Zobrazeno 1 - 10
of 191
pro vyhledávání: '"Roggini M"'
Autor:
Giancotti, A., Castori, M., Lenzi, J., Manganaro, L., Papoff, P., Pizzuti, P., Polimeni, A., Roggini, M., Tarani, L., Silvestri, A., Cascone, Piero, Basile, Emanuela, Angeletti, Diletta, Vellone, Valentino, Ramieri, Valerio
Publikováno v:
In Journal of Cranio-Maxillo-Facial Surgery April 2016 44(4):493-499
Publikováno v:
Acta pædiatrica (Oslo) 100 (2011): 121–127. doi:10.1111/j.1651-2227.2010.01970.x
info:cnr-pdr/source/autori:Ruggieri, Martino; Roggini, Mario; Kennerknecht, Ingo; Polizzi, Agata; Distefano, Angela; Pavone, Vito/titolo:Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)/doi:10.1111%2Fj.1651-2227.2010.01970.x/rivista:Acta pædiatrica (Oslo)/anno:2011/pagina_da:121/pagina_a:127/intervallo_pagine:121–127/volume:100
info:cnr-pdr/source/autori:Ruggieri, Martino; Roggini, Mario; Kennerknecht, Ingo; Polizzi, Agata; Distefano, Angela; Pavone, Vito/titolo:Spectrum of skeletal abnormalities in a complex malformation syndrome with "cutis tricolor" (Ruggieri-Happle syndrome)/doi:10.1111%2Fj.1651-2227.2010.01970.x/rivista:Acta pædiatrica (Oslo)/anno:2011/pagina_da:121/pagina_a:127/intervallo_pagine:121–127/volume:100
The term cutis tricolor describes the combination of congenital hyper- and hypopigmented skin lesions in close proximity to each other in a background of normal complexion. This phenomenon has been reported: (i) as a purely cutaneous trait; (ii) as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5f58a163603e028fdf02b00d497b98ca
http://www.cnr.it/prodotto/i/305569
http://www.cnr.it/prodotto/i/305569
Autor:
Duse, Marzia, Indinnimeo, Luciana, Cutrera, R., DE CASTRO, Giovanna, Rossi, F. P., Quattrucci, S., Roggini, M., Villani, A., Zicari, Anna Maria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::ce8b91b38d353c0cbd30eb59ca7ce23e
http://hdl.handle.net/11573/231208
http://hdl.handle.net/11573/231208
Publikováno v:
Pediatric neurology 36 (2007): 407–410.
info:cnr-pdr/source/autori:Ruggieri M, Spalice A, Polizzi A, Roggini M, Iannetti P./titolo:Bilateral periventricular nodular heterotopia with amniotic band syndrome/doi:/rivista:Pediatric neurology/anno:2007/pagina_da:407/pagina_a:410/intervallo_pagine:407–410/volume:36
info:cnr-pdr/source/autori:Ruggieri M, Spalice A, Polizzi A, Roggini M, Iannetti P./titolo:Bilateral periventricular nodular heterotopia with amniotic band syndrome/doi:/rivista:Pediatric neurology/anno:2007/pagina_da:407/pagina_a:410/intervallo_pagine:407–410/volume:36
The amniotic (constriction) band syndrome is characterized by distal ring constrictions, intrauterine amputations, and acrosyndactyly. External constriction by amniotic bands is the generally accepted mechanism: early amniotic rupture leads to format
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::956186ec0548831cfeb1110b9609a4ce
http://www.cnr.it/prodotto/i/50053
http://www.cnr.it/prodotto/i/50053
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Akademický článek
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