Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Pecile V"'
Autor:
Dal Cin Sandro, Windischhofer Andreas, Pilat Florian, Leskowschek Michael, Pecile Vito F., David Mauro, Beiser Maximilian, Weih Robert, Koeth Johannes, Marschick Georg, Hinkov Borislav, Strasser Gottfried, Heckl Oliver H., Schwarz Benedikt
Publikováno v:
Nanophotonics, Vol 13, Iss 10, Pp 1759-1764 (2024)
Heterodyne detection based on interband cascade lasers (ICL) has been demonstrated in a wide range of different applications. However, it is still often limited to bulky tabletop systems using individual components such as dual laser setups, beam sha
Externí odkaz:
https://doaj.org/article/748efff6c7494f308b1e4819820a4322
Autor:
Monasta, L., Giangreco, M., Ancona, E., Barbone, F., Bet, E., Boschian-Bailo, P., Cacciaguerra, G., Cagnacci, A., Canton, M., Casarotto, M., Comar, M., Contardo, S., De Agostini, M., De Seta, F., Del Ben, G., Di Loreto, C., Driul, L., Facchin, S., Giornelli, R., Ianni, A., La Valle, S., Londero, A. P., Manfe, M., Maso, G., Mugittu, R., Olivuzzi, M., Orsaria, M., Pecile, V., Pinzano, R., Pirrone, F., Quadrifoglio, M., Ricci, G., Ronfani, L., Salviato, T., Sandrigo, E., Smiroldo, S., Sorz, A., Stampalija, T., Urriza, M., Vanin, M., Verardi, G., Alberico, S.
Publikováno v:
BMC Pregnancy and Childbirth
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-10 (2020)
BMC Pregnancy and Childbirth, Vol 20, Iss 1, Pp 1-10 (2020)
Background Intrauterine fetal death (IUFD) is a tragic event and, despite efforts to reduce rates, its incidence remains difficult to reduce. The objective of the present study was to examine the etiological factors that contribute to the main causes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64a48f30d60cfdc207ec01770ce70045
https://bmcpregnancychildbirth.biomedcentral.com/articles/10.1186/s12884-020-03074-9
https://bmcpregnancychildbirth.biomedcentral.com/articles/10.1186/s12884-020-03074-9
Akademický článek
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Autor:
Rocca, M. S.1, Pecile, V.2, Cleva, L.2, Speltra, E.1, Selice, R.1, Di Mambro, A.1, Foresta, C.1, Ferlin, A.1
Publikováno v:
Andrology. Mar2016, Vol. 4 Issue 2, p328-334. 7p.
Autor:
Colombo E, Locatelli A, Sanchez L, Romeo S, Elcioglu N, Maystadt I, Martinez A, Sironi A, Fontana L, Finelli P, Gervasini C, Pecile V, Larizza L
Publikováno v:
International Journal Of Molecular Sciences
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
instname
r-FIHGUV. Repositorio Institucional de Producción Científica de la Fundación de Investigación del Hospital General de Valencia
instname
Biallelic mutations in RECQL4 gene, a caretaker of the genome, cause Rothmund-Thomson type-II syndrome (RTS-II) and confer increased cancer risk if they damage the helicase domain. We describe five families exemplifying clinical and allelic heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::f23f1d2254ad2ef2bb6c6ee97c149138
https://fundanet.fihgu.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1177
https://fundanet.fihgu.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=1177
Akademický článek
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Akademický článek
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Autor:
Giardino, D, Corti, C, Ballarati, L, Colombo, D, Sala, E, Villa, N, Piombo, G, Pierluigi, M, Faravelli, F, Guerneri, S, Coviello, D, Lalatta, F, Cavallari, U, Bellotti, D, Barlati, Sergio, Croci, G, Franchi, F, Savin, E, Nocera, G, Amico, Fp, Granata, P, Casalone, R, Nutini, L, Lisi, E, Torricelli, F, Giussani, U, Facchinetti, B, Guanti, G, DI GIACOMO, M, Susca, Fp, Pecile, V, Romitti, L, Cardarelli, L, Racalbuto, E, Police, Ma, Chiodo, F, Rodeschini, O, Falcone, P, Donti, E, Grimoldi, Mg, Martinoli, E, Stioui, S, Caufin, D, Lauricella, Sa, Tanzariello, Sa, Voglino, G, Lenzini, E, Besozzi, M, Larizza, L, Dalprà, L.
Publikováno v:
Prenatal diagnosis. 29(3)
OBJECTIVE: We surveyed the datasheets of 29 laboratories concerning prenatal diagnosis of de novo apparently balanced chromosome rearrangements to assess the involvement of specific chromosomes, the breakpoints distribution and the impact on the preg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::928949598bb92b2c3badcd58f2aab413
https://pubmed.ncbi.nlm.nih.gov/19248039
https://pubmed.ncbi.nlm.nih.gov/19248039
Autor:
Bon, B.W.M. van, Koolen, D.A., Brueton, L., McMullan, D., Lichtenbelt, K.D., Ades, L.C., Peters, G., Gibson, K., Moloney, S., Novara, F., Pramparo, T., Bernardina, B. Dalla, Zoccante, L., Balottin, U., Piazza, F., Pecile, V., Gasparini, P., Guerci, V., Kets, M., Pfundt, R., Brouwer, A.P.M. de, Veltman, J.A., Leeuw, N. de, Wilson, M., Antony, J., Reitano, S., Luciano, D., Fichera, M., Romano, C, Brunner, H.G., Zuffardi, O., Vries, L.B.A. de
Publikováno v:
European Journal of Human Genetics, 18, 2, pp. 163-70
European Journal of Human Genetics, 18, 163-70
European Journal of Human Genetics, 18, 163-70
Contains fulltext : 89008.pdf (Publisher’s version ) (Closed access) Six submicroscopic deletions comprising chromosome band 2q23.1 in patients with severe mental retardation (MR), short stature, microcephaly and epilepsy have been reported, sugges
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325b0cdd6d84618af6b2d3e913c1aae8
https://hdl.handle.net/11368/3112
https://hdl.handle.net/11368/3112
Autor:
Disciglio, V, Rizzo, Cl, Mencarelli, Ma, Mucciolo, M, Marozza, A, Di Marco, C, Massarelli, A, Canocchi, V, Baldassarri, M, Ndoni, E, Frullanti, E, Amabile, S, Anderlid, Bm, Metcalfe, K, Caignec, Le, David, A, Fryer, A, Boute, O, Joris, A, Greco, D, Pecile, V, Battini, R, Novelli, A, Fichera, M, Romano, C, Mari, F, Renieri, A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3728::91f5198e1deca6d800ba638b28ece30b
http://hdl.handle.net/11568/951188
http://hdl.handle.net/11568/951188