and depressive symptoms in Fabry disease: A follow-up study
Simon Körver, Gert J Geurtsen, Carla E M Hollak, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 20, 2007
Type I Gaucher disease, a glycosphingolipid storage disorder, is associated with insulin resistance
Mirjam Langeveld, Karen J M Ghauharali, Hans P Sauerwein, et al.
Parkinsonism & Related Disorders
|
December 26, 2016
New insights in the neurological phenotype of aceruloplasminemia in Caucasian patients
Lena H P Vroegindeweij, Janneke G Langendonk, Mirjam Langeveld, et al.
Orphanet Journal of Rare Diseases
|
June 3, 2026
Treatment goals for adults with early treated PKU should be determined by evidence-based shared decision making between patients and their medical team
Mirjam Langeveld, Sandra Sirrs, Robin Lachman, et al.
Scientific Reports
|
January 19, 2019
Predictors of objective cognitive impairment and subjective cognitive complaints in patients with Fabry disease
Simon Körver, Gert J Geurtsen, Carla E M Hollak, et al.
Orphanet Journal of Rare Diseases
|
January 30, 2020
Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain
Simon Körver, Gert J Geurtsen, Carla E M Hollak, 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.
The American Journal of Clinical Nutrition
|
October 27, 2017
No metabolic effects of mustard allyl-isothiocyanate compared with placebo in men
Mirjam Langeveld, Chong Yew Tan, Maarten R Soeters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 23, 2020
Determinants of cerebral radiological progression in Fabry disease
Simon Körver, Maria G F Longo, Marjana R Lima, et al.
Orphanet Journal of Rare Diseases
|
October 4, 2024
Different diseases, different needs: Patient preferences for gene therapy in lysosomal storage disorders, a probabilistic threshold technique survey
Eleonore M Corazolla, Eline C B Eskes, Jorien Veldwijk, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 79) with videos related to
Sort By:
Page
of 8
Journal of Inherited Metabolic Disease
|
June 9, 2020
Cognitive functioning and depressive symptoms in Fabry disease: A follow-up study
Simon Körver, Gert J Geurtsen, Carla E M Hollak, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 20, 2007
Type I Gaucher disease, a glycosphingolipid storage disorder, is associated with insulin resistance
Mirjam Langeveld, Karen J M Ghauharali, Hans P Sauerwein, et al.
Parkinsonism & Related Disorders
|
December 26, 2016
New insights in the neurological phenotype of aceruloplasminemia in Caucasian patients
Lena H P Vroegindeweij, Janneke G Langendonk, Mirjam Langeveld, et al.
Orphanet Journal of Rare Diseases
|
June 3, 2026
Treatment goals for adults with early treated PKU should be determined by evidence-based shared decision making between patients and their medical team
Mirjam Langeveld, Sandra Sirrs, Robin Lachman, et al.
Scientific Reports
|
January 19, 2019
Predictors of objective cognitive impairment and subjective cognitive complaints in patients with Fabry disease
Simon Körver, Gert J Geurtsen, Carla E M Hollak, et al.
Orphanet Journal of Rare Diseases
|
January 30, 2020
Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain
Simon Körver, Gert J Geurtsen, Carla E M Hollak, 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.
The American Journal of Clinical Nutrition
|
October 27, 2017
No metabolic effects of mustard allyl-isothiocyanate compared with placebo in men
Mirjam Langeveld, Chong Yew Tan, Maarten R Soeters, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 23, 2020
Determinants of cerebral radiological progression in Fabry disease
Simon Körver, Maria G F Longo, Marjana R Lima, et al.
Orphanet Journal of Rare Diseases
|
October 4, 2024
Different diseases, different needs: Patient preferences for gene therapy in lysosomal storage disorders, a probabilistic threshold technique survey
Eleonore M Corazolla, Eline C B Eskes, Jorien Veldwijk, et al.
Page
of 8