Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Cristiana Caprio"'
Autor:
Valeria Manfredini, Francesca Penagini, Francesca Di Nello, Chiara Cerini, Cristiana Caprio, Vania Giacomet, Giorgio Bedogni, Gian Vincenzo Zuccotti, Alessandra Viganò
Publikováno v:
Clinical Drug Investigation. 31:407-415
Background and Objective: Sporadic cases of renal toxicity have been reported in HIV-infected children treated with tenofovir disoproxil fumarate (TDF). We assessed the long-term renal safety of TDF in a cohort of vertically HIV-infected children, ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4f280d6ac3a645274cf9cc49908621b
https://doi.org/10.2165/11590400-000000000-00000
https://doi.org/10.2165/11590400-000000000-00000
T lymphocyte maturation is impaired in healthy young individuals carrying trisomy 21 (Down syndrome)
Autor:
Gian Vincenzo Zuccotti, Michela Pacei, Alessandra Viganò, Berardo di Natale, Laura Guazzarotti, Silvia Beretta, Luca Piacentini, Daria Trabattoni, Eleonora Castelletti, Cristiana Caprio, Mario Clerici, Piergiorgio Duca, Benedetta Boldrighini
Publikováno v:
American journal on intellectual and developmental disabilities. 114(2)
Cytokine production, immune activation, T lymphocytes maturation, and serum IL-7 concentration were examined in 24 youngsters with Down syndrome and no acquired diseases (healthy Down syndrome [12 prepubertal, 13 pubertal]) and 42 age- and gender-mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb09a03166cc427946bbf878165c1267
https://pubmed.ncbi.nlm.nih.gov/19391670
https://pubmed.ncbi.nlm.nih.gov/19391670
Autor:
M. Bosoni, Cristiana Caprio, Tuula Rinne, Silvia Mauri, Gian Vincenzo Zuccotti, Gian Luca Tadini, Giulia Pattarino, Hans van Bokhoven, Laura Guazzarotti
Publikováno v:
American Journal of Medical Genetics. Part A, 146A, 2001-4
American Journal of Medical Genetics. Part A, 146A, 15, pp. 2001-4
American Journal of Medical Genetics. Part A, 146A, 15, pp. 2001-4
We report on a case of a young women carrying an LMS typical phenotype associated with a severe dysgenesia of internal genitalia. The genotype, a 2-bp deletion (1576-1577DelTT) in exon 13 of the TP63 gene has been described, up to date, only in this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8decd0432f237eb944dad9b3b6286de
https://doi.org/10.1002/ajmg.a.32371
https://doi.org/10.1002/ajmg.a.32371
