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Fingerprint Dive into the research topics where Gianluca Tadini is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

A nutrition-based approach to epidermolysis bullosa: Causes, assessments, requirements and management

Salera, S., Tadini, G., Rossetti, D., Grassi, F. S., Marchisio, P., Agostoni, C., Giavoli, C., Rodari, G. & Guez, S., 2020, In : Clinical Nutrition. 39, 2, p. 343-352

Research output: Contribution to journalReview article

  • Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome

    Wang, H., Humbatova, A., Liu, Y., Qin, W., Lee, M., Cesarato, N., Kortüm, F., Kumar, S., Romano, M. T., Dai, S., Mo, R., Sivalingam, S., Motameny, S., Wu, Y., Wang, X., Niu, X., Geng, S., Bornholdt, D., Kroisel, P. M., Tadini, G. & 14 others, Walter, S. D., Hauck, F., Girisha, K. M., Calza, A. M., Bottani, A., Altmüller, J., Buness, A., Yang, S., Sun, X., Ma, L., Kutsche, K., Grzeschik, K. H., Betz, R. C. & Lin, Z., Jan 1 2020, (Accepted/In press) In : American Journal of Human Genetics.

    Research output: Contribution to journalArticle

  • Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

    Guerrero-Aspizua, S., Conti, C. J., Escamez, M. J., Castiglia, D., Zambruno, G., Youssefian, L., Vahidnezhad, H., Requena, L., Itin, P., Tadini, G., Yordanova, I., Martin, L., Uitto, J., Has, C. & Del Rio, M., Jul 24 2019, In : Orphanet Journal of Rare Diseases. 14, 1

    Research output: Contribution to journalArticle

  • Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients

    Guerrero-Aspizua, S., Conti, C. J., Escamez, M. J., Castiglia, D., Zambruno, G., Youssefian, L., Vahidnezhad, H., Requena, L., Itin, P., Tadini, G., Yordanova, I., Martin, L., Uitto, J., Has, C. & Del Rio, M., Jul 24 2019, In : Orphanet Journal of Rare Diseases. 14, 1, 183.

    Research output: Contribution to journalArticle

  • Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway

    Wright, J. T., Fete, M., Schneider, H., Zinser, M., Koster, M. I., Clarke, A. J., Hadj-Rabia, S., Tadini, G., Pagnan, N., Visinoni, A. F., Bergendal, B., Abbott, B., Fete, T., Stanford, C., Butcher, C., D'Souza, R. N., Sybert, V. P. & Morasso, M. I., Mar 1 2019, In : American Journal of Medical Genetics, Part A. 179, 3, p. 442-447 6 p.

    Research output: Contribution to journalArticle