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Journal of Inherited Metabolic Disease
|
February 22, 2020
Developments in the treatment of Fabry disease
Sanne J van der Veen, Carla E M Hollak, André B P van Kuilenburg, et al.
JIMD Reports
|
July 8, 2024
Riboflavin transporter deficiency in young adults unmasked by dietary changes
Bregje Jaeger, Mirjam Langeveld, Robert Brunkhorst, et al.
Heart (British Cardiac Society)
|
February 11, 2021
Influence of sex and phenotype on cardiac outcomes in patients with Fabry disease
Mohamed El Sayed, Alexander Hirsch, Matthijs Boekholdt, et al.
JIMD Reports
|
February 28, 2025
Treatment Beliefs Reflect Unmet Clinical Needs in Lysosomal Storage Diseases: An Opportunity for a Patient-Centered Approach
Eleonore M Corazolla, Mirjam Langeveld, Marion M M G Brands, et al.
Journal of Inherited Metabolic Disease
|
December 2, 2025
Sexual Dysfunction and Its Relationship With Hypogonadism and Myelopathy in Male Patients With X-Linked Adrenoleukodystrophy
Stephanie I W van de Stadt, Aimy M A Wessel, Mirjam Langeveld, et al.
Molecular Genetics and Metabolism
|
June 8, 2025
Fabry disease - a risk factor for renal cell cancer? - case series
Subadra Wanninayake, L van Dussen, Antonio Ochoa-Ferraro, et al.
Neonatology
|
September 19, 2022
Mind the B2: Life-Threatening Neonatal Complications of a Strict Vegan Diet during Pregnancy
Bregje Jaeger, Willemijn Corpeleijn, Monique Dijsselhof, et al.
JIMD Reports
|
September 14, 2022
Recurrent metabolic alkalosis following ketone body treatment of adult mitochondrial trifunctional protein deficiency: A case report
Nina N Stolwijk, Mirjam Langeveld, Bart A W Jacobs, et al.
Orphanet Journal of Rare Diseases
|
June 2, 2023
A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child
Lieke M van den Heuvel, Adriana Kater-Kuipers, Tessa van Dijk, et al.
Metabolism: Clinical and Experimental
|
February 13, 2007
Very low serum adiponectin levels in patients with type 1 Gaucher disease without overt hyperglycemia
Mirjam Langeveld, Saskia Scheij, Peter Dubbelhuis, et al.
Page
of 8
Search research articles
Search
Showing results (11-20 of 79) with videos related to
Sort By:
Page
of 8
Journal of Inherited Metabolic Disease
|
February 22, 2020
Developments in the treatment of Fabry disease
Sanne J van der Veen, Carla E M Hollak, André B P van Kuilenburg, et al.
JIMD Reports
|
July 8, 2024
Riboflavin transporter deficiency in young adults unmasked by dietary changes
Bregje Jaeger, Mirjam Langeveld, Robert Brunkhorst, et al.
Heart (British Cardiac Society)
|
February 11, 2021
Influence of sex and phenotype on cardiac outcomes in patients with Fabry disease
Mohamed El Sayed, Alexander Hirsch, Matthijs Boekholdt, et al.
JIMD Reports
|
February 28, 2025
Treatment Beliefs Reflect Unmet Clinical Needs in Lysosomal Storage Diseases: An Opportunity for a Patient-Centered Approach
Eleonore M Corazolla, Mirjam Langeveld, Marion M M G Brands, et al.
Journal of Inherited Metabolic Disease
|
December 2, 2025
Sexual Dysfunction and Its Relationship With Hypogonadism and Myelopathy in Male Patients With X-Linked Adrenoleukodystrophy
Stephanie I W van de Stadt, Aimy M A Wessel, Mirjam Langeveld, et al.
Molecular Genetics and Metabolism
|
June 8, 2025
Fabry disease - a risk factor for renal cell cancer? - case series
Subadra Wanninayake, L van Dussen, Antonio Ochoa-Ferraro, et al.
Neonatology
|
September 19, 2022
Mind the B2: Life-Threatening Neonatal Complications of a Strict Vegan Diet during Pregnancy
Bregje Jaeger, Willemijn Corpeleijn, Monique Dijsselhof, et al.
JIMD Reports
|
September 14, 2022
Recurrent metabolic alkalosis following ketone body treatment of adult mitochondrial trifunctional protein deficiency: A case report
Nina N Stolwijk, Mirjam Langeveld, Bart A W Jacobs, et al.
Orphanet Journal of Rare Diseases
|
June 2, 2023
A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child
Lieke M van den Heuvel, Adriana Kater-Kuipers, Tessa van Dijk, et al.
Metabolism: Clinical and Experimental
|
February 13, 2007
Very low serum adiponectin levels in patients with type 1 Gaucher disease without overt hyperglycemia
Mirjam Langeveld, Saskia Scheij, Peter Dubbelhuis, et al.
Page
of 8