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The COVID-19 Pandemic and Enzyme Replacement Therapy in Lysosomal Storage Disorders
Download from doi.orgThe Evaluation of Skeletal Manifestations in Patients with Gaucher Disease
Download from doi.orgA case of glycogen storage disease type 1a mimicking familial chylomicronemia syndrome
Download from doi.orgGenotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemia
Download from link.springer.comAn unusual case of biotinidase deficiency with fingertip desquamation
Download from doi.orgLysinuric protein intolerance: an overlooked diagnosis
Download from link.springer.comBeneficial Effects of Modified Atkins Diet in Glycogen Storage Disease Type IIIa
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