Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia von Callea, M., Willoughby, C.E., Nieminen, P., Di Stazio, M., Bellacchio, E., Giglio, S., Sani, I., Vinciguerra, A., Maglione, M., Tadini, G., Clarich, G.

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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family von Callea, M., Nieminen, P., Willoughby, C.E., Clarich, G., Yavuz, I., Vinciguerra, A., Di Stazio, M., Giglio, S., Sani, I., Maglione, M., Pensiero, S., Tadini, G., Bellacchio, E.

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A case of Beckwith-Wiedemann syndrome with peculiar dental findings von Callea, M, Yavuz, I, Clarich, G, Gunay, A, Vinciguerra, A, Unal, M, Sahbaz, C, Sinan Dogan, M, Cammarata-Scalisi, F

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Oral manifestation of Goltz-Gorlin syndrome in a young girl von Callea, M, Yavuz, I, Deroma, L, Montanari, M, Clarich, G, Maglione, M, Albertini, E, Garavelli, L

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An evaluation of clinical, radiological and three-dimensional dental tomography findings in ectodermal dysplasia cases von Doğan, Mehmet-Sinan, Callea, Michele, Yavuz, Ìzzet, Aksoy, Orhan, Clarich, Gabriella, Günay, Ayse, Günay, Ahmet, Güven, Sedat, Maglione, Michele, Akkuş, Zeki

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Oral rehabilitation with implant-supported overdenture in a child with hypohidrotic ectodermal dysplasia von Montanari, M, Battelli, F, Callea, M, Corinaldesi, G, Sapigni, L, Marchetti, C, Tadini, G, Mancini, EG, Grecchi, F, Clarich, G, Salinas, CF, Fedele, G, Piana, G

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Testing for anti-human transglutaminase antibodies in saliva is not useful for diagnosis of celiac disease von Baldas, Valentina, Tommasini, Alberto, Santon, Daniela, Not, Tarcisio, Gerarduzzi, Tania, Clarich, Gabriella, Sblattero, Daniele, Marzari, Roberto, Florian, Fiorella, Martellossi, Stefano, Ventura, Alessandro

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Primary and secondary treatment in cleft lip and palate, our experience von Manna, F., Clarich, G., Radovich, F., Di Emidio, P., Pensiero, S., Riberti, C., Guarneri, G.F.

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A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family von Callea, M, Nieminen, P, Willoughby, C E, Clarich, G, Yavuz, I, Vinciguerra, A, Di Stazio, M, Giglio, S, Sani, I, Maglione, M, Pensiero, S, Tadini, G, Bellacchio, E

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