Hendriksz CJ - Search Results

1

The factors affecting lipid profile in adult patients with Mucopolysaccharidosis.

Stepien KM, Stewart FJ, Hendriksz CJ. Stepien KM, et al. Among authors: hendriksz cj. Mol Genet Metab Rep. 2017 May 18;12:35-40. doi: 10.1016/j.ymgmr.2017.05.006. eCollection 2017 Sep. Mol Genet Metab Rep. 2017. PMID: 28560179 Free PMC article.

2

Lipid profile in adult patients with Fabry disease - Ten-year follow up.

Stepien KM, Hendriksz CJ. Stepien KM, et al. Among authors: hendriksz cj. Mol Genet Metab Rep. 2017 Jul 13;13:3-6. doi: 10.1016/j.ymgmr.2017.06.010. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 28736719 Free PMC article.

3

Transition of patients with mucopolysaccharidosis from paediatric to adult care.

Lampe C, McNelly B, Gevorkian AK, Hendriksz CJ, Lobzhanidze TV, Pérez-López J, Stepien KM, Vashakmadze ND, Del Toro M. Lampe C, et al. Among authors: hendriksz cj. Mol Genet Metab Rep. 2019 Oct 21;21:100508. doi: 10.1016/j.ymgmr.2019.100508. eCollection 2019 Dec. Mol Genet Metab Rep. 2019. PMID: 31687335 Free PMC article.

4

Observational clinical study of 22 adult-onset Pompe disease patients undergoing enzyme replacement therapy over 5years.

Stepien KM, Hendriksz CJ, Roberts M, Sharma R. Stepien KM, et al. Among authors: hendriksz cj. Mol Genet Metab. 2016 Apr;117(4):413-8. doi: 10.1016/j.ymgme.2016.01.013. Epub 2016 Feb 4. Mol Genet Metab. 2016. PMID: 26873529

5

The use of port-a-caths in adult patients with Lysosomal Storage Disorders receiving Enzyme Replacement Therapy-one centre experience.

McLoughlin M, Stepien KM, McNelly B, Thompson L, Gorton J, Hendriksz CJ. McLoughlin M, et al. Among authors: hendriksz cj. Mol Genet Metab Rep. 2017 Oct 21;13:111-114. doi: 10.1016/j.ymgmr.2017.10.003. eCollection 2017 Dec. Mol Genet Metab Rep. 2017. PMID: 29071212 Free PMC article.

6

Cardiac rhythm abnormalities - An underestimated cardiovascular risk in adult patients with Mucopolysaccharidoses.

Ayuna A, Stepien KM, Hendriksz CJ, Balerdi M, Garg A, Woolfson P. Ayuna A, et al. Among authors: hendriksz cj. Mol Genet Metab. 2020 Jun;130(2):133-139. doi: 10.1016/j.ymgme.2020.03.005. Epub 2020 Mar 27. Mol Genet Metab. 2020. PMID: 32241717

7

Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy.

Noman K, Hendriksz CJ, Radcliffe G, Roncaroli F, Moreea S, Hussain A, Stepien KM. Noman K, et al. Among authors: hendriksz cj. Mol Genet Metab Rep. 2020 Sep 7;25:100646. doi: 10.1016/j.ymgmr.2020.100646. eCollection 2020 Dec. Mol Genet Metab Rep. 2020. PMID: 32963965 Free PMC article.

8

Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency--diagnostic difficulties and own experience in multidisciplinary management.

Stępień KM, Roberts M, Hendriksz CJ. Stępień KM, et al. Among authors: hendriksz cj. Dev Period Med. 2015 Oct-Dec;19(4):450-3. Dev Period Med. 2015. PMID: 26982752

9

The principles of the transition process from paediatric to adult services in inborn errors of metabolism--own experience.

Stępień KM, Hendriksz CJ. Stępień KM, et al. Among authors: hendriksz cj. Dev Period Med. 2015 Oct-Dec;19(4):523-7. Dev Period Med. 2015. PMID: 26982766

10

Long-term endurance and safety of elosulfase alfa enzyme replacement therapy in patients with Morquio A syndrome.

Hendriksz CJ, Parini R, AlSayed MD, Raiman J, Giugliani R, Solano Villarreal ML, Mitchell JJ, Burton BK, Guelbert N, Stewart F, Hughes DA, Berger KI, Slasor P, Matousek R, Jurecki E, Shaywitz AJ, Harmatz PR. Hendriksz CJ, et al. Mol Genet Metab. 2016 Sep;119(1-2):131-43. doi: 10.1016/j.ymgme.2016.05.018. Epub 2016 Jun 16. Mol Genet Metab. 2016. PMID: 27380995 Free article. Clinical Trial.

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