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Improvement in Bone Mineral Density and Architecture in a Patient with Gaucher Disease Using Teriparatide
Gaucher disease is an autosomal recessive lysosomal storage disorder caused by deficiency of the enzyme acid beta-glucosidase (glucocerebrosidase) due to mutations in the GBA gene. The most common form (type I) is associated with severe hematologic, visceral and bone disease. Disease-modifying treat...
Uloženo v:
| Vydáno v: | JIMD Rep |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer Berlin Heidelberg
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4486279/ https://ncbi.nlm.nih.gov/pubmed/25732996 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2015_407 |
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