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1,276 results

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A phase II/III clinical study of enzyme replacement therapy with idursulfase in mucopolysaccharidosis II (Hunter syndrome).
Muenzer J, Wraith JE, Beck M, Giugliani R, Harmatz P, Eng CM, Vellodi A, Martin R, Ramaswami U, Gucsavas-Calikoglu M, Vijayaraghavan S, Wendt S, Puga AC, Ulbrich B, Shinawi M, Cleary M, Piper D, Conway AM, Kimura A. Muenzer J, et al. Among authors: cleary m. Genet Med. 2006 Aug;8(8):465-73. doi: 10.1097/01.gim.0000232477.37660.fb. Genet Med. 2006. PMID: 16912578 Free article. Clinical Trial.
Long-term, open-labeled extension study of idursulfase in the treatment of Hunter syndrome.
Muenzer J, Beck M, Eng CM, Giugliani R, Harmatz P, Martin R, Ramaswami U, Vellodi A, Wraith JE, Cleary M, Gucsavas-Calikoglu M, Puga AC, Shinawi M, Ulbrich B, Vijayaraghavan S, Wendt S, Conway AM, Rossi A, Whiteman DA, Kimura A. Muenzer J, et al. Among authors: cleary m. Genet Med. 2011 Feb;13(2):95-101. doi: 10.1097/GIM.0b013e3181fea459. Genet Med. 2011. PMID: 21150784 Free article. Clinical Trial.
Management of mucopolysaccharidosis type III.
Cleary MA, Wraith JE. Cleary MA, et al. Arch Dis Child. 1993 Sep;69(3):403-6. doi: 10.1136/adc.69.3.403. Arch Dis Child. 1993. PMID: 8215557 Free PMC article. Review. No abstract available.
Antenatal diagnosis of inborn errors of metabolism.
Cleary MA, Wraith JE. Cleary MA, et al. Arch Dis Child. 1991 Jul;66(7 Spec No):816-22. doi: 10.1136/adc.66.7_spec_no.816. Arch Dis Child. 1991. PMID: 1863132 Free PMC article. No abstract available.
Detection of inborn errors of metabolism in the newborn.
Chakrapani A, Cleary MA, Wraith JE. Chakrapani A, et al. Among authors: cleary ma. Arch Dis Child Fetal Neonatal Ed. 2001 May;84(3):F205-10. doi: 10.1136/fn.84.3.f205. Arch Dis Child Fetal Neonatal Ed. 2001. PMID: 11320051 Free PMC article. Review. No abstract available.
1,276 results