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pro vyhledávání: '"Olivia Sarah Strandbech"'
Publikováno v:
JIMD Reports, Vol 59, Iss 1, Pp 10-15 (2021)
Abstract Hypophosphatasia (HPP) is a rare inherited metabolic disorder characterized by deficient activity of alkaline phosphatase, causing defective mineralization of bones and teeth. The symptoms vary from no symptoms to stillbirth or skeletal mani
Externí odkaz:
https://doaj.org/article/31070a4fa3a24d09ab5ad48e0225c9e3
Publikováno v:
JIMD Reports
Strandbech, O S, Lund, A & Ostergaard, E 2021, ' Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia ', JIMD Reports, vol. 59, no. 1, pp. 10-15 . https://doi.org/10.1002/jmd2.12198
JIMD Reports, Vol 59, Iss 1, Pp 10-15 (2021)
Strandbech, O S, Lund, A & Ostergaard, E 2021, ' Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia ', JIMD Reports, vol. 59, no. 1, pp. 10-15 . https://doi.org/10.1002/jmd2.12198
JIMD Reports, Vol 59, Iss 1, Pp 10-15 (2021)
Hypophosphatasia (HPP) is a rare inherited metabolic disorder characterized by deficient activity of alkaline phosphatase, causing defective mineralization of bones and teeth. The symptoms vary from no symptoms to stillbirth or skeletal manifestation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66062c70b00dd99705da881c1f4194ef
http://europepmc.org/articles/PMC8100395
http://europepmc.org/articles/PMC8100395