Browsing by Author "Callea, M."
Now showing items 1-5 of 5
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A case of Beckwith-Wiedemann syndrome with peculiar dental findings
Callea, M.; Yavuz, I.; Clarich, G.; Gunay, A.; Vinciguerra, A.; Unal, M.; Sahbaz, C. (Ariesdue Srl, 2016)Background Beckwith-Wiedemann syndrome (BINS, OMIM 130650) is a rare genetic disorder characterised by overgrowth, tumor predisposition and congenital malformations. Few systemic manifestations and oral features have been ... -
Efficacy test of a toothpaste in reducing extrinsic dental stain
Agustanti, A.; Ramadhani, S. A.; Adiatman, M.; Rahardjo, A.; Callea, M.; Yavuz, I.; Maharani, D. A. (Iop Publishing Ltd, 2017)This clinical trial compared the external dental stain reduction achieved by tested toothpaste versus placebo in adult patients. In this double-blind, parallel, randomised clinical trial, 45 female volunteers with a mean ... -
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, C. E.; Clarich, G.; Yavuz, I.; Vinciguerra, A.; Di Stazio, M. (Wiley-Blackwell, 2016)[Abstract Not Available] -
Oral manifestation of Goltz-Gorlin syndrome in a young girl
Callea, M.; Yavuz, İzzet; Deroma, Laura; Montanari, Marco; Clarich, Gabriella; Maglione, Michele; Albertini, Enrico (BioMed Central Ltd., 2012)[No abstract available] -
Oral manifestations in a boy with X-linked reticulate pigmentary disorder
Callea, M.; Maglione, Michele; Yavuz, İzzet; Deroma, Laura; Willoughby, Colin E.; Tadini, Gianluca (BioMed Central Ltd., 2012)[No abstract available]
