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Challenges in Communicating a Genetic Diagnosis.
Cammarata-Scalisi F, Willoughby CE, Romano V, Callea M. Cammarata-Scalisi F, et al. Among authors: willoughby ce. Children (Basel). 2023 Mar 31;10(4):672. doi: 10.3390/children10040672. Children (Basel). 2023. PMID: 37189921 Free PMC article.
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: willoughby ce. Dermatol Ther. 2020 Jul;33(4):e13507. doi: 10.1111/dth.13507. Epub 2020 Jul 4. Dermatol Ther. 2020. PMID: 32367610 Review.
COVID-19 and ectodermal dysplasias. Recommendations are necessary.
Callea M, Willoughby CE, Perry D, Holzer U, Fedele G, Tadich AC, Cammarata-Scalisi F. Callea M, et al. Among authors: willoughby ce. Dermatol Ther. 2020 Sep;33(5):e13702. doi: 10.1111/dth.13702. Epub 2020 Jul 14. Dermatol Ther. 2020. PMID: 32475001 Free PMC article. No abstract available.
Membranous aplasia cutis congenita in trisomy 18.
Cammarata-Scalisi F, Diociaiuti A, de Guerrero B, Willoughby CE, Callea M. Cammarata-Scalisi F, et al. Among authors: willoughby ce. Ital J Pediatr. 2020 Aug 27;46(1):120. doi: 10.1186/s13052-020-00885-6. Ital J Pediatr. 2020. PMID: 32854736 Free PMC article.