Treatment outcomes maintained in Hunter syndrome patients: a case series on switching from idursulfase to idursulfase beta in Belarus

Anna Kulpanovich

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DOI: 10.1177/26330040261470451
Published: 2026-07
Container: Therapeutic Advances in Rare Disease
Publisher: SAGE Publications
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1177/26330040261470451,
  title = {Treatment outcomes maintained in Hunter syndrome patients: a case series on switching from idursulfase to idursulfase beta in Belarus},
  author = {Anna Kulpanovich},
  year = {2026},
  journal = {Therapeutic Advances in Rare Disease},
  doi = {10.1177/26330040261470451},
  url = {https://doi.org/10.1177/26330040261470451}
}

RIS

TY  - JOUR
TI  - Treatment outcomes maintained in Hunter syndrome patients: a case series on switching from idursulfase to idursulfase beta in Belarus
AU  - Anna Kulpanovich
PY  - 2026
JO  - Therapeutic Advances in Rare Disease
DO  - 10.1177/26330040261470451
UR  - https://doi.org/10.1177/26330040261470451
ER  -

APA

Kulpanovich, A. (2026). Treatment outcomes maintained in Hunter syndrome patients: a case series on switching from idursulfase to idursulfase beta in Belarus. Therapeutic Advances in Rare Disease. https://doi.org/10.1177/26330040261470451

Source records

crossref · retrieved 2026-09-27T02:29:41.363Z