9 results on '"Cassiman, David"'
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2. CLINICAL AND BIOCHEMICAL FOOTPRINTS OF INHERITED METABOLIC DISORDERS: A LESSON FROM THE KNOWLEDGEBASE
3. Overlapping and divergent hepatic and lipoprotein phenotypes in untreated adults with acid sphingomyelinase deficiency versus untreated adults with Gaucher disease from two pivotal clinical trials
4. Clinical and biochemical footprints of inherited metabolic diseases. II. Metabolic liver diseases
5. Corrigendum to “Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases” [Mol. Genet. Metab. 118 (2016) 206–213]
6. Renal involvement in PMM2-CDG, a mini-review
7. Disease severity scoring system for acid sphingomyelinase deficiency: Severity score domains and components
8. Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases
9. Cause of death in patients with attenuated acid sphingomyelinase deficiency: Comprehensive literature review and report of new cases
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