From FGFR3 Hyperactivation to Disease-Modifying Therapy in Pediatric Achondroplasia: Molecular Mechanisms, Clinical Evidence, and Emerging Treatments.

Șerban RC, Mitut-Veliscu A, Dumitra A, Marica L, Popescu C, Costache A, Teona Ș, Riza AL, Dirnu R, Varut RM, Streață I

Open source

DOI
10.3390/children13081121
Published
2026 Aug 21
Container
Children (Basel, Switzerland)
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.3390/children13081121,
  title = {From FGFR3 Hyperactivation to Disease-Modifying Therapy in Pediatric Achondroplasia: Molecular Mechanisms, Clinical Evidence, and Emerging Treatments.},
  author = {Șerban RC and Mitut-Veliscu A and Dumitra A and Marica L and Popescu C and Costache A and Teona Ș and Riza AL and Dirnu R and Varut RM and Streață I},
  year = {2026},
  journal = {Children (Basel, Switzerland)},
  doi = {10.3390/children13081121},
  url = {https://doi.org/10.3390/children13081121}
}

RIS

TY  - JOUR
TI  - From FGFR3 Hyperactivation to Disease-Modifying Therapy in Pediatric Achondroplasia: Molecular Mechanisms, Clinical Evidence, and Emerging Treatments.
AU  - Șerban RC
AU  - Mitut-Veliscu A
AU  - Dumitra A
AU  - Marica L
AU  - Popescu C
AU  - Costache A
AU  - Teona Ș
AU  - Riza AL
AU  - Dirnu R
AU  - Varut RM
AU  - Streață I
PY  - 2026
JO  - Children (Basel, Switzerland)
DO  - 10.3390/children13081121
UR  - https://doi.org/10.3390/children13081121
ER  - 

APA

RC, Ș., A, M., A, D., L, M., C, P., A, C., Ș, T., AL, R., R, D., RM, V., & I, S. (2026). From FGFR3 Hyperactivation to Disease-Modifying Therapy in Pediatric Achondroplasia: Molecular Mechanisms, Clinical Evidence, and Emerging Treatments.. Children (Basel, Switzerland). https://doi.org/10.3390/children13081121

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