Zobrazeno 1 - 10
of 848
pro vyhledávání: '"Zelante, L"'
Publikováno v:
In Annales de genetique 2003 46(4):479-481
Publikováno v:
In Annales de genetique 2002 45(3):137-140
Autor:
Iolascon, A. *, Stewart, G.W., Ajetunmobi, J.F., Perrotta, S., Delaunay, J., Carella, M., Zelante, L., Gasparini, P.
Publikováno v:
In Blood 1 May 1999 93(9):3120-3123
Autor:
Bisceglia, L, Cerullo, G, Forabosco, P, Torres, Dd, Scolari, F, Di Perna, M, Foramitti, M, Amoroso, Antonio, Bertok, S, Floege, J, Mertens, Pr, Zerres, K, Alexopoulos, E, Kirmizis, D, Ermelinda, M, Zelante, L, Schena, Fp, European IgAN Consortium
Publikováno v:
American journal of human genetics 79 (2006): 1130–1134.
info:cnr-pdr/source/autori:Bisceglia L; Cerullo G; Forabosco P; Torres DD; Scolari F; Di Perna M; Foramitti M; Amoroso A; Bertok S; Floege J; Mertens PR; Zerres K; Alexopoulos E; Kirmizis D; Ermelinda M; Zelante L; Schena FP; European IgAN Consortium/titolo:Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci./doi:/rivista:American journal of human genetics/anno:2006/pagina_da:1130/pagina_a:1134/intervallo_pagine:1130–1134/volume:79
info:cnr-pdr/source/autori:Bisceglia L; Cerullo G; Forabosco P; Torres DD; Scolari F; Di Perna M; Foramitti M; Amoroso A; Bertok S; Floege J; Mertens PR; Zerres K; Alexopoulos E; Kirmizis D; Ermelinda M; Zelante L; Schena FP; European IgAN Consortium/titolo:Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci./doi:/rivista:American journal of human genetics/anno:2006/pagina_da:1130/pagina_a:1134/intervallo_pagine:1130–1134/volume:79
IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide, but its etiologic mechanisms are still poorly understood. Different prevalences among ethnic groups and familial aggregation, together with an increased familial risk, suggest im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ae23a2b055a133184303ec2ddca9618
Autor:
Feliubadaló, L., Font, M., Purroy, J., Rousaud, F., Estivill, X., Nunes, V., Golomb, E., Centola, M., Aksentijevich, I., Kreiss, Y., Goldman, B., Pras, M., Kastner, D. L., Pras, E., Gasparini, P., Bisceglia, L., Beccia, E., Gallucci, M., Sanctis, L. d., Ponzone, A., Rizzoni, G. F., Zelante, L., Bassi, M. T., George, A. L., Manzoni, Marta, Grandi, A. D., Riboni, M., Endsley, J. K., Ballabio, A., Borsani, Giuseppe, Reig, N., Fernández, E., Estévez, R., Pineda, M., Torrents, D., Camps, M., Lloberas, J., Zorzano, A., Palacín, M., Consortium, I. C.
Publikováno v:
Nature Genetics. 23:52-57
Cystinuria (MIM 220100) is a common recessive disorder of renal reabsorption of cystine and dibasic amino acids. Mutations in SLC3A1, encoding rBAT, cause cystinuria type I (ref. 1), but not other types of cystinuria (ref. 2). A gene whose mutation c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa82241235f90cdf0e979c8dd36936f5
https://doi.org/10.1038/12652
https://doi.org/10.1038/12652
Autor:
Savino, M, Borriello, A, Dapolito, M, Criscuolo, M, DEL VECCHIO, M, Bianco, Am, DI PERNA, M, Calzone, R, Nobili, B, Zatterale, A, Zelante, L, Joenje, H, DELLA RAGIONE, F, Savoia, A.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::365a77b5a72e7da4500dfabe8a0b76aa
http://hdl.handle.net/11368/1701486
http://hdl.handle.net/11368/1701486
Akademický článek
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Autor:
SERI M, SAVINO M, BORDO D, CUSANO R, MELONI I, MALATESTA P, CAPRIA M, PASI A. KOIVISTO PA, BOLOGNESI M, GHIGGERI GM, BALDUINI CL, ZELANTE L, RAVAZZOLO R, RENIERI A, SAVOIA, ANNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cba361edcdc44a81f5d6750fa51b1e56
http://hdl.handle.net/11368/1701499
http://hdl.handle.net/11368/1701499