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Critical clinical situations in adult patients with Mucopolysaccharidoses (MPS)

Abstract Background Mucopolysaccharidoses (MPS) are rare, inherited disorders associated with enzyme deficiencies that result in glycosaminoglycan (GAG) accumulation in multiple organ systems. Management of MPS is evolving as patients increasingly survive to adulthood and undergo multiple surgeries...

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Príomhchruthaitheoirí: Karolina M. Stepien, Anait K. Gevorkyan, Christian J. Hendriksz, Tinatin V. Lobzhanidze, Jordi Pérez-López, Govind Tol, Mireia del Toro Riera, Nato D. Vashakmadze, Christina Lampe
Formáid: Artigo
Teanga:Inglês
Foilsithe / Cruthaithe: BMC 2020-05-01
Sraith:Orphanet Journal of Rare Diseases
Ábhair:
Rochtain ar líne:http://link.springer.com/article/10.1186/s13023-020-01382-z
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