ARTICULOS PUBMED
Montolío-Marzo S, González-Valdivia H, Casas-Gimeno E, Sebastian-Chapman L, Prat-Bartomeu J. Dermoid Cyst: Outcome Analysis in a Pediatric Referral Hospital. Ophthalmic Plast Reconstr Surg. 2020 Sep/Oct;36(5):478-480. doi: 10.1097/IOP.0000000000001608. PMID: 32205776.
Quiroz-Quiroga MJ, González Valdivia H, Palazón Cabanes A, Rubio Palau J, Prat Bartomeu J. Amblyopia due a dentigerous cyst. Case report and literature review. J Fr Ophtalmol. 2021 Oct;44(8):1249-1255. doi: 10.1016/j.jfo.2021.01.037. Epub 2021 Aug 2. PMID: 34353662.
https://www.sciencedirect.com/science/article/abs/pii/S0181551221003545?via%3Dihub
Franquesa-Garcia F, González-Valdivia H, Casas-Gimeno E, Rovira-Zurriag C, Prat-Bartomeu J. An Unusual Case of Lacrimal Gland Dacryops in a 10-Year-Old Child. J Pediatr Ophthalmol Strabismus. 2023 Nov-Dec;60(6):e79-e82. doi: 10.3928/01913913-20231026-02. Epub 2023 Nov 1. PMID: 38019941.
Palma-Carvajal F, González-Valdivia H, Figueroa-Vercellino JP, Saavedra-Gutiérrez C, Rovira-Zurriaga C, Prat-Bartomeu J. Optic pathway glioma with intraocular extension in a child with neurofibromatosis type-1. J Fr Ophtalmol. 2020 May;43(5):e179-e181. doi: 10.1016/j.jfo.2019.09.016. Epub 2020 Mar 30. PMID: 32241588.
https://www.sciencedirect.com/science/article/abs/pii/S0181551220301078?via%3Dihub
Montolío-Marzo S, Casas-Gimeno E, Prat-Bartomeu J. An Unusual Case of Unilateral Multiple Periorbital Dermoid Cyst. Ophthalmology. 2020 Mar;127(3):304. doi: 10.1016/j.ophtha.2019.12.010. PMID: 32087872.
https://www.sciencedirect.com/science/article/abs/pii/S0161642019323553?via%3Dihub
Fresno Cañada C, Gispets Parcerisas J, Del Prado Sánchez C, Puigventós Rosanas E, Perez-Jaume S, Salvador H, Llorca Cardeñosa A, Prat Bartomeu J. DRI Triton SS-OCT applied to detect choroidal nodules in paediatric patients affected by NF1. Heliyon. 2024 Apr 9;10(8):e29263. doi: 10.1016/j.heliyon.2024.e29263. PMID: 38644819; PMCID: PMC11033099.
https://www.sciencedirect.com/science/article/pii/S2405844024052940?via%3Dihub
Subirà O, Català-Mora J, Díaz-Cascajosa J, Padrón-Pérez N, Claveria MA, Coll-Alsina N, Bonnet C, Petit C, Caminal JM, Prat J. Retinal findings in pediatric patients with Usher syndrome Type 1 due to mutations in MYO7A gene. Eye (Lond). 2020 Mar;34(3):499-506. doi: 10.1038/s41433-019-0536-6. Epub 2019 Jul 18. PMID: 31320737; PMCID: PMC7042307.