Yavuz I - Search Results

1

Ear nose throat manifestations in hypoidrotic ectodermal dysplasia.

Callea M, Teggi R, Yavuz I, Tadini G, Priolo M, Crovella S, Clarich G, Grasso DL. Callea M, et al. Among authors: yavuz i. Int J Pediatr Otorhinolaryngol. 2013 Nov;77(11):1801-4. doi: 10.1016/j.ijporl.2013.09.004. Epub 2013 Sep 13. Int J Pediatr Otorhinolaryngol. 2013. PMID: 24080322 Review.

2

[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. Among authors: yavuz i. 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.

3

[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. Among authors: yavuz i. 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.

4

A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family.

Callea M, Nieminen P, Willoughby CE, Clarich G, Yavuz I, Vinciguerra A, Di Stazio M, Giglio S, Sani I, Maglione M, Pensiero S, Tadini G, Bellacchio E. Callea M, et al. Among authors: yavuz i. J Eur Acad Dermatol Venereol. 2016 Feb;30(2):341-3. doi: 10.1111/jdv.12747. Epub 2014 Sep 30. J Eur Acad Dermatol Venereol. 2016. PMID: 25266272 No abstract available.

5

A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene.

Callea M, Fattori F, Yavuz I, Bertini E. Callea M, et al. Among authors: yavuz i. BMJ Case Rep. 2012 Dec 5;2012:bcr1220115422. doi: 10.1136/bcr-12-2011-5422. BMJ Case Rep. 2012. PMID: 23220435 Free PMC article.

6

An evaluation of clinical, radiological and three-dimensional dental tomography findings in ectodermal dysplasia cases.

Doğan MS, Callea M, Yavuz Ì, Aksoy O, Clarich G, Günay A, Günay A, Güven S, Maglione M, Akkuş Z. Doğan MS, et al. Among authors: yavuz i. Med Oral Patol Oral Cir Bucal. 2015 May 1;20(3):e340-6. doi: 10.4317/medoral.20303. Med Oral Patol Oral Cir Bucal. 2015. PMID: 25662550 Free PMC article.

7

A case of cleidocranial dysplasia with peculiar dental features: pathogenetic role of the RUNX2 mutation and long term follow-up.

Callea M, Bellacchio E, Di Stazio M, Fattori F, Bertini E, Yavuz I, Clarich G, Gunay A. Callea M, et al. Among authors: yavuz i. Oral Health Dent Manag. 2014 Jun;13(2):548-51. Oral Health Dent Manag. 2014. PMID: 24984680

8

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. Among authors: yavuz i. Eur J Paediatr Dent. 2016 Dec;17(4):315-317. Eur J Paediatr Dent. 2016. PMID: 28045321

9

[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. Among authors: yavuz i. 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.

10

A new biological approach to guided bone and tissue regeneration.

Montanari M, Callea M, Yavuz I, Maglione M. Montanari M, et al. Among authors: yavuz i. BMJ Case Rep. 2013 Apr 9;2013:bcr2012008240. doi: 10.1136/bcr-2012-008240. BMJ Case Rep. 2013. PMID: 23576648 Free PMC article.

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