Jameson E - Search Results

1

Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in England.

Broomfield A, Davison J, Roberts J, Stewart C, Hensman P, Beesley C, Tylee K, Rust S, Schwahn B, Jameson E, Vijay S, Santra S, Sreekantam S, Ramaswami U, Chakrapani A, Raiman J, Cleary MA, Jones SA. Broomfield A, et al. Among authors: jameson e. Mol Genet Metab. 2020 Feb;129(2):98-105. doi: 10.1016/j.ymgme.2019.07.016. Epub 2019 Jul 30. Mol Genet Metab. 2020. PMID: 31383595

2

Enzyme replacement therapy with laronidase (Aldurazyme^®) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Remmington T. Jameson E, et al. Cochrane Database Syst Rev. 2019 Jun 18;6(6):CD009354. doi: 10.1002/14651858.CD009354.pub5. Cochrane Database Syst Rev. 2019. PMID: 31211405 Free PMC article.

3

Outcomes of Long-Term Treatment with Laronidase in Patients with Mucopolysaccharidosis Type I.

Laraway S, Mercer J, Jameson E, Ashworth J, Hensman P, Jones SA. Laraway S, et al. Among authors: jameson e. J Pediatr. 2016 Nov;178:219-226.e1. doi: 10.1016/j.jpeds.2016.08.033. J Pediatr. 2016. PMID: 27788836 Free article.

4

Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Wraith JE. Jameson E, et al. Cochrane Database Syst Rev. 2013 Nov 21;(11):CD009354. doi: 10.1002/14651858.CD009354.pub3. Cochrane Database Syst Rev. 2013. Update in: Cochrane Database Syst Rev. 2016 Apr 01;4:CD009354. doi: 10.1002/14651858.CD009354.pub4 PMID: 24257962 Updated. Review.

5

Enzyme replacement therapy with laronidase (Aldurazyme(®)) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Remmington T. Jameson E, et al. Cochrane Database Syst Rev. 2016 Apr 1;4:CD009354. doi: 10.1002/14651858.CD009354.pub4. Cochrane Database Syst Rev. 2016. Update in: Cochrane Database Syst Rev. 2019 Jun 18;6:CD009354. doi: 10.1002/14651858.CD009354.pub5 PMID: 27033167 Updated. Review.

6

Expanding the phenotype in argininosuccinic aciduria: need for new therapies.

Baruteau J, Jameson E, Morris AA, Chakrapani A, Santra S, Vijay S, Kocadag H, Beesley CE, Grunewald S, Murphy E, Cleary M, Mundy H, Abulhoul L, Broomfield A, Lachmann R, Rahman Y, Robinson PH, MacPherson L, Foster K, Chong WK, Ridout DA, Bounford KM, Waddington SN, Mills PB, Gissen P, Davison JE. Baruteau J, et al. Among authors: jameson e. J Inherit Metab Dis. 2017 May;40(3):357-368. doi: 10.1007/s10545-017-0022-x. Epub 2017 Mar 1. J Inherit Metab Dis. 2017. PMID: 28251416 Free PMC article.

7

Enzyme replacement therapy with laronidase (Aldurazyme) for treating mucopolysaccharidosis type I.

Jameson E, Jones S, Wraith JE. Jameson E, et al. Cochrane Database Syst Rev. 2013 Sep 26;(9):CD009354. doi: 10.1002/14651858.CD009354.pub2. Cochrane Database Syst Rev. 2013. Update in: Cochrane Database Syst Rev. 2013 Nov 21;(11):CD009354. doi: 10.1002/14651858.CD009354.pub3 PMID: 24085657 Updated. Review.

8

Reversal of respiratory failure in both neonatal and late onset isolated remethylation disorders.

Broomfield A, Abulhoul L, Pitt W, Jameson E, Cleary M. Broomfield A, et al. Among authors: jameson e. JIMD Rep. 2014;16:51-6. doi: 10.1007/8904_2014_319. Epub 2014 Jul 6. JIMD Rep. 2014. PMID: 24997712 Free PMC article.

9

Diagnosing childhood-onset inborn errors of metabolism by next-generation sequencing.

Ghosh A, Schlecht H, Heptinstall LE, Bassett JK, Cartwright E, Bhaskar SS, Urquhart J, Broomfield A, Morris AA, Jameson E, Schwahn BC, Walter JH, Douzgou S, Murphy H, Hendriksz C, Sharma R, Wilcox G, Crushell E, Monavari AA, Martin R, Doolan A, Senniappan S, Ramsden SC, Jones SA, Banka S. Ghosh A, et al. Among authors: jameson e. Arch Dis Child. 2017 Nov;102(11):1019-1029. doi: 10.1136/archdischild-2017-312738. Epub 2017 May 3. Arch Dis Child. 2017. PMID: 28468868

10

Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease.

Oláhová M, Ceccatelli Berti C, Collier JJ, Alston CL, Jameson E, Jones SA, Edwards N, He L, Chinnery PF, Horvath R, Goffrini P, Taylor RW, Sayer JA. Oláhová M, et al. Among authors: jameson e. Hum Mol Genet. 2019 Nov 15;28(22):3766-3776. doi: 10.1093/hmg/ddz202. Hum Mol Genet. 2019. PMID: 31435670 Free PMC article.

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