SPECIALTY SCHOOL IN
MEDICAL GENETICS
UNIVERSITA' DEGLI STUDI DI SIENA
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Publications during the specialty course |
Castagnini Cinzia |
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Castagnini C, Luceri C, Toti S, Bigagli E, Caderni G, Femia AP, Giovannelli L, Lodovici M, Pitozzi V, Salvadori M, Messerini L, Martin R, Zoetendal EG, Gaj S, Eijssen L, Evelo CT, Renard CM, Baron A, Dolara P. Br J Nutr. 2009 Dec;102(11):1620-8. Epub 2009 Jul 22. |
2) Is complement alternative pathway disregulation involved in veno-occlusive disease of the liver? Bucalossi A, Toraldo F, Tozzi M, Lenoci M, Castagnini C, Artuso R, Renieri A, Marotta G. Biol Blood Marrow Transplant. 2010 Dec;16(12):1749-50. Epub 2010 Sep 19. |
3) An hystologically atypical NF-type 1 patient with a new pathogenic mutation. Bianco G, Greco G, Antonelli M, Casali S, Castagnini C. Neurological Sciences (in press) |
4) Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation. Bijlsma EK, Collins A, Papa FT, Tejada MI, Wheeler P, Peeters EA, Gijsbers AC, van de Kamp JM, Kriek M, Losekoot M, Broekma AJ, Crolla JA, Pollazzon M, Mucciolo M, Katzaki E, Disciglio V, Ferreri MI, Marozza A, Mencarelli MA, Castagnini C, Dosa L, Ariani F, Mari F, Canitano R, Hayek G, Botella MP, Gener B, Mínguez M, Renieri A, Ruivenkamp CA. Eur J Med Genet. 2012 Jun;55(6-7):404-13. Epub 2012 Mar 29 |