المؤلفون: R. Dilena, J. C. Difrancesco, M. V. Soldovieri, A. Giacobbe, P. Ambrosino, I. Mosca, M. A. Galli, S. Guez, M. Fumagalli, F. Miceli, D. Cattaneo, F. Darra, E. Gennaro, F. Zara, P. Striano, B. Castellotti, C. Gellera, C. Varesio, P. Veggiotti, M. Taglialatela

المساهمون: R. Dilena, J.C. Difrancesco, M.V. Soldovieri, A. Giacobbe, P. Ambrosino, I. Mosca, M.A. Galli, S. Guez, M. Fumagalli, F. Miceli, D. Cattaneo, F. Darra, E. Gennaro, F. Zara, P. Striano, B. Castellotti, C. Gellera, C. Varesio, P. Veggiotti, M. Taglialatela

مصطلحات موضوعية: Developmental encephalopathy, Epilepsy of infancy with migrating focal seizures (EIMFS), KCNT1, Quinidine, Therapeutic drug monitoring (TDM), Settore MED/39 - Neuropsichiatria Infantile

Relation: info:eu-repo/semantics/altIdentifier/pmid/30112700; info:eu-repo/semantics/altIdentifier/wos/WOS:000452286500023; volume:15; issue:4; firstpage:1112; lastpage:1126; numberofpages:15; journal:NEUROTHERAPEUTICS; http://hdl.handle.net/2434/585322; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85052115388

الاتاحة: http://hdl.handle.net/2434/585322
https://doi.org/10.1007/s13311-018-0657-9

المؤلفون: TILOCA, CINZIA, N. Ticozzi, V. Pensato, L. Corrado, R. Del Bo, C. Bertolin, C. Fenoglio, S. Gagliardi, D. Calini, G. Lauria, B. Castellotti, A. Bagarotti, S. Corti, D. Galimberti, A. Cagnin, C. Gabelli, M. Ranieri, M. Ceroni, G. Siciliano, L. Mazzini, C. Cereda, E. Scarpini, G. Sorarù, G.P. Comi, S. D'Alfonso, C. Gellera, A. Ratti, J. E. Landers, V. Silani

المساهمون: T. Cinzia, N. Ticozzi, V. Pensato, L. Corrado, R. Del Bo, C. Bertolin, C. Fenoglio, S. Gagliardi, D. Calini, G. Lauria, B. Castellotti, A. Bagarotti, S. Corti, D. Galimberti, A. Cagnin, C. Gabelli, M. Ranieri, M. Ceroni, G. Siciliano, L. Mazzini, C. Cereda, E. Scarpini, G. Sorarù, G.P. Comi, S. D'Alfonso, C. Gellera, A. Ratti, J.E. Lander, V. Silani

مصطلحات موضوعية: amyotrophic lateral sclerosi, frontotemporal dementia, profilin 1, mutation analysis, Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica, Settore MED/03 - Genetica Medica

Relation: info:eu-repo/semantics/altIdentifier/pmid/23063648; info:eu-repo/semantics/altIdentifier/wos/WOS:000315729500024; volume:34; issue:5; firstpage:1517.e9; lastpage:1517.e10; numberofpages:2; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2434/208417; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84873434999

الاتاحة: http://hdl.handle.net/2434/208417
https://doi.org/10.1016/j.neurobiolaging.2012.09.016

المؤلفون: D. Calini, L. Corrado, R. Del Bo, S. Gagliardi, V. Pensato, F. Verde, S. Corti, L. Mazzini, P. Milani, B. Castellotti, C. Bertolin, G. Sorarù, C. Cereda, G.P. Comi, S. D'Alfonso, C. Gellera, N. Ticozzi, J. E. Landers, A. Ratti, V. Silani

المساهمون: D. Calini, L. Corrado, R. Del Bo, S. Gagliardi, V. Pensato, F. Verde, S. Corti, L. Mazzini, P. Milani, B. Castellotti, C. Bertolin, G. Sorarù, C. Cereda, G.P. Comi, S. D'Alfonso, C. Gellera, N. Ticozzi, J.E. Lander, A. Ratti, V. Silani

مصطلحات موضوعية: ALS, Genetic, hnRNP, Prion-like domain, IBMPFD, Settore MED/26 - Neurologia, Settore BIO/11 - Biologia Molecolare

Relation: info:eu-repo/semantics/altIdentifier/pmid/23827524; info:eu-repo/semantics/altIdentifier/wos/WOS:000324124000032; volume:34; issue:11; firstpage:2695.e11; lastpage:2695.e12; numberofpages:2; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2434/225540; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84881555711

الاتاحة: http://hdl.handle.net/2434/225540
https://doi.org/10.1016/j.neurobiolaging.2013.05.025

المؤلفون: E. Salsano, B. Castellotti, C. Gellera, M. Rimoldi, V. Pensato, C. Mariotti, D. Pareyson, G. Uziel, S. Tabano, S.M. Sirchia, P. Colapietro, M. Miozzo

المساهمون: E. Salsano, S. Tabano, S.M. Sirchia, P. Colapietro, B. Castellotti, C. Gellera, M. Rimoldi, V. Pensato, C. Mariotti, D. Pareyson, M. Miozzo, G. Uziel

مصطلحات موضوعية: Settore MED/03 - Genetica Medica, Settore MED/26 - Neurologia

Relation: info:eu-repo/semantics/altIdentifier/pmid/22280810; info:eu-repo/semantics/altIdentifier/wos/WOS:000301584500001; volume:7; issue:10; firstpage:10-1; lastpage:10-9; journal:ORPHANET JOURNAL OF RARE DISEASES; http://hdl.handle.net/2434/175984; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84856091180; http://www.ojrd.com/content/7/1/10

الاتاحة: http://hdl.handle.net/2434/175984
https://doi.org/10.1186/1750-1172-7-10
http://www.ojrd.com/content/7/1/10

المؤلفون: S, Groeneweg, FS, van Geest, A, Abacı, A, Alcantud, GP, Ambegaonkar, CM, Armour, P, Bakhtiani, D, Barca, ES, Bertini, IM, van Beynum, N, Brunetti-Pierri, M, Bugiani, M, Cappa, G, Cappuccio, B, Castellotti, C, Castiglioni, K, Chatterjee, IFM, de Coo, R, Coutant, D, Craiu, P, Crock, C, DeGoede, K, Demir, A, Dica, P, Dimitri, A, Dolcetta-Capuzzo, MHG, Dremmen, R, Dubey, A, Enderli, J, Fairchild, J, Gallichan, B, George, EF, Gevers, A, Hackenberg, Z, Halasz, B, Heinrich, T, Huynh, A, Kłosowska, MS, van der Knaap, MM, van der Knoop, D, Konrad, DA, Koolen, H, Krude, A, Lawson-Yuen, J, Lebl, M, Linder-Lucht, CF, Lorea, CM, Lourenco, RJ, Lunsing, G, Lyons

المصدر: Yearbook of Paediatric Endocrinology ; ISSN 1662-4009

الاتاحة: http://dx.doi.org/10.1530/ey.18.3.13
http://www.espeyearbook.org/ey/0018/ey0018.3-13.htm

المؤلفون: I. Fogh, A. Ratti, C. Gellera, K. Lin, C. Tiloca, V. Moskvina, L. Corrado, G. Sorarù, C. Cereda, S. Corti, D. Gentilini, D. Calini, B. Castellotti, L. Mazzini, G. Querin, S. Gagliardi, R. D. Bo, F. L. Conforti, G. Siciliano, M. Inghilleri, Francesco Saccà, P. Bongioanni, S. Penco, M. Corbo, S. Sorbi, M. Filosto, A. Ferlini, A. M. Di, S. Signorini, A. Shatunov, A. Jones, P. J. Shaw, K. E. Morrison, A. E. Farmer, P. V. Damme, W. Robberecht, A. Chiò, B. J. Traynor, M. Sendtner, J. Melki, V. Meininger, O. Hardiman, P. M. Andersen, N. P. Leigh, J. D. Glass, D. Overste, F. P. Diekstra, J. H. Veldink, M. A. van, C. E. Shaw, M. E. Weale, C. M. Lewis, J. Williams, R. H. Brown, J. E. Landers, N. Ticozzi, M. Ceroni, E. Pegoraro, G. P. Comi, S. D'Alfonso, L. H. van, F. Taroni, A. Al-Chalabi, J. Powell, V. Silani, t. S., Consortium S., Alessandro Filla

المساهمون: Fogh, I., Ratti, A., Gellera, C., Lin, K., Tiloca, C., Moskvina, V., Corrado, L., Sorarù, G., Cereda, C., Corti, S., Gentilini, D., Calini, D., Castellotti, B., Mazzini, L., Querin, G., Gagliardi, S., Bo, R. D., Conforti, F. L., Siciliano, G., Inghilleri, M., Saccà, Francesco, Bongioanni, P., Penco, S., Corbo, M., Sorbi, S., Filosto, M., Ferlini, A., Di, A. M., Signorini, S., Shatunov, A., Jones, A., Shaw, P. J., Morrison, K. E., Farmer, A. E., Damme, P. V., Robberecht, W., Chiò, A., Traynor, B. J., Sendtner, M., Melki, J., Meininger, V., Hardiman, O., Andersen, P. M., Leigh, N. P., Glass, J. D., Overste, D., Diekstra, F. P., Veldink, J. H., Van, M. A., Shaw, C. E., Weale, M. E., Lewis, C. M., Williams, J., Brown, R. H., Landers, J. E., Ticozzi, N., Ceroni, M., Pegoraro, E., Comi, G. P., D'Alfonso, S., Van, L. H., Taroni, F., Al-Chalabi, A., Powell, J., Silani, V., S., T., S., Consortium, Filla, Alessandro

مصطلحات موضوعية: Amyotrophic Lateral Sclerosi, Case-Control Studie, Chromosomes, Human, Pair 17, Prognosi, Genome-Wide Association Study

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000333269400022; volume:23; issue:8; firstpage:2220; lastpage:2231; numberofpages:12; journal:HUMAN MOLECULAR GENETICS; http://hdl.handle.net/11588/567190; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84897859556

الاتاحة: http://hdl.handle.net/11588/567190
https://doi.org/10.1093/hmg/ddt587

المؤلفون: P. T. van Doormaal, J. H. Weishaupt, K. Kenna, F. P. Diekstra, P. M. Andersen, A. M. Dekker, C. Tiloca, N. Marroquin, D. J. Overste, V. Pensato, P. Nürnberg, S. L. Pulit, R. D. Schellevis, D. Calini, J. Altmüller, L. C. Francioli, B. Muller, B. Castellotti, S. Motameny, J. Wolf, C. Gellera, A. C. Ludolph, L. H. van den Berg, C. Kubisch, J. E. Landers, J. H. Veldink, A. E. Volk, N. Ticozzi, F. Verde, A. Ratti, V. Silani

المساهمون: P.T. van Doormaal, N. Ticozzi, J.H. Weishaupt, K. Kenna, F.P. Diekstra, F. Verde, P.M. Andersen, A.M. Dekker, C. Tiloca, N. Marroquin, D.J. Overste, V. Pensato, P. Nürnberg, S.L. Pulit, R.D. Schellevi, D. Calini, J. Altmüller, L.C. Francioli, B. Muller, B. Castellotti, S. Motameny, A. Ratti, J. Wolf, C. Gellera, A.C. Ludolph, L.H. van den Berg, C. Kubisch, J.E. Lander, J.H. Veldink, V. Silani, A.E. Volk

مصطلحات موضوعية: ALS, amyotrophic lateral sclerosi, de novo mutation, disease pathway, motor neuron disease, trios, Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica, Settore BIO/18 - Genetica

Relation: info:eu-repo/semantics/altIdentifier/pmid/28714244; info:eu-repo/semantics/altIdentifier/wos/WOS:000412835700011; volume:38; issue:11; firstpage:1534; lastpage:1541; numberofpages:8; journal:HUMAN MUTATION; http://hdl.handle.net/2434/519726; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85026630875

الاتاحة: http://hdl.handle.net/2434/519726
https://doi.org/10.1002/humu.23295

المؤلفون: I. Fogh, K. Lin, J. Rooney, C. Gellera, F. P. Diekstra, A. Shatunov, M. A. van Es, P. Proitsi, A. Jones, W. Sproviero, A. Chiò, R. L. Mclaughlin, G. Sorarù, L. Corrado, D. Stahl, C. Cereda, B. Castellotti, J. D. Glass, S. Newhouse, R. Dobson, B. N. Smith, S. Topp, W. van Rheenen, V. Meininger, J. Melki, K. E. Morrison, P. J. Shaw, P. N. Leigh, P. M. Andersen, L. Mazzini, S. D'Alfonso, B. J. Traynor, P. Van Damme, W. Robberecht, R. H. Brown, J. E. Landers, O. Hardiman, C. M. Lewis, L. H. van den Berg, C. E. Shaw, J. H. Veldink, A. Al Chalabi, J. Powell, C. Tiloca, A. Ratti, R. Del Bo, G.P. Comi, N. Ticozzi, V. Silani

المساهمون: I. Fogh, K. Lin, C. Tiloca, J. Rooney, C. Gellera, F.P. Diekstra, A. Ratti, A. Shatunov, M.A. van E, P. Proitsi, A. Jone, W. Sproviero, A. Chiò, R.L. Mclaughlin, G. Sorarù, L. Corrado, D. Stahl, R. Del Bo, C. Cereda, B. Castellotti, J.D. Gla, S. Newhouse, R. Dobson, B.N. Smith, S. Topp, W. van Rheenen, V. Meininger, J. Melki, K.E. Morrison, P.J. Shaw, P.N. Leigh, P.M. Andersen, G.P. Comi, N. Ticozzi, L. Mazzini, S. D'Alfonso, B.J. Traynor, P. Van Damme, W. Robberecht, R.H. Brown, J.E. Lander, O. Hardiman, C.M. Lewi, L.H. van den Berg, C.E. Shaw, J.H. Veldink, V. Silani, A. Al Chalabi, J. Powell

مصطلحات موضوعية: genome-wide association, population-based cohort, motor-neuron disease, hexanucleotide repeat, al, C9ORF72, netaanalysi, expansion, diagnosi, criteria, Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica, Settore BIO/18 - Genetica

Relation: info:eu-repo/semantics/altIdentifier/pmid/27244217; info:eu-repo/semantics/altIdentifier/wos/WOS:000379420500013; volume:73; issue:7; firstpage:812; lastpage:820; numberofpages:9; journal:JAMA NEUROLOGY; http://hdl.handle.net/2434/394117; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84978101069

الاتاحة: http://hdl.handle.net/2434/394117
https://doi.org/10.1001/jamaneurol.2016.1114

المؤلفون: C. Gellera, V. Pensato, J. Agostini, C. Cereda, B. Castellotti, A. Bagarotti, A. Cagnin, C. Gabelli, L. Mazzini, G. Sorarù, S. D'Alfonso, C. Tiloca, R. Del Bo, L. Corrado, A. Ratti, S. Corti, P. Milani, G. Riboldi, F. Taroni, G.P. Comi, N. Ticozzi, V. Silani

المساهمون: C. Gellera, C. Tiloca, R. Del Bo, L. Corrado, V. Pensato, J. Agostini, C. Cereda, A. Ratti, B. Castellotti, S. Corti, A. Bagarotti, A. Cagnin, P. Milani, C. Gabelli, G. Riboldi, L. Mazzini, G. Sorarù, S. D'Alfonso, F. Taroni, G.P. Comi, N. Ticozzi, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia

Relation: Annual meeting of the American society of human genetics; http://hdl.handle.net/2434/265015

الاتاحة: http://hdl.handle.net/2434/265015

المؤلفون: R. Del Bo, S. Corti, N. Ticozzi, G.P. Comi, V. Silani, C. Tiloca, V. Pensato, L. Corrado, A. Ratti, B. Castellotti, B. Luciano, G. Sorarù, C. Cereda, L. Mazzini, C. Gellera

المساهمون: R. Del Bo, C. Tiloca, V. Pensato, L. Corrado, A. Ratti, S. Corti, B. Castellotti, B. Luciano, G. Sorarù, C. Cereda, L. Mazzini, N. Ticozzi, C. Gellera, G.P. Comi, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia

Relation: Annual Meeting of American Academy of Neurology; http://hdl.handle.net/2434/158037

الاتاحة: http://hdl.handle.net/2434/158037

المؤلفون: V. Pensato, C. Tiloca, L. Corrado, C. Bertolin, V. Sardone, R. DEL BO, D. Calini, J. Mandrioli, G. LAURIA PINTER, L. Mazzini, G. Querin, M. Ceroni, R. Cantello, S.P. Corti, B. Castellotti, G.M.E.A. Solda', S. Duga, G.P. Comi, C. Cereda, G. Sorarù, S. D'Alfonso, F. Taroni, C. E. Shaw, J. E. Landers, N. Ticozzi, A. Ratti, C. Gellera, V. Silani

المساهمون: V. Pensato, C. Tiloca, L. Corrado, C. Bertolin, V. Sardone, R. DEL BO, D. Calini, J. Mandrioli, G. LAURIA PINTER, L. Mazzini, G. Querin, M. Ceroni, R. Cantello, S.P. Corti, B. Castellotti, G.M.E.A. Solda', S. Duga, G.P. Comi, C. Cereda, G. Sorarù, S. D'Alfonso, F. Taroni, C.E. Shaw, J.E. Lander, N. Ticozzi, A. Ratti, C. Gellera, V. Silani

مصطلحات موضوعية: Neurology (clinical), Neurology, Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica

Relation: info:eu-repo/semantics/altIdentifier/pmid/25893256; info:eu-repo/semantics/altIdentifier/wos/WOS:000354950500036; volume:262; issue:5; firstpage:1376; lastpage:1378; numberofpages:3; journal:JOURNAL OF NEUROLOGY; http://hdl.handle.net/2434/272953; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84929834266

الاتاحة: http://hdl.handle.net/2434/272953
https://doi.org/10.1007/s00415-015-7739-y

المؤلفون: C. Colombrita, N. Ticozzi, A. Ratti, V. Silani, C. Gellera, B. Castellotti, C. Bragato, F. Taroni

المساهمون: C. Colombrita, C. Gellera, N. Ticozzi, A. Ratti, B. Castellotti, C. Bragato, F. Taroni, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia

Relation: ispartofbook:Programme and abstracts - 7th European ALS Congress - Research Workshop and Young Investigators Meeting; 7th European ALS Congress - Research Workshop and Young Investigators Meeting; firstpage:121; lastpage:122; http://hdl.handle.net/2434/71932

الاتاحة: http://hdl.handle.net/2434/71932

المؤلفون: C. Gellera, L. Corrado, B. Castellotti, M. Plumari, Y. Carlomagno, C. Bragato, L. Mazzini, F. Taroni, N. Ticozzi, A. Ratti, C. Colombrita, V. Silani

المساهمون: C. Gellera, N. Ticozzi, A. Ratti, L. Corrado, B. Castellotti, C. Colombrita, M. Plumari, Y. Carlomagno, C. Bragato, L. Mazzini, F. Taroni, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia

Relation: ispartofbook:Atti; IV Meeting on the Molecular Mechanisms of Neurodegeneration; firstpage:P01; lastpage:P01; http://hdl.handle.net/2434/71712

الاتاحة: http://hdl.handle.net/2434/71712

المؤلفون: C. Gellera, M. Plumari, B. Castellotti, G. Luaria, C. Fallini, D. Testa, M. Corbo, F. Taroni, N. Ticozzi, PASSARIELLO, PAOLA, A. Ratti, C. Colombrita, V. Silani

المساهمون: C. Gellera, N. Ticozzi, P. Passariello, A. Ratti, M. Plumari, C. Colombrita, B. Castellotti, G. Luaria, C. Fallini, D. Testa, M. Corbo, F. Taroni, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia

Relation: ispartofbook:Atti congressuali; Mutant SOD1 and familial ALS: from the molecule to man; firstpage:86; lastpage:86; http://hdl.handle.net/2434/42990

الاتاحة: http://hdl.handle.net/2434/42990

المؤلفون: C. Colombrita, N. Ticozzi, A Ratti, V. Silani, C. Gellera, B. Castellotti, C. Bragato, F. Taroni

المساهمون: C. Colombrita, C. Gellera, N. Ticozzi, B. Castellotti, A. Ratti, C. Bragato, F. Taroni, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia

Relation: ispartofbook:Abstract book; 5th European ALS Congress - Research Workshop and Young Investigators Meeting; firstpage:17; lastpage:17; http://hdl.handle.net/2434/42991

الاتاحة: http://hdl.handle.net/2434/42991

المؤلفون: B. N. Smith, N. Ticozzi, C. Fallini, A. S. Gkazi, S. Topp, K. P. Kenna, E. L. Scotter, J. Kost, P. Keagle, J. W. Miller, D. Calini, C. Vance, E. W. Danielson, C. Troakes, C. Tiloca, S. Al Sarraj, E. A. Lewis, A. King, C. Colombrita, V. Pensato, B. Castellotti, J. de Belleroche, F. Baas, A. LMA ten Asbroek, P. C. Sapp, D. McKenna Yasek, R. L. McLaughlin, M. Polak, S. Asress, J. Esteban Pérez, J. L. Muñoz Blanco, M. Simpson, S. D’Alfonso, L. Mazzini, G.P. Comi, R. Del Bo, M. Ceroni, S. Gagliardi, G. Querin, C. Bertolin, W. van Rheenen, F. P. Diekstra, G. Lauria, S. Duga, S. Corti, C. Cereda, L. Corrado, G. Sorarù, K. E. Morrison, K. L. Williams, G. A. Nicholson, I. P. Blair, P. A. Dion, C. S. Leblond, G. A. Rouleau, O. Hardiman, J. H. Veldink, L. H. van den Berg, A. Al Chalabi, H. Pall, P. J. Shaw, M. R. Turner, K. Talbot, F. Taroni, A. García Redondo, Z. Wu, J. D. Glass, C. Gellera, A. Ratti, R. H. Brown, V. Silani, C. E. Shaw, J. E. Landers

المساهمون: B.N. Smith, N. Ticozzi, C. Fallini, A.S. Gkazi, S. Topp, K.P. Kenna, E.L. Scotter, J. Kost, P. Keagle, J.W. Miller, D. Calini, C. Vance, E.W. Danielson, C. Troake, C. Tiloca, S. Al Sarraj, E.A. Lewi, A. King, C. Colombrita, V. Pensato, B. Castellotti, J. de Belleroche, F. Baa, A. LMA ten Asbroek, P.C. Sapp, D. McKenna Yasek, R.L. Mclaughlin, M. Polak, S. Asre, J. Esteban Pérez, J.L. Muñoz Blanco, M. Simpson, S. D’Alfonso, L. Mazzini, G.P. Comi, R. Del Bo, M. Ceroni, S. Gagliardi, G. Querin, C. Bertolin, W. van Rheenen, F.P. Diekstra, G. Lauria, S. Duga, S. Corti, C. Cereda, L. Corrado, G. Sorarù, K.E. Morrison, K.L. William, G.A. Nicholson, I.P. Blair, P.A. Dion, C.S. Leblond, G.A. Rouleau, O. Hardiman, J.H. Veldink, L.H. van den Berg, A. Al Chalabi, H. Pall, P.J. Shaw, M.R. Turner, K. Talbot, F. Taroni, A. García Redondo, Z. Wu, J.D. Gla, C. Gellera, A. Ratti, R.H. Brown, V. Silani, C.E. Shaw, J.E. Landers

مصطلحات موضوعية: Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica, Settore BIO/18 - Genetica, Settore MED/03 - Genetica Medica

Relation: info:eu-repo/semantics/altIdentifier/pmid/25374358; info:eu-repo/semantics/altIdentifier/wos/WOS:000344167900011; volume:84; issue:2; firstpage:324; lastpage:331; numberofpages:8; journal:NEURON; http://hdl.handle.net/2434/243427; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84908224269

الاتاحة: http://hdl.handle.net/2434/243427
https://doi.org/10.1016/j.neuron.2014.09.027

المؤلفون: C. Gellera, C. Tiloca, L. Corrado, V. Pensato, J. Agostini, C. Cereda, B. Castellotti, A. Bagarotti, A. Cagnin, P. Milani, C. Gabelli, L. Mazzini, G. Sorarù, S. D'Alfonso, F. Taroni, R. Del Bò, A. Ratti, S. Corti, G. Riboldi, G.P. Comi, N. Ticozzi, V. Silani

المساهمون: C. Gellera, C. Tiloca, R. Del Bò, L. Corrado, V. Pensato, J. Agostini, C. Cereda, A. Ratti, B. Castellotti, S. Corti, A. Bagarotti, A. Cagnin, P. Milani, C. Gabelli, G. Riboldi, L. Mazzini, G. Sorarù, S. D'Alfonso, F. Taroni, G.P. Comi, N. Ticozzi, V. Silani

مصطلحات موضوعية: Settore MED/26 - Neurologia, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica

Relation: info:eu-repo/semantics/altIdentifier/pmid/23138764; info:eu-repo/semantics/altIdentifier/wos/WOS:000313554700013; volume:84; issue:2; firstpage:183; lastpage:187; numberofpages:5; journal:JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY; http://hdl.handle.net/2434/211353; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84872676800

الاتاحة: http://hdl.handle.net/2434/211353
https://doi.org/10.1136/jnnp-2012-303433

المؤلفون: C. Gellera, N. Ticozzi, V. Pensato, L. Nanetti, A. Castucci, B. Castellotti, G. Lauria, F. Taroni, V. Silani, C. Mariotti

المساهمون: C. Gellera, N. Ticozzi, V. Pensato, L. Nanetti, A. Castucci, B. Castellotti, G. Lauria, F. Taroni, V. Silani, C. Mariotti

مصطلحات موضوعية: Spinocerebellar ataxia type 2, Ataxin 2, ATXN2, Amyotrophic lateral sclerosi, Neurodegenerative disorder, Triplet repeat, CAG, Polyglutamine disorders, Settore MED/26 - Neurologia, Settore BIO/18 - Genetica

Relation: info:eu-repo/semantics/altIdentifier/pmid/22425256; info:eu-repo/semantics/altIdentifier/wos/WOS:000306070800050; volume:33; issue:8; firstpage:e.15; lastpage:e.21; numberofpages:7; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2434/210174; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84861888532

الاتاحة: http://hdl.handle.net/2434/210174
https://doi.org/10.1016/j.neurobiolaging.2012.02.004

المؤلفون: C. Tiloca, V. Pensato, A. Castucci, G. Sorarù, R. Del Bo, L. Corrado, C. Cereda, C. D'Ascenzo, L. Mazzini, B. Castellotti, C. Gellera, A. Ratti, G.P. Comi, N. Ticozzi, V. Silani

المساهمون: C. Tiloca, A. Ratti, V. Pensato, A. Castucci, G. Sorarù, R. Del Bo, L. Corrado, C. Cereda, C. D'Ascenzo, G.P. Comi, L. Mazzini, B. Castellotti, N. Ticozzi, C. Gellera, V. Silani

مصطلحات موضوعية: ALS (Amyotrophic lateral sclerosis), VCP (valosin-containing protein), Genetics, Settore MED/26 - Neurologia, Settore BIO/18 - Genetica

Relation: info:eu-repo/semantics/altIdentifier/pmid/22137929; info:eu-repo/semantics/altIdentifier/wos/WOS:000180450900015; volume:33; issue:3; firstpage:630.e1; lastpage:630.e2; numberofpages:2; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2434/174322; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84855809916

الاتاحة: http://hdl.handle.net/2434/174322
https://doi.org/10.1016/j.neurobiolaging.2011.10.025

المؤلفون: A. Ratti, R. Del Bo, C. Tiloca, M. Ranieri, S.P. Corti, N. Ticozzi, G.P. Comi, V. Silani, L. Corrado, B. Castellotti, I. Fogh, C. Cereda, C. D'Ascenzo, A. Bagarotti, V. Pensato, S. Gagliardi, D. Calini, L. Mazzini, F. Taroni, M. Ceroni, G. D. Oggioni, K. Lin, J. F. Powell, G. Sorarù, S. D'Alfonso, C. Gellera

المساهمون: A. Ratti, L. Corrado, B. Castellotti, R. Del Bo, I. Fogh, C. Cereda, C. Tiloca, C. D'Ascenzo, A. Bagarotti, V. Pensato, M. Ranieri, S. Gagliardi, D. Calini, L. Mazzini, F. Taroni, S.P. Corti, M. Ceroni, G.D. Oggioni, K. Lin, J.F. Powell, G. Sorarù, N. Ticozzi, G.P. Comi, S. D'Alfonso, C. Gellera, V. Silani

مصطلحات موضوعية: Amyotrophic lateral sclerosi, C9ORF72, Frontotemporal dementia, Haplotype analysi, Mutation analysi, Repeat expansion, Settore MED/26 - Neurologia, Settore MED/03 - Genetica Medica, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica, Settore BIO/18 - Genetica

Relation: info:eu-repo/semantics/altIdentifier/pmid/22766072; info:eu-repo/semantics/altIdentifier/wos/WOS:000308088500031; volume:33; issue:10; firstpage:2528.e7; lastpage:2528.e14; numberofpages:8; journal:NEUROBIOLOGY OF AGING; http://hdl.handle.net/2434/207113; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84864392867

الاتاحة: http://hdl.handle.net/2434/207113
https://doi.org/10.1016/j.neurobiolaging.2012.06.008