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You searched for: Author/Creator Mulder, Margot F.

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1. A nationwide retrospective observational study of population newborn screening for medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency in the Netherlands. Issue 5 (16th May 2019)

2. Clinical, biochemical, and molecular overview of transaldolase deficiency and evaluation of the endocrine function: Update of 34 patients. Issue 1 (11th February 2019)

3. Impact of newborn screening for very‐long‐chain acyl‐CoA dehydrogenase deficiency on genetic, enzymatic, and clinical outcomes. Issue 3 (8th April 2019)

4. Pain: a prevalent feature in patients with mucopolysaccharidosis. Results of a cross‐sectional national survey. Issue 2 (22nd July 2014)

5. Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency. Issue 1 (11th February 2019)

6. Retrospective evaluation of the Dutch pre‐newborn screening cohort for propionic acidemia and isolated methylmalonic acidemia: What to aim, expect, and evaluate from newborn screening?. Issue 3 (22nd December 2019)