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[Mosaic trisomy 18. Series of cases].
Cammarata-Scalisi F, Lacruz-Rengel MA, Araque D, Da Silva G, Avendaño A, Callea M, Stock F, Guerrero Y, Aguilar E, Lacruz MJ, Sulbaran J. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2017 Jun 1;115(3):e183-e186. doi: 10.5546/aap.2017.e183. Arch Argent Pediatr. 2017. PMID: 28504507 Free article. Spanish.
[Clinical and molecular study in a family with cleidocranial dysplasia].
Callea M, Fattori F, Bertini ES, Yavuz I, Bellacchio E, Avendaño A, Araque D, Lacruz-Rengel MA, Da Silva G, Cammarata-Scalisi F. Callea M, et al. Arch Argent Pediatr. 2017 Dec 1;115(6):e440-e444. doi: 10.5546/aap.2017.e440. Arch Argent Pediatr. 2017. PMID: 29087131 Free article. Spanish.
Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex.
Cammarata-Scalisi F, Vidales Moreno C, Stock F, Avendaño A, Araque D, Lacruz-Rengel MA, Diociaiuti A, Bellacchio E, Callea M. Cammarata-Scalisi F, et al. J Eur Acad Dermatol Venereol. 2018 Jun;32(6):e243-e245. doi: 10.1111/jdv.14765. Epub 2018 Feb 12. J Eur Acad Dermatol Venereol. 2018. PMID: 29265517 No abstract available.
[Isotretinoin embryopathy: An entity that can be avoided].
Cammarata-Scalisi F, Nieves D, Avendaño A, Lacruz-Rengel MA, Alviárez K, Dávila F, Yavuz I, Callea M. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2018 Apr 1;116(2):e303-e307. doi: 10.5546/aap.2018.e303. Arch Argent Pediatr. 2018. PMID: 29557621 Free article. Spanish.
68 results