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Dermatological findings in Rubinstein-Taybi Syndrome.
Cammarata-Scalisi F, Diociaiuti A, Cárdenas Tadich A, Sandoval X, Oranges T, Filippeschi C, Araya Castillo M, Willoughby CE, Cerri A, Gervasini C, Callea M. Cammarata-Scalisi F, et al. Among authors: cardenas tadich a. Ital J Dermatol Venerol. 2023 Aug;158(4):316-320. doi: 10.23736/S2784-8671.23.07547-3. Epub 2023 Jun 7. Ital J Dermatol Venerol. 2023. PMID: 37282850 Free article. Review.
Clinical, etiopathogenic, and therapeutic aspects of KID syndrome.
Cammarata-Scalisi F, Willoughby CE, Cárdenas Tadich A, Labrador N, Herrera A, Callea M. Cammarata-Scalisi F, et al. Among authors: cardenas tadich a. Dermatol Ther. 2020 Jul;33(4):e13507. doi: 10.1111/dth.13507. Epub 2020 Jul 4. Dermatol Ther. 2020. PMID: 32367610 Review.
Trisomy 21 and the coronavirus disease 2019 (COVID-19).
Cammarata-Scalisi F, Cárdenas Tadich A, Medina M, Callea M. Cammarata-Scalisi F, et al. Among authors: cardenas tadich a. Arch Argent Pediatr. 2020 Aug;118(4):230-231. doi: 10.5546/aap.2020.eng.230. Arch Argent Pediatr. 2020. PMID: 32677781 Free article. English, Spanish. No abstract available.
Genetic variability in the case of COVID-19 infection.
Cammarata-Scalisi F, Cárdenas Tadich A, Callea M. Cammarata-Scalisi F, et al. Among authors: cardenas tadich a. Arch Argent Pediatr. 2020 Oct;118(5):304-305. doi: 10.5546/aap.2020.eng.304. Arch Argent Pediatr. 2020. PMID: 32924391 Free article. English, Spanish. No abstract available.
A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1.
Cammarata-Scalisi F, Matysiak U, Willoughby CE, Ruzaike G, Cárdenas Tadich A, Araya Castillo M, Zara-Chirinos C, Bracho A, Avendaño A, Jilani H, Callea M. Cammarata-Scalisi F, et al. Among authors: cardenas tadich a. J Pediatr Genet. 2021 Jul 26;12(4):339-341. doi: 10.1055/s-0041-1732474. eCollection 2023 Dec. J Pediatr Genet. 2021. PMID: 38162154 Free PMC article.