Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Gian Luca Tadini"'
Autor:
Andrea Scaramuzza, Maddalena Macedoni, Gian Luca Tadini, Laura De Angelis, Francesca Redaelli, Alessandra Gazzarri, Valentina Comaschi, Elisa Giani, Gian Vincenzo Zuccotti
Publikováno v:
Case Reports in Pediatrics, Vol 2012 (2012)
Necrobiosis lipoidica is a rare disorder that usually appears in the lower extremities and it is often related to diabetes mellitus. There are few reported cases of necrobiosis lipoidica in children. We present an interesting case in that the patient
Externí odkaz:
https://doaj.org/article/7e4e2cf8dc3041fd9b128e76c8b49b8c
Autor:
Gian Vincenzo Zuccotti, A. Gazzarri, Andrea Scaramuzza, Gian Luca Tadini, Valentina Comaschi, Francesca Redaelli, Laura De Angelis, Maddalena Macedoni, Elisa Giani
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2012 (2012)
Case Reports in Pediatrics, Vol 2012 (2012)
Necrobiosis lipoidica is a rare disorder that usually appears in the lower extremities and it is often related to diabetes mellitus. There are few reported cases of necrobiosis lipoidica in children. We present an interesting case in that the patient
Autor:
Andrea Scaramuzza, Chiara Mameli, Gian Luca Tadini, Alessandra De Palma, Gian Vincenzo Zuccotti
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 164
Autor:
Chiara, Mameli, Andrea E, Scaramuzza, Gian Luca, Tadini, Sara, Riboni, Alessandra, De Palma, Gian Vincenzo, Zuccotti
Publikováno v:
Archives of pediatricsadolescent medicine. 163(7)
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
Autor:
Chiara Mameli, Andrea Scaramuzza, Alessandra De Palma, S. Riboni, Gian Luca Tadini, Gian Vincenzo Zuccotti
Publikováno v:
Archives of Pediatrics & Adolescent Medicine. 163:664
A N 11-YEAR-OLD ITALIAN BOY WITH TYPE 1 diabetes mellitus with onset in 2004 was brought to the Department of Pediatrics for a routine visit during which a large hemangioma in the left leg was observed (Figure, A). The hemangioma had been present sin