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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.

  • 22 Similar Profiles
Skin Medicine & Life Sciences
Mutation Medicine & Life Sciences
Ichthyosis Medicine & Life Sciences
Ectodermal Dysplasia Medicine & Life Sciences
Nevus Medicine & Life Sciences
Epidermolysis Bullosa Dystrophica Medicine & Life Sciences
Epidermolysis Bullosa Medicine & Life Sciences
Junctional Epidermolysis Bullosa Medicine & Life Sciences

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Research Output 1982 2019

  • 3526 Citations
  • 30 h-Index
  • 148 Article
  • 2 Letter
  • 1 Chapter
  • 1 Review article

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., Jan 1 2019, In : Clinical Nutrition.

Research output: Contribution to journalReview article

Epidermolysis Bullosa
Nutritional Status
Mucous Membrane
Hand Deformities
Skin

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

Skin Neoplasms
Squamous Cell Carcinoma
Mutation
Poikiloderma of Kindler
Genes
2 Citations (Scopus)

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

Ectodermal Dysplasia
Genotype
Phenotype
Ectodysplasins
Tooth
2 Citations (Scopus)

Epidermolysis bullosa simplex–generalized severe type due to keratin 5 p.Glu477Lys mutation: Genotype-phenotype correlation and in silico modeling analysis

Lalor, L., Titeux, M., Palisson, F., Fuentes, I., Yubero, M. J., Tasanen, K., Huilaja, L., Has, C., Tadini, G., Haggstrom, A. N., Hovnanian, A. & Lucky, A. W., 2019, In : Pediatric Dermatology. 36, 1, p. 132-138

Research output: Contribution to journalArticle

Keratin-5
Epidermolysis Bullosa
Genetic Association Studies
Computer Simulation
Mutation

Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4

Ballin, N., Hotz, A., Bourrat, E., Küsel, J., Oji, V., Bouadjar, B., Brognoli, D., Hickman, G., Heinz, L., Vabres, P., Marrakchi, S., Leclerc-Mercier, S., Irvine, A., Tadini, G., Hamm, H., Has, C., Blume-Peytavi, U., Mitter, D., Reitenbach, M., Hausser, I. & 3 others, Zimmer, A. D., Alter, S. & Fischer, J., Jan 1 2019, (Accepted/In press) In : Human Mutation.

Research output: Contribution to journalArticle

Ichthyosis
Mutation
Mutation Rate
Genes
Phenotype