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of 23
pro vyhledávání: '"Bruno Letteria"'
Autor:
Calabrò Maria, Barberi Ignazio, La Mazza Antonella, Todaro Maria, De Luca Francesco L, Oreto Lilia, Russo Mario, Cerrito Marco, Bruno Letteria, Oreto Giuseppe
Publikováno v:
Italian Journal of Pediatrics, Vol 35, Iss 1, p 17 (2009)
Abstract Introduction The T wave is rarely bifid, apart from patients with long QT syndrome or subjects treated with antiarrhythmic drugs. At times, a U wave partially superimposed upon the T wave is responsible for an apparently bifid T wave. Bifid
Externí odkaz:
https://doaj.org/article/d370971b6c4049189c7deb7dca346f0f
Akademický článek
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Autor:
Caime, Flavia, Meo, Aurora Framcesca, De Luca, Francesco, Bruno, Letteria, Calabrò, Maria Pia, Gitto, Eloisa
Phelan-McDermid syndrome (PMS) or deletion 22q13 syndrome is a rare genetic syndrome resulting from loss of 22q13 region involving the SHANK3 gene. Main features are neonatal hypotonia, global developmental delay, absent to severely delayed speech an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4506ae483099f2924b2f1665dca30903
Autor:
Guerriero, Laura, Gagliano, Antonella, Lamberti, Marco, Calabro', Maria Pia, Siracusano, Rosamaria, Cigala, Virginia, Bartolone, M, De Luca, F., Bruno, Letteria, Spina, Edoardo, Germano', Eva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::016f45d1fd12d31e8864ce1257f544d1
http://hdl.handle.net/11570/2051837
http://hdl.handle.net/11570/2051837