Cox GF - Search Results

1

Childhood onset of Scheie syndrome, the attenuated form of mucopolysaccharidosis I.

Thomas JA, Beck M, Clarke JT, Cox GF. Thomas JA, et al. Among authors: cox gf. J Inherit Metab Dis. 2010 Aug;33(4):421-7. doi: 10.1007/s10545-010-9113-7. Epub 2010 Jun 2. J Inherit Metab Dis. 2010. PMID: 20532982 Free PMC article.

2

A dose-optimization trial of laronidase (Aldurazyme) in patients with mucopolysaccharidosis I.

Giugliani R, Rojas VM, Martins AM, Valadares ER, Clarke JT, Góes JE, Kakkis ED, Worden MA, Sidman M, Cox GF. Giugliani R, et al. Among authors: cox gf. Mol Genet Metab. 2009 Jan;96(1):13-9. doi: 10.1016/j.ymgme.2008.10.009. Epub 2008 Nov 26. Mol Genet Metab. 2009. PMID: 19038563 Clinical Trial.

3

Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I.

Clarke LA, Wraith JE, Beck M, Kolodny EH, Pastores GM, Muenzer J, Rapoport DM, Berger KI, Sidman M, Kakkis ED, Cox GF. Clarke LA, et al. Among authors: cox gf. Pediatrics. 2009 Jan;123(1):229-40. doi: 10.1542/peds.2007-3847. Pediatrics. 2009. PMID: 19117887 Clinical Trial.

4

Source document verification in the Mucopolysaccharidosis Type I Registry.

Verhulst K, Artiles-Carloni L, Beck M, Clarke JT, Neto JC, Cox GF, Fernhoff PM, Guffon N, Kong Y, Martins AM, Tylki-Szymanska A, Whitley CB, Wijburg FA, Wraith EJ, Koepper CM. Verhulst K, et al. Among authors: cox gf. Pharmacoepidemiol Drug Saf. 2012 Jul;21(7):749-752. doi: 10.1002/pds.2200. Epub 2011 Dec 14. Pharmacoepidemiol Drug Saf. 2012. PMID: 22170853

5

Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-L-iduronidase (laronidase).

Wraith JE, Clarke LA, Beck M, Kolodny EH, Pastores GM, Muenzer J, Rapoport DM, Berger KI, Swiedler SJ, Kakkis ED, Braakman T, Chadbourne E, Walton-Bowen K, Cox GF. Wraith JE, et al. Among authors: cox gf. J Pediatr. 2004 May;144(5):581-8. doi: 10.1016/j.jpeds.2004.01.046. J Pediatr. 2004. PMID: 15126990 Clinical Trial.

6

High rate of postoperative mortality in patients with mucopolysaccharidosis I: findings from the MPS I Registry.

Arn P, Whitley C, Wraith JE, Webb HW, Underhill L, Rangachari L, Cox GF. Arn P, et al. Among authors: cox gf. J Pediatr Surg. 2012 Mar;47(3):477-84. doi: 10.1016/j.jpedsurg.2011.09.042. J Pediatr Surg. 2012. PMID: 22424341

7

Physical performance testing in mucopolysaccharidosis I: a pilot study.

Dumas HM, Fragala MA, Haley SM, Skrinar AM, Wraith JE, Cox GF. Dumas HM, et al. Among authors: cox gf. Pediatr Rehabil. 2004 Apr-Jun;7(2):125-31. doi: 10.1080/13638490310001654763. Pediatr Rehabil. 2004. PMID: 15204583

8

Japan Elaprase Treatment (JET) study: idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (Mucopolysaccharidosis II, MPS II).

Okuyama T, Tanaka A, Suzuki Y, Ida H, Tanaka T, Cox GF, Eto Y, Orii T. Okuyama T, et al. Among authors: cox gf. Mol Genet Metab. 2010 Jan;99(1):18-25. doi: 10.1016/j.ymgme.2009.08.006. Mol Genet Metab. 2010. PMID: 19773189 Clinical Trial.

9

Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry.

D'Aco K, Underhill L, Rangachari L, Arn P, Cox GF, Giugliani R, Okuyama T, Wijburg F, Kaplan P. D'Aco K, et al. Among authors: cox gf. Eur J Pediatr. 2012 Jun;171(6):911-9. doi: 10.1007/s00431-011-1644-x. Epub 2012 Jan 11. Eur J Pediatr. 2012. PMID: 22234477 Free PMC article.

10

Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new cases.

Cassiman D, Packman S, Bembi B, Turkia HB, Al-Sayed M, Schiff M, Imrie J, Mabe P, Takahashi T, Mengel KE, Giugliani R, Cox GF. Cassiman D, et al. Among authors: cox gf. Mol Genet Metab. 2016 Jul;118(3):206-213. doi: 10.1016/j.ymgme.2016.05.001. Epub 2016 May 11. Mol Genet Metab. 2016. PMID: 27198631 Free article. Review.

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