Successful pregnancy in a patient with multiple acyl-CoA dehydrogenase deficiency
Author:
Publisher
Elsevier BV
Subject
Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism
Reference7 articles.
1. Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency;Grünert;Orphanet J Rare Dis,2014
2. The metabolic and molecular bases of inherited disease;Frerman,2001
3. Glutaric acidaemia type II (multiple acyl-CoA dehydrogenation deficiency);Goodman;J Inherit Metab Dis,1984
4. Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency;Pollard;J Child Neurol,2010
5. Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment;Rosa;Eur J Paediatr Neurol,2012
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