Zobrazeno 1 - 10
of 394
pro vyhledávání: '"Pignatti, P F"'
Autor:
Muglia, P., Filosi, M., Ros, Da, Kam-Thong, T., Nardocci, F., Trabetti, E., Ratti, E., Rizzini, P., Zuddas, A., Bernardina, B. D., Domenici, Enrico, Alibrio, G., Anchisi, L., Andruccioli, M., Benvenuto, A., Battistella, P. A., Boscaini, F., Bravaccio, C., Ceppi, E., Cosentino, D., Curatolo, P., De Giacomo, A., Di Vita, G., Elia, M., Gitti, F., Grittani, S., Lamanna, A. L., Mani, E., Manzi, B., Margari, L., Masi, G., Molteni, M., Pascotto, A., Parmeggiani, A., Pignatti, P. F., Piroddi, T., Prandini, P., Russo, S., Scifo, R., Tancredi, R., Tiberti, A., Zoccante, L.
Publikováno v:
BMC Psychiatry
BMC Psychiatry, Vol 18, Iss 1, Pp 1-9 (2018)
BMC Psychiatry, Vol 18, Iss 1, Pp 1-9 (2018)
BackgroundA substantial genetic component accounts for Autism Spectrum Disorders (ASD) aetiology, with some rare and common genetic risk factors recently identified. Large collections of DNAs from thoroughly characterized ASD families are an essentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::152b19067c1aa54334e7c8891ee20dc3
http://europepmc.org/articles/PMC6247619
http://europepmc.org/articles/PMC6247619
Akademický článek
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Akademický článek
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Autor:
Malerba, Giovanni, Schaeffer, L., Xumerle, Luciano, Cavallari, Ugo Antonio Aristide, Klopp, N., Galavotti, Roberta, Trabetti, Elisabetta, Martinelli, Nicola, Biscuola, M., Guarini, Patrizia, Cavallari, U., Girelli, Domenico, Galavotti, R., Olivieri, Oliviero, Martinelli, N., Corrocher, Roberto, Guarini, P., Pignatti, Pierfranco, Girelli, D., Olivieri, O., Corrocher, R., Heinrich, J., Pignatti, P. F., Illig, T.
Publikováno v:
Lipids
Polymorphisms of the human Delta-5 (FADS1) and Delta-6 (FADS2) desaturase genes have been recently described to be associated with the level of several long-chain n-3 and n-6 polyunsaturated fatty acids (PUFAs) in serum phospholipids. We have genotyp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef5c61215bada9b264ae33539d95d3d9
https://doi.org/10.1007/s11745-008-3158-5
https://doi.org/10.1007/s11745-008-3158-5
Autor:
Mijatovic, V., Buson, G., Valenti, M. T., Dalle Carbonare, L., Ferrarini, A., Dal Molin, A., Mori, A., Xumerle, L., Caviola, E., Pertile, P., Delledonne, M., Pignatti, P. F., Malerba, G.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1943::0ceeb57eaab2b99d2b4e787675e63557
http://hdl.handle.net/11562/921194
http://hdl.handle.net/11562/921194
Autor:
Patuzzo, Cristina, Malerba, Giovanni, Xumerle, Luciano, Trabetti, Elisabetta, Galavotti, Roberta, Biscuola, M., Boner, Attilio, Galavotti, R., Pignatti, Pierfranco, Pescollderungg, L., Boner, A. L., Pignatti, P. F.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1943::2f9dc486a2dfb03df68812813d2b4d4d
http://hdl.handle.net/11562/389632
http://hdl.handle.net/11562/389632
Autor:
Alessandra Renieri, Bruttini, M., Galli, L., Zanelli, P., Neri, T., Rossetti, S., Turco, A., Heiskari, N., Zhou, J., Gusmano, R., Massella, L., Banfi, G., Scolari, F., Sessa, A., Rizzoni, G., Tryggvason, K., Pignatti, P. F., Savi, M., Ballabio, A., Marchi, M.
Publikováno v:
ResearcherID
Scopus-Elsevier
Scopus-Elsevier
The COL4A5 gene encodes the alpha5 (type IV) collagen chain and is defective in X-linked Alport syndrome (AS). Here, we report the first systematic analysis of all 51 exons of COL4A5 gene in a series of 201 Italian AS patients. We have previously rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f86886fd18922b60f39509f8c007d25f
http://hdl.handle.net/2318/38860
http://hdl.handle.net/2318/38860
Autor:
Alu', M, Asmundo, A, Carnevali, E, Cerri, N, Cortivo, P, Cucurachi, N, D'Aloja, E, DE FERRARI, F, DE STEFANO, F, DI NUNNO, C, Domenici, R, Fattorini, Paolo, Florian, Fiorella, Pappalardo, G, Pasqui, G, Peloso, G, Pelotti, S, Pignatti, P. F., Porfirio, B, Previdere', C, Ricci, U, Scimmi, D, Sciacca, G, Suadoni, F, Tagliabracci, A, Trabetti, E, Venturi, M.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::43bcfd6bee9dc0441f2dc942e2f397dc
https://hdl.handle.net/11368/1745263
https://hdl.handle.net/11368/1745263
Publikováno v:
European journal of human genetics : EJHG. 15(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4dc451e18c59c6e2852cc1b5cf864542
https://pubmed.ncbi.nlm.nih.gov/17180122
https://pubmed.ncbi.nlm.nih.gov/17180122
Autor:
Begnini, Angela, Trabetti, Elisabetta, Malerba, Giovanni, Bombieri, Cristina, Xumerle, Luciano, Galavotti, Roberta, Biscuola, M., Pignatti, Pierfranco, Galavotti, R., Pignatti, P. F.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1943::dd75be5db81a4e55b1f5e879f24c72a2
http://hdl.handle.net/11562/389508
http://hdl.handle.net/11562/389508