Jones SA - Search Results

1

Outcome of haematopoietic cell transplantation in children with lysosomal acid lipase deficiency: a study on behalf of the EBMT Inborn Errors Working Party.

Lum SH, Minkov M, Jones SA, Hazelaar S, Sirait T, Potter JE, Stepensky P, Garban F, Pichler H, Stein J, Kaya Z, Schulz A, Mellgren K, Diaz de Heredia C, Pochon C, Riesco S, Diaz MA, Michel G, Lindemans C, Gruhn B, Albert MH, Lankester AC, Neven B, Wynn R. Lum SH, et al. Among authors: jones sa. Bone Marrow Transplant. 2023 May;58(5):594-596. doi: 10.1038/s41409-023-01918-4. Epub 2023 Feb 14. Bone Marrow Transplant. 2023. PMID: 36788366 No abstract available.

2

Changes in the incidence, patterns and outcomes of graft failure following hematopoietic stem cell transplantation for Hurler syndrome.

Lum SH, Miller WP, Jones S, Poulton K, Ogden W, Lee H, Logan A, Bonney D, Lund TC, Orchard PJ, Wynn RF. Lum SH, et al. Bone Marrow Transplant. 2017 Jun;52(6):846-853. doi: 10.1038/bmt.2017.5. Epub 2017 Feb 20. Bone Marrow Transplant. 2017. PMID: 28218755 Clinical Trial.

3

B-cell depletion abrogates immune mediated cytopenia and rejection of cord blood transplantation in Hurler syndrome.

Nataraj R, Hiwarkar P, Bonney D, Campbell H, Jones S, Deambrosis D, Evans P, Poulton K, van Hasselt PM, Bierings MB, Boelens JJ, Lindemans CA, Wynn R. Nataraj R, et al. Bone Marrow Transplant. 2022 Jan;57(1):38-42. doi: 10.1038/s41409-021-01465-w. Epub 2021 Oct 4. Bone Marrow Transplant. 2022. PMID: 34608276 Free PMC article.

4

A decade of excellent transplant survival in children with inherited metabolic diseases: A report from a single metabolic transplant centre in Europe.

Lum SH, Will A, Church HJ, Mercer J, Tylee KL, Poulton K, Odgen W, Lee H, Logan A, Coussons M, Khalid T, Bonney D, Rust S, Hiwarkar P, Jones SA, Wynn RF. Lum SH, et al. Among authors: jones sa. Blood Cell Ther. 2019 May 10;2(2):31-35. doi: 10.31547/bct-2018-012. eCollection 2019 May 10. Blood Cell Ther. 2019. PMID: 37885827 Free PMC article.

5

Hyperactive behaviour in the mouse model of mucopolysaccharidosis IIIB in the open field and home cage environments.

Langford-Smith A, Malinowska M, Langford-Smith KJ, Wegrzyn G, Jones S, Wynn R, Wraith JE, Wilkinson FL, Bigger BW. Langford-Smith A, et al. Genes Brain Behav. 2011 Aug;10(6):673-82. doi: 10.1111/j.1601-183X.2011.00706.x. Epub 2011 Jun 29. Genes Brain Behav. 2011. PMID: 21635693 Free article.

6

The evolution of pulmonary function in childhood onset Mucopolysaccharidosis type I.

Broomfield A, Sims J, Mercer J, Hensman P, Ghosh A, Tylee K, Stepien KM, Oldham A, Prathivadi Bhayankaram N, Wynn R, Wright NB, Jones SA, Wilkinson S. Broomfield A, et al. Among authors: jones sa. Mol Genet Metab. 2021 Feb;132(2):94-99. doi: 10.1016/j.ymgme.2020.07.004. Epub 2020 Jul 21. Mol Genet Metab. 2021. PMID: 32713717

7

Long-Term Cognitive and Functional Outcomes in Children with Mucopolysaccharidosis (MPS)-IH (Hurler Syndrome) Treated with Hematopoietic Cell Transplantation.

Kunin-Batson AS, Shapiro EG, Rudser KD, Lavery CA, Bjoraker KJ, Jones SA, Wynn RF, Vellodi A, Tolar J, Orchard PJ, Wraith JE. Kunin-Batson AS, et al. Among authors: jones sa. JIMD Rep. 2016;29:95-102. doi: 10.1007/8904_2015_521. Epub 2016 Jan 30. JIMD Rep. 2016. PMID: 26825088 Free PMC article.

8

"Why them, why me, why us?" The experiences of parents of children with lysosomal acid lipase deficiency: an interpretative phenomenological analysis study.

Hassall S, Smith DM, Rust S, Jones SA, Wittkowski A. Hassall S, et al. Among authors: jones sa. Orphanet J Rare Dis. 2022 May 12;17(1):193. doi: 10.1186/s13023-022-02335-4. Orphanet J Rare Dis. 2022. PMID: 35550173 Free PMC article.

9

A retrospective cohort study of Libmeldy (atidarsagene autotemcel) for MLD: What we have accomplished and what opportunities lie ahead.

Horgan C, Watts K, Ram D, Rust S, Hutton R, Jones S, Wynn R. Horgan C, et al. JIMD Rep. 2023 Jun 22;64(5):346-352. doi: 10.1002/jmd2.12378. eCollection 2023 Sep. JIMD Rep. 2023. PMID: 37701322 Free PMC article.

10

The impact of the immune system on the safety and efficiency of enzyme replacement therapy in lysosomal storage disorders.

Broomfield A, Jones SA, Hughes SM, Bigger BW. Broomfield A, et al. Among authors: jones sa. J Inherit Metab Dis. 2016 Jul;39(4):499-512. doi: 10.1007/s10545-016-9917-1. Epub 2016 Feb 16. J Inherit Metab Dis. 2016. PMID: 26883220 Review.

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