Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Giovanni Battista Pozzan"'
Autor:
Onofrio Lamanna, Stefania Stefani, Viviana Cafiso, Michela Chirico, Giovanni Battista Pozzan, Flavia Baesso, Mario Cutrone, Lisa Bertoncello, Floriana Campanile, Pierluigi Brugnaro, Dafne Bongiorno, Stefano Grandesso, Sandra Mazzucato
Publikováno v:
Italian Journal of Pediatrics
Background The aims of this study were to identify the source and the transmission pathway for a Staphylococcal Scalded Skin Syndrome (SSSS) outbreak in a maternity setting in Italy over 2 months, during 2014; to implement appropriate control measure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c2262e4eee3f297a7e3202808a3781b
http://europepmc.org/articles/PMC5217574
http://europepmc.org/articles/PMC5217574
Autor:
Elisa Nalesso, Agostina De Crescenzo, Andrea Riccio, Paola Cavicchioli, Marilena Petrella, Angelo Selicorni, Barbara Zavan, Laura Cardarelli, Maria Vittoria Cubellis, Giovanni Battista Pozzan, Angela Sparago
Publikováno v:
Pediatric and developmental pathology
13 (2010): 326–330.
info:cnr-pdr/source/autori:Cardarelli L, Sparago A, De Crescenzo A, Nalesso E, Zavan B, Cubellis MV, Selicorni A, Cavicchioli P, Pozzan GB, Petrella M, Riccio A./titolo:Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single family/doi:/rivista:Pediatric and developmental pathology (Print)/anno:2010/pagina_da:326/pagina_a:330/intervallo_pagine:326–330/volume:13
13 (2010): 326–330.
info:cnr-pdr/source/autori:Cardarelli L, Sparago A, De Crescenzo A, Nalesso E, Zavan B, Cubellis MV, Selicorni A, Cavicchioli P, Pozzan GB, Petrella M, Riccio A./titolo:Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single family/doi:/rivista:Pediatric and developmental pathology (Print)/anno:2010/pagina_da:326/pagina_a:330/intervallo_pagine:326–330/volume:13
Genomic imprinting is an epigenetic phenomenon resulting in differential expression of maternal and paternal alleles of a subset of genes. In the mouse, mutation of imprinted genes often results in contrasting phenotypes, depending on parental origin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::447e2fc36ba1962762fc2027a577a2b2
http://hdl.handle.net/11591/190526
http://hdl.handle.net/11591/190526
Autor:
Pietro Maffei, Patsy M. Nishina, Cristina Maria Mihai, Isabelle Russell-Eggitt, Anne D. Nordstrom, Judy Davis, Sebastian Beck, Juergen K Naggert, Seamus Macdermott, Giovanni Battista Pozzan, Gayle B. Collin, Sarah Shea, Catherine Carey, Richard B Paisey, Nicola Sicolo, Maria Hoeltzenbein, Roderick T. Bronson, Jan D. Marshall, Ian Hopkinson, Gocha Shatirishvili
Background Alstrom syndrome is a recessively inherited genetic disorder characterized by congenital retinal dystrophy that leads to blindness, hearing impairment, childhood obesity, insulin resistance, and type 2 diabetes mellitus. We provide new det
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::831c8489dfb0e04c0b51a307c6efbf62
http://hdl.handle.net/11577/2473166
http://hdl.handle.net/11577/2473166