Search Results (15)
Click the Why column to see why an item matched the search.
| Match | Type | Why |
|---|
| Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy. | Academic Article |
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| Glycogen Storage Disease Type I | Concept |
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| Glycogen Storage Disease Type II | Concept |
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| Glycogen Storage Disease Type IIb | Concept |
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| Glycogen Storage Disease Type III | Concept |
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| Glycogen Storage Disease Type IV | Concept |
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| Glycogen Storage Disease Type V | Concept |
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| Glycogen Storage Disease Type VI | Concept |
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| Glycogen Storage Disease Type VII | Concept |
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| Glycogen Storage Disease Type VIII | Concept |
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| Gannon, Jennifer | Person |
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| Enhancement of Newborn Screening Diagnostic Paradigms to Improve the Efficacy of Treatment for Krabbe Disease, Pompe Disease, and Mucopolysaccharidosis Type 1 | Grant |
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| An infant with pulmonary interstitial glycogenosis: clinical improvement is associated with improvement in the pulmonary diffusion capacity. | Academic Article |
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| Forsha, Daniel | Person |
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| Ehsan, Zarmina | Person |
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