Cammarata-Scalisi F - Search Results

1

Main genetic entities associated with supernumerary teeth.

Cammarata-Scalisi F, Avendaño A, Callea M. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2018 Dec 1;116(6):437-444. doi: 10.5546/aap.2018.eng.437. Arch Argent Pediatr. 2018. PMID: 30457727 Free article. Review. English, Spanish.

2

[Clinical and molecular study of the Noonan syndrome].

Cammarata-Scalisi F, Neri G, Pomponi MG, Mancano G, Da Silva G, Avendaño A, Lacruz-Rengel MA, Stock F, Sosa A. Cammarata-Scalisi F, et al. Invest Clin. 2012 Dec;53(4):395-401. Invest Clin. 2012. PMID: 23513489 Spanish.

3

[Double mutant alleles in the EXT1 gene not previously reported in a teenager with hereditary multiple exostoses].

Cammarata-Scalisi F, Cozar M, Grinberg D, Balcells S, Asteggiano CG, Martínez-Domenech G, Bracho A, Sánchez Y, Stock F, Delgado-Luengo W, Zara-Chirinos C, Chacín JA. Cammarata-Scalisi F, et al. Arch Argent Pediatr. 2015 Apr;113(2):e109-12. doi: 10.5546/aap.2015.e109. Arch Argent Pediatr. 2015. PMID: 25727835 Free article. Spanish.

4

[Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia].

Callea M, Yavuz I, Clarich G, Cammarata-Scalisi F. Callea M, et al. Arch Argent Pediatr. 2015 Dec 1;113(6):e341-4. doi: 10.5546/aap.2015.e341. Arch Argent Pediatr. 2015. PMID: 26593813 Free article. Spanish.

5

Acute myeloid leukemia in a 3 years old child with cleidocranial dysplasia.

Callea M, Bellacchio E, Fattori F, Bertini E, Callea F, Cammarata-Scalisi F. Callea M, et al. Leuk Lymphoma. 2016 Sep;57(9):2189-91. doi: 10.3109/10428194.2015.1115030. Epub 2015 Dec 24. Leuk Lymphoma. 2016. PMID: 26700323 No abstract available.

6

Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene.

Cammarata-Scalisi F, Natsuga K, Toyonaga E, Nishie W, Shimizu H, Avendaño A, Araque D, Da Silva G, Bellacchio E, Callea M. Cammarata-Scalisi F, et al. J Eur Acad Dermatol Venereol. 2017 Feb;31(2):e94-e96. doi: 10.1111/jdv.13800. Epub 2016 Jul 21. J Eur Acad Dermatol Venereol. 2017. PMID: 27445120 No abstract available.

7

A case of Beckwith-Wiedemann syndrome with peculiar dental findings.

Callea M, Yavuz I, Clarich G, Gunay A, Vinciguerra A, Unal M, Sahbaz C, Sinan Dogan M, Cammarata-Scalisi F. Callea M, et al. Eur J Paediatr Dent. 2016 Dec;17(4):315-317. Eur J Paediatr Dent. 2016. PMID: 28045321

8

Blood malignancies presenting with mutations at equivalent residues in RUNX1-2 suggest a common leukemogenic pathway.

Callea M, Fattori F, Bertini ES, Cammarata-Scalisi F, Callea F, Bellacchio E. Callea M, et al. Leuk Lymphoma. 2017 Aug;58(8):2002-2004. doi: 10.1080/10428194.2016.1274980. Epub 2017 Jan 16. Leuk Lymphoma. 2017. PMID: 28093006 No abstract available.

9

[Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia].

Callea M, Cammarata-Scalisi F, Willoughby CE, Giglio SR, Sani I, Bargiacchi S, Traficante G, Bellacchio E, Tadini G, Yavuz I, Galeotti A, Clarich G. Callea M, et al. Arch Argent Pediatr. 2017 Feb 1;115(1):e34-e38. doi: 10.5546/aap.2017.e34. Arch Argent Pediatr. 2017. PMID: 28097853 Free article. Spanish.

10

[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.

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