Zobrazeno 1 - 10
of 44
pro vyhledávání: '"VALLO L"'
Autor:
Vallo, L. (Leena)
Tutkielman tarkoituksena on selvittää kasvatusyhteistyön muotoja ja merkityksiä esiopetuksessa sekä alkuopetuksessa. Lisäksi tarkastellaan, kuinka kasvatusyhteistyö muuttuu esi- ja alkuopetuksen nivelvaiheessa, sekä kuinka vanhemmat kokevat k
Externí odkaz:
http://urn.fi/URN:NBN:fi:oulu-201705312248
Autor:
RINALDI F, BOTTA A, VALLO L, CONTINO G, MORGANTE A, IRACI R, CAVALLI C, SILVESTRI G, VENTRIGLIA VM, NOVELLI G., POLITANO, Luisa
Myotonic dystrophy type 1 (DM1) is the most frequently inherited neuromuscular disease in adults. It is a multisystemic disorder with major cardiac involvement most commonly represented by first-degree atrioventricular heart block (AVB), followed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3977::a5387aa48039a5abe6b4950ae7bf455f
http://hdl.handle.net/11591/233982
http://hdl.handle.net/11591/233982
Autor:
Rinaldi, F., Botta, A., Vallo, L., Contino, G., Morgante, A., Iraci, R., Claudio Catalli, Silvestri, G., Ventriglia, V. M., Politano, L., Novelli, G.
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Myotonic dystrophy type 1 (DM1) is the most frequently inherited neuromuscular disease in adults. It is a multisystemic disorder with major cardiac involvement most commonly represented by first-degree atrioventricular heart block (AVB), followed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::de7f66a634e83baaf5b638c9375d8fc6
http://hdl.handle.net/2108/10995
http://hdl.handle.net/2108/10995
Autor:
Veneziano L., Mantuano E., Spadaro M, Vallo L., Sabbadini G., DiGiacomo M., Jodice C., Frontali M.
Publikováno v:
8° congresso nazionale S.I.G.U., Chia laguna (SS), 2005
info:cnr-pdr/source/autori:Veneziano L., Mantuano E.,Spadaro M:, Vallo L., Sabbadini G., DiGiacomo M.,Jodice C., Frontali M./congresso_nome:8° congresso nazionale S.I.G.U./congresso_luogo:Chia laguna (SS)/congresso_data:2005/anno:2005/pagina_da:/pagina_a:/intervallo_pagine
info:cnr-pdr/source/autori:Veneziano L., Mantuano E.,Spadaro M:, Vallo L., Sabbadini G., DiGiacomo M.,Jodice C., Frontali M./congresso_nome:8° congresso nazionale S.I.G.U./congresso_luogo:Chia laguna (SS)/congresso_data:2005/anno:2005/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::e5aa36faff24ff0b1e3c2b963c8289af
https://publications.cnr.it/doc/98916
https://publications.cnr.it/doc/98916
Publikováno v:
Scopus-Elsevier
Myotonic dystrophy type 2 (DM2) lacks the expansion on chromosome 19q13 present in DM1 and is characterized by a mutation on 3q21. It has been shown that the DM2 mutation is a huge [CCTG]n repeat expansion in intron 1 of the zinc finger protein 9 (ZN
Autor:
Mostacciolo, Ml, Righetti, E, Zortea, M, Borsello, V, Schiavon, F, Vallo, L, Merlini, L, Siciliano, Gabriele, Fabrizi, Gm, Rizzuto, N, Dilani, M, Baratta, S, Tavoni, F.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3728::fec4b171a938a65ebdb22fcbe6f34513
http://hdl.handle.net/11568/67659
http://hdl.handle.net/11568/67659
Autor:
Mostacciuolo, MARIA LUISA, Righetti, E., Zortea, Michela, BOSELLO TRAVAIN, Valentina, Schiavon, F., Vallo, L., Merlini, L., Siciliano, G., Fabrizi, G. M., Rizzuto, N., Milani, M., Baratta, S. TARONI F.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3657::f66de9381d65d944b2f4dabbf3f17d3b
http://hdl.handle.net/11577/2457129
http://hdl.handle.net/11577/2457129
Publikováno v:
In Molecular and Cellular Probes 2005 19(1):71-74
Akademický článek
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