Characterizing the frequency of clinical events and assessing biomarkers in propionic acidemia: a natural history study.

Schwahn BC, Berry GT, Vernon HJ, Li H, Merritt Ii JL, Schiff M, Chabrol B, De Las Heras J, Vockley J, Lee C, Koeberl DD, Burton BK, Grunewald S, Diaz GA, Ficicioglu C, Morgan T, Luo J, Attarwala H, Liang M, Perera S, Sikirica V

Open source

DOI
10.1186/s13023-026-04251-3
Published
2026 Mar 9
Container
Orphanet journal of rare diseases
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1186/s13023-026-04251-3,
  title = {Characterizing the frequency of clinical events and assessing biomarkers in propionic acidemia: a natural history study.},
  author = {Schwahn BC and Berry GT and Vernon HJ and Li H and Merritt Ii JL and Schiff M and Chabrol B and De Las Heras J and Vockley J and Lee C and Koeberl DD and Burton BK and Grunewald S and Diaz GA and Ficicioglu C and Morgan T and Luo J and Attarwala H and Liang M and Perera S and Sikirica V},
  year = {2026},
  journal = {Orphanet journal of rare diseases},
  doi = {10.1186/s13023-026-04251-3},
  url = {https://doi.org/10.1186/s13023-026-04251-3}
}

RIS

TY  - JOUR
TI  - Characterizing the frequency of clinical events and assessing biomarkers in propionic acidemia: a natural history study.
AU  - Schwahn BC
AU  - Berry GT
AU  - Vernon HJ
AU  - Li H
AU  - Merritt Ii JL
AU  - Schiff M
AU  - Chabrol B
AU  - De Las Heras J
AU  - Vockley J
AU  - Lee C
AU  - Koeberl DD
AU  - Burton BK
AU  - Grunewald S
AU  - Diaz GA
AU  - Ficicioglu C
AU  - Morgan T
AU  - Luo J
AU  - Attarwala H
AU  - Liang M
AU  - Perera S
AU  - Sikirica V
PY  - 2026
JO  - Orphanet journal of rare diseases
DO  - 10.1186/s13023-026-04251-3
UR  - https://doi.org/10.1186/s13023-026-04251-3
ER  - 

APA

BC, S., GT, B., HJ, V., H, L., JL, M. I., M, S., B, C., J, D. L. H., J, V., C, L., DD, K., BK, B., S, G., GA, D., C, F., T, M., J, L., H, A., M, L., S, P., & V, S. (2026). Characterizing the frequency of clinical events and assessing biomarkers in propionic acidemia: a natural history study.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-026-04251-3

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