يعرض 41 - 50 نتائج من 154 نتيجة بحث عن '"Vitelli, F."', وقت الاستعلام: 1.23s تنقيح النتائج
  1. 41
    دورية أكاديمية
    Mosaicism in Alport syndrome and genetic counseling.

    المؤلفون: BRUTTINI M., VITELLI F., MELONI, ILARIA, RIZZARI G., DELLA VOLPE M., MAZZUCCO G., DE MARCHI M., RENIERI, ALESSANDRA

    المساهمون: Bruttini, M., Vitelli, F., Meloni, Ilaria, Rizzari, G., DELLA VOLPE, M., Mazzucco, G., DE MARCHI, M., Renieri, Alessandra

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/11182935; info:eu-repo/semantics/altIdentifier/wos/WOS:000089298800019; volume:37; issue:9; firstpage:717; lastpage:719; numberofpages:3; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11365/17480Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033825031

    الإتاحة: https://doi.org/10.1136/jmg.37.9.717Test
    http://hdl.handle.net/11365/17480Test

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  2. 42
    دورية أكاديمية
    Identification and characterization of mouse orthologs of the AMMECR1 and FACL4 genes deleted in AMME syndrome: orthology of Xq22.3 and MmuXF1-F3.

    المؤلفون: VITELLI F, MELONI, ILARIA, FINESCHI S, FAVARA F, TIZIANA STORLAZZI C, ROCCHI M, RENIERI, ALESSANDRA

    المساهمون: Vitelli, F, Meloni, Ilaria, Fineschi, S, Favara, F, TIZIANA STORLAZZI, C, Rocchi, M, Renieri, Alessandra

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/10828604; info:eu-repo/semantics/altIdentifier/wos/WOS:000087351100024; volume:88; issue:3-4; firstpage:259; lastpage:263; numberofpages:5; journal:CYTOGENETICS AND CELL GENETICS; http://hdl.handle.net/11365/7359Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0034023784

    الإتاحة: https://doi.org/10.1159/000015533Test
    http://hdl.handle.net/11365/7359Test

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  3. 43
    دورية أكاديمية
    Identification and characterization of a highly conserved protein absent in the Alport S. (A), mental retardation (M), midface hypoplasia (M), and elliptocytosis (E) contiguous gene deletion syndrome

    المؤلفون: VITELLI, F., PICCINI, M., CAROLI, F., FRANCO, B., MALANDRINI, A., POBER, B., JONSSON, J., SORRENTINO, V., RENIERI, A.

    المساهمون: Vitelli, F., Piccini, M., Caroli, F., Franco, B., Malandrini, A., Pober, B., Jonsson, J., Sorrentino, V., Renieri, A.

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/10049589; info:eu-repo/semantics/altIdentifier/wos/WOS:000078771400011; volume:55; issue:3; firstpage:335; lastpage:340; numberofpages:6; journal:GENOMICS; http://hdl.handle.net/11365/38798Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033083073

    الإتاحة: https://doi.org/10.1006/geno.1998.5666Test
    http://hdl.handle.net/11365/38798Test

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  4. 44
    دورية أكاديمية
    KCNE1-like gene is deleted in AMME contiguous gene syndrome: identification and characterization of the human and mouse homologs

    المؤلفون: Piccini M, Vitelli F, Seri M, Galietta LJ, Moran O, Bulfone A, Pober B, Renieri A., BANFI, Sandro

    المساهمون: Piccini, M, Vitelli, F, Seri, M, Galietta, Lj, Moran, O, Bulfone, A, Banfi, Sandro, Pober, B, Renieri, A.

    العلاقة: volume:60; firstpage:251; lastpage:257; numberofpages:7; journal:GENOMICS; http://hdl.handle.net/11591/217721Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033568148

    الإتاحة: http://hdl.handle.net/11591/217721Test

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  5. 45
    دورية أكاديمية
    Relation of fibre intake to HbA1c and the prevalence of severe ketoacidosis and severe hypoglycaemia

    المؤلفون: Buyken A. E., Toeller M., Heitkamp G., Vitelli F., Stehle P., Scherbaum W. A., Fuller J. H., Cacciatori V., Bellavere F., Galante P., Gemma M. L., MUGGEO, Michele, BRANZI, Paola

    المساهمون: Buyken, A. E., Toeller, M., Heitkamp, G., Vitelli, F., Stehle, P., Scherbaum, W. A., Fuller, J. H., Muggeo, Michele, Cacciatori, V., Bellavere, F., Galante, P., Gemma, M. L., Branzi, Paola

    العلاقة: volume:41; firstpage:882; lastpage:890; numberofpages:9; journal:DIABETOLOGIA; http://hdl.handle.net/11562/12136Test

    الإتاحة: http://hdl.handle.net/11562/12136Test

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  6. 46
    دورية أكاديمية
    FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation

    المؤلفون: PICCINI M., VITELLI F., BRUTTINI M., POBER B. R., JONSSON J. J., VILLANOVA M., ZOLLO M., BORSANI G., BALLABIO A., RENIERI A.

    المساهمون: Piccini, M., Vitelli, F., Bruttini, M., Pober, B. R., Jonsson, J. J., Villanova, M., Zollo, M., Borsani, G., Ballabio, A., Renieri, A.

    وصف الملف: STAMPA

    العلاقة: info:eu-repo/semantics/altIdentifier/pmid/9480748; info:eu-repo/semantics/altIdentifier/wos/WOS:000072269800003; volume:47; issue:3; firstpage:350; lastpage:358; numberofpages:9; journal:GENOMICS; http://hdl.handle.net/11365/32939Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0032006885; https://www.sciencedirect.com/science/article/pii/S0888754397951041?via=ihubTest

    الإتاحة: https://doi.org/10.1006/geno.1997.5104Test
    http://hdl.handle.net/11365/32939Test
    https://www.sciencedirect.com/science/article/pii/S0888754397951041?via=ihubTest

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  7. 47
    دورية أكاديمية
    Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: a new X-linked contiguous gene deletion syndrome?

    المؤلفون: JONSSON J. J, RENIERI A, GALLAGHER P. G, KASHTAN C. E, CHERNISKI E. M, BRUTTINI M, PICCINI M, VITELLI F, POBER B. R., BALLABIO, ANDREA

    المساهمون: Jonsson, J. J., Renieri, A, Gallagher, P. G., Kashtan, C. E., Cherniski, E. M., Bruttini, M, Piccini, M, Vitelli, F, Ballabio, Andrea, Pober, B. R.

    العلاقة: volume:35; firstpage:273; lastpage:278; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11588/130679Test

    الإتاحة: http://hdl.handle.net/11588/130679Test

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  8. 48
    دورية أكاديمية
    FACL4, a new gene encoding Long-Chain Acyl-CoA Synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental retardation.

    المؤلفون: PICCINI M, VITELLI F, BRUTTINI M, POBER B. R, JONSSON J. J, VILLANOVA M, ZOLLO, MASSIMO, BORSANI G, RENIERI A., BALLABIO, ANDREA

    المساهمون: Piccini, M, Vitelli, F, Bruttini, M, Pober, B. R., Jonsson, J. J., Villanova, M, Zollo, Massimo, Borsani, G, Ballabio, Andrea, Renieri, A.

    العلاقة: volume:47; firstpage:350; lastpage:358; journal:GENOMICS; http://hdl.handle.net/11588/130681Test

    الإتاحة: http://hdl.handle.net/11588/130681Test

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  9. 49
    دورية أكاديمية
    Cardiovascular disease and its risk factors in IDDM in Europe

    المؤلفون: Koivisto VA, Stevens LK, Mattock M, Ebeling P, Muggeo M, Stephenson J, IdziorWalus B, Karamanos B, Tountas C, Kofinis A, Petrou K, Katsilambros N, Cignarelli M, Giorgino R, DeGeco ML, Ramunni I, IonescuTirgoviste C, Iosif CM, Pitei C, Buligescu S, Tamas G, Kerenyi Z, Ahmed AM, Toth J, Kempler P, Muntoni S, Songini M, Stabilini M, Fossarello M, Pintus S, Ferris B, Cronin CC, Toeller M, Klischan A, Forst T, Gries FA, Wagener W, Rottiers R, Priem H, Sinisalo M, Solnica B, SzopinskaCiba L, Solnica K, Krans M, Lemkes HHPJ, Jansen JJ, NunesCorrea J, Rogado C, Boavida JM, Correia LG, Michel G, Wirion R, Boulton AJM, Ashe H, Fernando DJS, Pozza G, Slaviero G, Comi B, Fattor F, Janka HU, Nuber A, Mehnert H, BenSoussan D, Fallas MC, Fallas P, Jepson E, McHardyYoung S, Fuller JH, Betteridge DJ, Milne M, Crepaldi C, Nosadini R, Cathelineau G, Cathelineau BV, Jellal M, Grodner N, Feiss PG, Santeusanio F, Rosi G, Cagini C, Marino C, Navalesi R, Penno G, Miccoli R, Nannipieri M, Stefano M, Ghirlanda G, Controneo P, Manto A, Teodonio C, Minnella A, Ward JD, Tesfaye S, Mody C, Rudd C, Molinatti GM, Vitelli F, Porta M, Pagano GF, Estivi P, Sivieri R, Carta Q, Petraroli G, Papazoglou N, Manes G, Triantaphyllou G, Ioannides A, Cacciatori V, Bellavere F, Galante P, Gemma ML, Irsigler K, Abrahamian H, Gurdet C, Hornlein B, Willinger C, Walford S, Wardle EV, Roglic G, Resman Z, Metelko Z, Skrabalo Z, Keen H, Sjolie AK, Viberti GC, Ward J, John G, Collins A, Sharp R., BANDELLO , FRANCESCO

    المساهمون: Koivisto, Va, Stevens, Lk, Mattock, M, Ebeling, P, Muggeo, M, Stephenson, J, Idziorwalus, B, Karamanos, B, Tountas, C, Kofinis, A, Petrou, K, Katsilambros, N, Cignarelli, M, Giorgino, R, Degeco, Ml, Ramunni, I, Ionescutirgoviste, C, Iosif, Cm, Pitei, C, Buligescu, S, Tamas, G, Kerenyi, Z, Ahmed, Am, Toth, J, Kempler, P, Muntoni, S, Songini, M, Stabilini, M, Fossarello, M, Pintus, S, Ferris, B, Cronin, Cc, Toeller, M, Klischan, A, Forst, T, Gries, Fa, Wagener, W, Rottiers, R, Priem, H, Sinisalo, M, Solnica, B, Szopinskaciba, L, Solnica, K, Krans, M, Lemkes, Hhpj, Jansen, Jj, Nunescorrea, J, Rogado, C, Boavida, Jm, Correia, Lg, Michel, G, Wirion, R, Boulton, Ajm, Ashe, H, Fernando, Dj, Pozza, G, Slaviero, G, Comi, B, Fattor, F, Bandello, Francesco, Janka, Hu, Nuber, A, Mehnert, H, Bensoussan, D, Fallas, Mc, Fallas, P, Jepson, E, Mchardyyoung, S, Fuller, Jh, Betteridge, Dj, Milne, M, Crepaldi, C, Nosadini, R, Cathelineau, G, Cathelineau, Bv, Jellal, M, Grodner, N, Feiss, Pg, Santeusanio, F, Rosi, G, Cagini, C, Marino, C, Navalesi, R, Penno, G, Miccoli, R, Nannipieri, M, Stefano, M, Ghirlanda, G, Controneo, P, Manto, A, Teodonio, C, Minnella, A, Ward, Jd, Tesfaye, S, Mody, C, Rudd, C, Molinatti, Gm, Vitelli, F, Porta, M, Pagano, Gf

    العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:A1996UT64600001; volume:19; issue:7; firstpage:689; lastpage:697; numberofpages:9; journal:DIABETES CARE; http://hdl.handle.net/20.500.11768/17736Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0029951345

    الإتاحة: https://doi.org/20.500.11768/17736Test
    https://doi.org/10.2337/diacare.19.7.689Test
    https://hdl.handle.net/20.500.11768/17736Test

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  10. 50
    دورية أكاديمية
    Confronto fra oftalmoscopia diretta e retinografia a colori nello screening della retinopatia diabetica

    المؤلفون: 2) Tomalino M, D'Addona GC, Minonne A, Passera P, Vitelli F, Montanaro M, TRENTO, Marina, PORTA, Massimo

    المساهمون: 2) Tomalino M, D'Addona GC, Minonne A, Trento M, Passera P, Vitelli F, Montanaro M, Porta M

    العلاقة: volume:16; firstpage:13; lastpage:16; journal:GIORNALE ITALIANO DI DIABETOLOGIA; http://hdl.handle.net/2318/77040Test

    الإتاحة: http://hdl.handle.net/2318/77040Test

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