المؤلفون: Pegoraro E, Gavassini BF, Benedetti S, Menditto I, Zara G, Padoan R, Mostacciuolo ML, Angelini C., FERRARI , MAURIZIO

المساهمون: Pegoraro, E, Gavassini, Bf, Benedetti, S, Menditto, I, Zara, G, Padoan, R, Mostacciuolo, Ml, Ferrari, Maurizio, Angelini, C.

مصطلحات موضوعية: dystrophin gene mutation, prenatal diagnosis

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000234313700007; volume:15:858-62; issue:12; firstpage:858; lastpage:862; numberofpages:5; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/20.500.11768/4892Test; http://dx.doi.org/10.1016/j.nmd.2005.08.008Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-28244452661

الإتاحة: https://doi.org/20.500.11768/4892Test
https://doi.org/10.1016/j.nmd.2005.08.008Test
https://hdl.handle.net/20.500.11768/4892Test

المؤلفون: ANDRIGO C, BOITO C, PRANDINI P, MOSTACCIUOLO ML, ANGELINI C, PEGORARO E., SICILIANO, GABRIELE

المساهمون: Andrigo, C, Boito, C, Prandini, P, Mostacciuolo, Ml, Siciliano, Gabriele, Angelini, C, Pegoraro, E.

وصف الملف: STAMPA

العلاقة: volume:6; firstpage:49; lastpage:50; numberofpages:2; journal:NEUROGENETICS; http://hdl.handle.net/11568/96421Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-15444381242

الإتاحة: http://hdl.handle.net/11568/96421Test

المؤلفون: ANGELINI C, MENEGAZZO E, MOSTACCIUOLO ML, MELACINI P, NOVELLI G, DALLAPICCOLA B., GENNARELLI, Massimo

المساهمون: Angelini, C, Menegazzo, E, Mostacciuolo, Ml, Melacini, P, Novelli, G, Gennarelli, Massimo, Dallapiccola, B.

العلاقة: ispartofbook:NEUROLOGY; 43th Annual Meting of the American Academy of Neurology; volume:43; firstpage:A413; lastpage:A413; http://hdl.handle.net/11379/80655Test

الإتاحة: http://hdl.handle.net/11379/80655Test

المؤلفون: VAZZA, GIOVANNI, Zortea M, Micaglio GF, Sartori V, Mostacciuolo ML, BOARETTO, FRANCESCA

المساهمون: Vazza, Giovanni, Zortea, M, Boaretto, Francesca, Micaglio, Gf, Sartori, V, Mostacciuolo, Ml

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/10877981; info:eu-repo/semantics/altIdentifier/wos/WOS:000089357800026; volume:67; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11577/2677460Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0033868486

الإتاحة: https://doi.org/10.1086/303017Test
http://hdl.handle.net/11577/2677460Test

المؤلفون: Mostacciuolo, ML, Pastorello, E, Vazza, G, Miorin, M, Angelini, C, Tomelleri, G, Galluzzi, G, Trevisan, CP

المصدر: Clinical Genetics ; volume 75, issue 6, page 550-555 ; ISSN 0009-9163 1399-0004

الإتاحة: https://doi.org/10.1111/j.1399-0004.2009.01158.xTest

المؤلفون: Saad FA, Mostacciuolo ML, Trevisan CP, Tomelleri G, Angelini C, Abdel Salam E, Danieli GA

المساهمون: Saad, Fa, Mostacciuolo, Ml, Trevisan, Cp, Tomelleri, G, Angelini, C, Abdel Salam, E, Danieli, Ga

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:A1997WK78500015; journal:HUMAN MUTATION; http://hdl.handle.net/11577/3355102Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0031000608

الإتاحة: http://hdl.handle.net/11577/3355102Test

المؤلفون: CAPON F, LEVATO C, MERLINI L, ANGELINI C, MOSTACCIUOLO ML, NOVELLI G, DALLAPICCOLA B., POLITANO, Luisa

المساهمون: Capon, F, Levato, C, Merlini, L, Angelini, C, Mostacciuolo, Ml, Politano, Luisa, Novelli, G, Dallapiccola, B.

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/8887955; info:eu-repo/semantics/altIdentifier/wos/WOS:A1996VK75400007; volume:6; firstpage:261; lastpage:264; numberofpages:4; journal:NEUROMUSCULAR DISORDERS; http://hdl.handle.net/11591/231099Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0030220199

الإتاحة: http://hdl.handle.net/11591/231099Test

المؤلفون: GENNARELLI, Massimo, NOVELLI G, ANDREASI BASSI F, MARTORELL L, CORNET M, MENEGAZZO E, MOSTACCIUOLO ML, MARTINEZ JM, ANGELINI C, PIZZUTI A, BAIGET M, DALLAPICCOLA B.

المساهمون: Gennarelli, Massimo, Novelli, G, ANDREASI BASSI, F, Martorell, L, Cornet, M, Menegazzo, E, Mostacciuolo, Ml, Martinez, Jm, Angelini, C, Pizzuti, A, Baiget, M, Dallapiccola, B.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:A1996VQ48400018; volume:65; firstpage:342; lastpage:347; journal:AMERICAN JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11379/5145Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0029807830

الإتاحة: http://hdl.handle.net/11379/5145Test

المؤلفون: Nelis E, Van Broeckhoven C, De Jonghe P, Löfgren A, Vandenberghe A, Latour P, Le Guern E, Brice A, Mostacciuolo ML, Schiavon F, Palau F, Bort S, Upadhyaya M, ROCCHI, Mariano, Mandich P, Bellone E, Silander K, Savontaus ML, Navon R, Goldberg Stern H, Estivill X, Volpini V, Friedl W, Gal A., ARCHIDIACONO, Nicoletta

المساهمون: Nelis, E, Van Broeckhoven, C, De Jonghe, P, Löfgren, A, Vandenberghe, A, Latour, P, Le Guern, E, Brice, A, Mostacciuolo, Ml, Schiavon, F, Palau, F, Bort, S, Upadhyaya, M, Rocchi, Mariano, Archidiacono, Nicoletta, Mandich, P, Bellone, E, Silander, K, Savontaus, Ml, Navon, R, Goldberg Stern, H, Estivill, X, Volpini, V, Friedl, W, Gal, A.

مصطلحات موضوعية: Hereditary Sensory and Motor Neuropathy/genetic, Mutation, Multigene Family

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:A1996UA94000006; volume:4; firstpage:25; lastpage:33; numberofpages:9; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11586/87164Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0029863589; http://www.ncbi.nlm.nih.gov/pubmed/8800924Test

الإتاحة: http://hdl.handle.net/11586/87164Test
http://www.ncbi.nlm.nih.gov/pubmed/8800924Test

المؤلفون: Schiavon F, Mostacciuolo ML, Saad F, Merlini L, Danieli G.A., SICILIANO, GABRIELE, ANGELINI, CARLO

المساهمون: Schiavon, F, Mostacciuolo, Ml, Saad, F, Merlini, L, Siciliano, Gabriele, Angelini, Carlo, Danieli, G. A.

العلاقة: volume:31; issue:11; firstpage:880; lastpage:883; numberofpages:4; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11568/24325Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0028032428

الإتاحة: http://hdl.handle.net/11568/24325Test