Therapies for the bone in mucopolysaccharidoses

Patients with mucopolysaccharidoses (MPS) have accumulation of glycosaminoglycans in multiple tissues which may cause coarse facial features, mental retardation, recurrent ear and nose infections, inguinal and umbilical hernias, hepatosplenomegaly, and skeletal deformities. Clinical features related...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Mol Genet Metab
Prif Awduron: Tomatsu, Shunji, Alméciga-Díaz, Carlos J., Montaño, Adriana M., Yabe, Hiromasa, Tanaka, Akemi, Dung, Vu Chi, Giugliani, Roberto, Kubaski, Francyne, Mason, Robert W., Yasuda, Eriko, Sawamoto, Kazuki, Mackenzie, William, Suzuki, Yasuyuki, Orii, Kenji E., Barrera, Luis A., Sly, William S., Orii, Tadao
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2014
Pynciau:
Article
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4312706/
https://ncbi.nlm.nih.gov/pubmed/25537451
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2014.12.001
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