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Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I.
Riva M, Martorana D, Uliana V, Caleffi E, Boschi E, Garavelli L, Ponti G, Sangiorgi L, Graziano C, Bigoni S, Rocchetti LM, Madeo S, Soli F, Grosso E, Carli D, Goldoni M, Pisani F, Percesepe A. Riva M, et al. Among authors: ponti g. Genes Chromosomes Cancer. 2022 Jan;61(1):10-21. doi: 10.1002/gcc.22997. Epub 2021 Sep 3. Genes Chromosomes Cancer. 2022. PMID: 34427956 Free PMC article.
Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report.
Ponti G, Pellacani G, Tomasi A, Percesepe A, Guarneri C, Guerra A, Mandel VD, Kisla E, Cevikel P, Neri C, Menozzi C, Seidenari S. Ponti G, et al. J Med Case Rep. 2014 Oct 9;8:333. doi: 10.1186/1752-1947-8-333. J Med Case Rep. 2014. PMID: 25301139 Free PMC article.
Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas: role of clinical features, microsatellite instability, and immunohistochemistry.
Ponti G, Losi L, Di Gregorio C, Roncucci L, Pedroni M, Scarselli A, Benatti P, Seidenari S, Pellacani G, Lembo L, Rossi G, Marino M, Lucci-Cordisco E, Ponz de Leon M. Ponti G, et al. Cancer. 2005 Mar 1;103(5):1018-25. doi: 10.1002/cncr.20873. Cancer. 2005. PMID: 15662714 Free article.
198 results