A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis.
- DOI
- 10.24953/turkjpediatr.2026.6374
- Published
- 2026 Sep 11
- Container
- The Turkish journal of pediatrics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.24953/turkjpediatr.2026.6374,
title = {A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis.},
author = {Toprak Ş and Koral Ü and Alan S and Gülerman HF and Albayrak M},
year = {2026},
journal = {The Turkish journal of pediatrics},
doi = {10.24953/turkjpediatr.2026.6374},
url = {https://doi.org/10.24953/turkjpediatr.2026.6374}
}RIS
TY - JOUR TI - A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis. AU - Toprak Ş AU - Koral Ü AU - Alan S AU - Gülerman HF AU - Albayrak M PY - 2026 JO - The Turkish journal of pediatrics DO - 10.24953/turkjpediatr.2026.6374 UR - https://doi.org/10.24953/turkjpediatr.2026.6374 ER -
APA
Ş, T., Ü, K., S, A., HF, G., & M, A. (2026). A case of neonatal galactosemia presenting with rare hematologic problems: factor V deficiency and hemophagocytic lymphohistiocytosis.. The Turkish journal of pediatrics. https://doi.org/10.24953/turkjpediatr.2026.6374
Source records
- pubmed · retrieved 2026-09-26T16:04:04.712Z