المؤلفون: Graf T., Martinez A. A., Bello G., Dellicour S., Lemey P., Colizza V., Mazzoli M., Poletto C., Cardoso V. L. O., da Silva A. F., Baumeister E., Campos J., Pontoriero A., Martin I., Ferguson K., Johnson D., Beckles S., Forde K., Sosa A., Melendez R., Loayza R., Avila C., Fernandez E. E. F., Otazo C. J. G., Siqueira M. M., Motta F. C., de Oliveira Santos K. C., Abbud A., dos Santos M. C., de Almeida Ferreira J., Fasce R., Fernandes J., Rangel S. G., Mercado M. M., Pelaez D., Soto-Garita C., Cordero-Laurent E., Duarte-Martinez F., Brenes H., Sanchez I. M., Imbert Y., Caicedo A. B., de Mora Coloma D. J., Lopez D. X. S., Alvarado D. G. J., Moran D. L. M., Pacheco C., Mendoza L., Whyte-Chin J., Abdul-Kadir M., Boncy J., Journel I., Paz M. C., Alvarado S. C., Avilez S., Brown M., Arambula C. E. W., Gonzalez E. R., Gonzalez C. M., Moreno Arevalo B., Franco D., Lopez-Verges S., Pascale J. M., Vazquez C., Gonzalez S., Serrano N. R., Rojas C. P. P., Pinas P., Asebeh N., Carrington C. V. F., Sahadeo N. S. D., Chiparelli H., Goni N., Rodriguez L., D'Angelo P., Resende P. C., Franco L., Gresh L., Gabastou J. -M., Rodriguez A., Vicari A., Aldighieri S., Mendez-Rico J., Leite J. A.

المساهمون: Graf, T., Martinez, A. A., Bello, G., Dellicour, S., Lemey, P., Colizza, V., Mazzoli, M., Poletto, C., Cardoso, V. L. O., da Silva, A. F., Baumeister, E., Campos, J., Pontoriero, A., Martin, I., Ferguson, K., Johnson, D., Beckles, S., Forde, K., Sosa, A., Melendez, R., Loayza, R., Avila, C., Fernandez, E. E. F., Otazo, C. J. G., Siqueira, M. M., Motta, F. C., de Oliveira Santos, K. C., Abbud, A., dos Santos, M. C., de Almeida Ferreira, J., Fasce, R., Fernandes, J., Rangel, S. G., Mercado, M. M., Pelaez, D., Soto-Garita, C., Cordero-Laurent, E., Duarte-Martinez, F., Brenes, H., Sanchez, I. M., Imbert, Y., Caicedo, A. B., de Mora Coloma, D. J., Lopez, D. X. S., Alvarado, D. G. J., Moran, D. L. M., Pacheco, C., Mendoza, L., Whyte-Chin, J., Abdul-Kadir, M., Boncy, J., Journel, I., Paz, M. C., Alvarado, S. C., Avilez, S., Brown, M., Arambula, C. E. W., Gonzalez, E. R., Gonzalez, C. M., Moreno Arevalo, B., Franco, D., Lopez-Verges, S., Pascale, J. M., Vazquez, C., Gonzalez, S., Serrano, N. R., Rojas, C. P. P., Pinas, P., Asebeh, N., Carrington, C. V. F., Sahadeo, N. S. D., Chiparelli, H., Goni, N., Rodriguez, L., D'Angelo, P., Resende, P. C., Franco, L., Gresh, L., Gabastou, J. -M., Rodriguez, A., Vicari, A., Aldighieri, S., Mendez-Rico, J., Leite, J. A.

Relation: info:eu-repo/semantics/altIdentifier/pmid/38418815; info:eu-repo/semantics/altIdentifier/wos/WOS:001178091600043; volume:15; issue:1; journal:NATURE COMMUNICATIONS; https://hdl.handle.net/11577/3527301

الاتاحة: https://hdl.handle.net/11577/3527301
https://doi.org/10.1038/s41467-024-46143-9

المؤلفون: Galassi G., Mazzoli M., Ariatti A., Bedin R., Marzullo D., Bastia E., Agnoletto V., Gozzi M., Valzania F., Meletti S., Marchioni A.

المساهمون: Galassi, G., Mazzoli, M., Ariatti, A., Bedin, R., Marzullo, D., Bastia, E., Agnoletto, V., Gozzi, M., Valzania, F., Meletti, S., Marchioni, A.

مصطلحات موضوعية: Guillain−Barré syndrome, internal calibration, mechanical ventilation, respiratory failure, tracheostomy

Relation: info:eu-repo/semantics/altIdentifier/pmid/37823704; info:eu-repo/semantics/altIdentifier/wos/WOS:001083174200001; volume:31; issue:1; firstpage:N/A; lastpage:N/A; journal:EUROPEAN JOURNAL OF NEUROLOGY; https://hdl.handle.net/11380/1335772; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85173813537

الاتاحة: https://hdl.handle.net/11380/1335772
https://doi.org/10.1111/ene.16090

المؤلفون: Gutierrez, B, Tsui, JL-, Pullano, G, Mazzoli, M, Gangavarapu, K, Inward, RPD, Bajaj, S, Evans Pena, R, Busch-Moreno, S, Suchard, MA, Pybus, OG, Dunner, A, Puentes, R, Ayala, S, Fernandez, J, Araos, R, Ferres, L, Colizza, V, Kraemer, MUG

Relation: https://doi.org/10.1093/pnasnexus/pgae483

الاتاحة: https://doi.org/10.1093/pnasnexus/pgae483
https://ora.ox.ac.uk/objects/uuid:95acb0fa-031d-4dad-8898-5ffbc5bf19b9

المؤلفون: Beauverd, M., Mazzoli, M., Pralong, J., Tomczyk, M., Eychmüller, S., Gaertner, J.

المصدر: Swiss medical weekly, vol. 154, pp. 3590

مصطلحات موضوعية: Humans, Palliative Care/methods, Uncertainty, Health Personnel, Communication, Physicians, Deep Sedation/methods, Terminal Care/methods, Hypnotics and Sedatives/therapeutic use

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38579308; info:eu-repo/semantics/altIdentifier/eissn/1424-3997; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_DFF0DD67B0366; https://serval.unil.ch/notice/serval:BIB_DFF0DD67B036; https://serval.unil.ch/resource/serval:BIB_DFF0DD67B036.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_DFF0DD67B036
https://doi.org/10.57187/s.3590
https://serval.unil.ch/resource/serval:BIB_DFF0DD67B036.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_DFF0DD67B0366

المؤلفون: Natali P., Debbia D., Troiano T., Napodano C., Spinella A., Amati G., Filippini D., Zani R., Alfano G., Colaci E., Maccaferri M., Galassi G., Mazzoli M., Ariatti A., Basile U., Mascia M. T., Palladini G., Giuggioli D., Sandri G.

المساهمون: Natali, P., Debbia, D., Troiano, T., Napodano, C., Spinella, A., Amati, G., Filippini, D., Zani, R., Alfano, G., Colaci, E., Maccaferri, M., Galassi, G., Mazzoli, M., Ariatti, A., Basile, U., Mascia, M. T., Palladini, G., Giuggioli, D., Sandri, G.

Relation: volume:47; issue:3; firstpage:277; lastpage:284; journal:BIOCHIMICA CLINICA; https://hdl.handle.net/11380/1340294; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85174193816

الاتاحة: https://hdl.handle.net/11380/1340294
https://doi.org/10.19186/BC_2023.040

المؤلفون: Aguilar, J, Bassolas, A, Ghoshal, G, Hazarie, S, Kirkley, A, Mazzoli, M, Meloni, S, Mimar, S, Nicosia, V, Ramasco, JJ, Sadilek, A

Relation: SCIENTIFIC REPORTS; ARTN 3816; https://qmro.qmul.ac.uk/xmlui/handle/123456789/77585

الاتاحة: https://qmro.qmul.ac.uk/xmlui/handle/123456789/77585
https://doi.org/10.1038/s41598-022-06720-8

المؤلفون: Giovannini G., Turchi G., Mazzoli M., Vaudano A. E., Meletti S.

المساهمون: Giovannini, G., Turchi, G., Mazzoli, M., Vaudano, A. E., Meletti, S.

مصطلحات موضوعية: Generalized genetic epilepsy, Influenza associated encephalopathy (IAE), Influenza B, New onset status epilepticus

Relation: info:eu-repo/semantics/altIdentifier/pmid/33598653; info:eu-repo/semantics/altIdentifier/wos/WOS:000704806000009; volume:16; firstpage:100413; lastpage:100413; numberofpages:1; journal:EPILEPSY & BEHAVIOR REPORTS; http://hdl.handle.net/11380/1236896; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85100402458

الاتاحة: http://hdl.handle.net/11380/1236896
https://doi.org/10.1016/j.ebr.2020.100413

المؤلفون: MAZZOLI, M., RICCI, A., VAUDANO, A. E., MARCACCI, M., MARCHINI, S., BERGONZINI, P., DI PIERRO, E., PISCHIK, E., IUGHETTI, L., PIETRANGELO, A., MELETTI, S., VENTURA, P.

المصدر: European Review for Medical & Pharmacological Sciences; Apr2024, Vol. 28 Issue 8, p3268-3274, 7p

المؤلفون: Pansanel, J., Legoll, V., López García, A., Kissa, P., Heredia, A., Henschel, R., Tran, V., Astalos, J., Rosemond Dora, J., Habala, O., Obregón, M., Sáinz-Pardo Díaz, J., Ramasco, J.J., Tugores, A., Artigues, M., Mazzoli, M.

Relation: https://zenodo.org/communities/siesta; https://doi.org/10.5281/zenodo.11485213; https://doi.org/10.5281/zenodo.11485214; oai:zenodo.org:11485214

الاتاحة: https://doi.org/10.5281/zenodo.11485214

المؤلفون: Sandri, G., Spinella, A., Natali, P., Debbia, D., Campioli, D., Bari, A., Amati, G., Galassi, G., Mazzoli, M., Alfano, G., Fontana, F., Trenti, T., Mascia, M.T.

المصدر: Annals of the Rheumatic Diseases ; volume 79, page 1559-1560 ; ISSN 0003-4967

الاتاحة: https://doi.org/10.1136/annrheumdis-2020-eular.5360
https://api.elsevier.com/content/article/PII:S0003496724694367?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0003496724694367?httpAccept=text/plain
https://syndication.highwire.org/content/doi/10.1136/annrheumdis-2020-eular.5360

المؤلفون: Coniglio S., Turchi G., Giovannini G., Mazzoli M., Meletti S., Vaudano A. E.

المساهمون: Coniglio, S., Turchi, G., Giovannini, G., Mazzoli, M., Meletti, S., Vaudano, A. E.

مصطلحات موضوعية: Anti-SOX1-antibodie, Case report, Guillain-Barré syndrome, Paraneoplastic syndrome, Autoantibodie, Human, SOXB1 Transcription Factor, Guillain-Barre Syndrome, Lung Neoplasm, Peripheral Nervous System Diseases

Relation: info:eu-repo/semantics/altIdentifier/pmid/35391602; info:eu-repo/semantics/altIdentifier/wos/WOS:000779627100003; volume:43; issue:6; firstpage:3979; lastpage:3982; journal:NEUROLOGICAL SCIENCES; https://hdl.handle.net/11380/1277905; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85127640713

الاتاحة: https://hdl.handle.net/11380/1277905
https://doi.org/10.1007/s10072-022-06055-2

المؤلفون: Mazzoli, M., Sánchez, Angel

المساهمون: European Commission, Ministerio de Economía y Competitividad (España)

مصطلحات موضوعية: Agents, Agent, Coordination, Proportional imitation, Best response, Network, Scale free, Matemáticas

Relation: info:eu-repo/grantAgreement/EC/H2020/640772; info:eu-repo/grantAgreement/EC/H2020/662725; Gobierno de España. FIS2015-64349-P; Mazzoli, M. y Sánchez A. (2017). Equilibria, information and frustration in heterogeneous network games with conflicting preferences. Journal of Statistical Mechanics: Theory and Experiment,2017.; http://hdl.handle.net/10016/29179; https://doi.org/10.1088/1742-5468/aa9347; Journal of Statistical Mechanics: Theory and Experiment; 2017; AR/0000020825

الاتاحة: http://hdl.handle.net/10016/29179
https://doi.org/10.1088/1742-5468/aa9347

المؤلفون: Mazzoli M., Lombardini S.

المساهمون: Mazzoli, M., Lombardini, S.

مصطلحات موضوعية: Business fluctuation, Industrial organization and macroeconomics

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000692829300005; volume:69 (2021) 103335; firstpage:1; lastpage:16; numberofpages:16; journal:JOURNAL OF MACROECONOMICS; https://hdl.handle.net/11567/1083004; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85107691380

الاتاحة: https://hdl.handle.net/11567/1083004
https://doi.org/10.1016/j.jmacro.2021.103335

المؤلفون: Astrea, G., Battini, R., Berardinelli, A., Bertini, E., Bruno, C., Catteruccia, M., Comi, G.P., D’Amico, A., Fattori, F., Fiorillo, C., Magri, F., Mercuri, E., Messina, S., Mongini, T., Mora, M., Morani, F., Moro, F., Pane, M., Pegoraro, E., Pini, A., Politano, L., Ricci, F., Sframeli, M., Toscano, A., Santorelli, F.M., Lenzi, S., Bello, L., Corti, S., Donati, M.A., Tubili, F., Morrone, A., la Marca, G., Daniotti, M., Evoli, A., Ferlini, A., Garibaldi, M., Rendu, J., Brocard, J., Lacene, E., Fauré, J., Brochier, G., Beuvin, M., Labasse, C., Madelaine, A., Malfatti, E., Bevilacqua, J.A., Lubieniecki, F., Monges, S., Taratuto, A.L., Laporte, J., Marty, I., Antonini, G., Romero, N.B., M.L.*, Lombardo, Maggi, L., Mirabella, M., Musumeci, O., Paoletti, M., Pichiecchio, A., Pennisi, E.M., Ricci, G., Rodolico, C., Marchese, M., Siciliano, G., Tasca, G., Mele, F., Ruggiero, L., Vercelli, L., Bettio, C., Tripodi, S., Govi, M., Bucci, E., Di Muzio, A., Scarlato, M., Villa, L., D’Angelo, G., Filosto, M., Piras, R., Maioli, M.A., Massa, R., Previtali, S., Angelini, C., Moggio, M., Santoro, L., Tomelleri, G., Tupler, R., Udd, B., Sera, F., Maranda, L., Vianello, A., Vissing, J., Zeviani, M., Barp, A., Laforet, P., Monforte, M., Ricci, E., Choumert, A., Stojkovic, T., Semplicini, C., Stramare, R., Scheidegger, O., Haberlova, J., Straub, V., Marini Bettolo, C., Løkken, N., Diaz-Manera, J., Urtizberea, J.A., Kynčl, M., Walter, M.C., Carlier, R.Y., Zambon, A.A., Albamonte, E., Baranello, G., Gandossini, S., Gualandi, F., Natali Sora, M.G., Politano, A., Sansone, V., Vita, G.L., Previtali, S.C., Villa, M., Fusto, A., Vianello, S., Merlo, B., Pedemonte, M., Tacchetti, P., Lanzillotta, V., Trucco, F., De Mattia, E., Rao, F., Calore, C., Hoffman, E.P., Morgenroth, L., Gordish-Dressman, H., McDonald, C.M., Costa, R., Rodia, M.T., Santi, S., Lattanzi, G., Papa, V., Pegoraro, V., Cenacchi, G., M, Sframeli, Ciranni, A., Versaci, A., Di Bella, V., Ferlazzo, V., Gitto, E., Aguennouz, M., Vita, G., Mendell, J.R., Al-Zaidy, S., Lehman, K.J., McColly, M., Lowes, L.P., Alfano, L.N., Miller, N.F., Iammarino, M.A., Church, K., Bernat Fuertes, M., Ogrinc, F.G., L’Italien, J., Kernbauer, E., Shah, S., Sproule, D.M., Feltner, D.E., Day, J.W., Chiriboga, C.A., Crawford, T.O., Darras, B.T., Finkel, R.S., Connolly, A.M., Iannaccone, S.T., Kuntz, N.L., Peña, L.D.M., Schultz, M., Shieh, P.B., Smith, E.C., Shah, A., Ouyang, H., Macek, T.A., Muehring, L.M., Kaspar, B.K., Masson, R., Servais, L., Deconinck, N., Klein, A., Darras, B., Kletzl, H., Cleary, H., El-Khairi, M., Seabrook, T., Czech, C., Gerber, M., Nguyen, C., Gelblin, K., Gorni, K., Rossi, R., Falzarano, M.F., Margutti, A., Spedicato, N., El Dani, R., Fabris, M., Neri, M., Fini, S., Rimessi, P., Johansson, C., Al-Khalili Szigyarto, C., Savarese, M., Johari, M., Jonson, P.H., Koivunen, S., Quareshi, T., Vihola, A., Hackman, P., Gemelli, C., Trevisan, L., Fabbri, S., Pisciotta, L., Meo, G., Traverso, M., Zara, F., Minetti, C., Schenone, A., Mandich, P., Grandis, M., C, Dosi, Cassandrini, D., Rubegni, A., Tolomeo, D., Giannini, F., Malandrini, A., Tonin, P., Volpi, N., Potter, R.A., Griffin, D.A., Heller, K.N., Rodino-Klapac, L.R., Salsi, V., Salani, M., Kaufman, P.D., Green, M.R., Vallarola, A., Termanini, A., Cortini, M., Ghiaroni, V., Forcato, M., Germinario, E., D’Antona, G., Blaauw, B., Genazzani, A.A., Filigheddu, N., Santoro, M., Cotti Piccinelli, S., Lamperti, C., Servidei, S., Santorelli, F.A., Simoncini, C., Primiano, G., Galvagni, A., Caria, F., Gallo Cassarino, S., Baldelli, E., Necchini, N., Carelli, V., Padovani, A., Mancuso, M., Verardo, M., Lupica, A., Ripolone, M., Vattemi, G., Sciacco, M., Nigro, V., Lucchini, M., De Arcangelis, V., De Fino, C., Santovito, L., Brigati, G., Diana, C., Panicucci, C., Broda, P., Nesti, C., Santorelli, F., Baronchelli, C., G, Greco, Frezza, E., Rastelli, E., Terracciano, C., Merlonghi, G., Pugliese, S., Tartaglione, T., Calabrò, F., Petrucci, A., M, Catteruccia, Colia, G., Bonetti, A.M., Carlesi, A., Bruno, G.M., Di Matteo, S., Valentino, M.C., Oselin, M., Martinotti, C., Xoxi, E., Colombo, G.L., Russo, A., LoMauro, A., Velardo, D., Turconi, A.C., Bresolin, N., Aliverti, A., D’Angelo, M.G., Ferrero, A., Rossi, M., Palermo, C., Giannotta, M., Rolle, E., Derchi, M., Gardani, A., Balottin, U., Giugliano, T., Torella, A., Garofalo, A., Onore, M.E., Del Vecchio Blanco, F., Piluso, G., Selvatici, R., Trabanelli, C., Buldrini, B., Venturoli, A., Fortunato, F., Potulska, A., Emandi, A.C., Lehman, I., Herczegfalvi, A., Guergueltcheva, V., Kyriakides, T., Sifi, Y., Molnar, M.J., Burnyte, B., Shatillo, A., Vlodavets, D., F.1, Gualandi, Scali, M., Ciscato, P., Menni, F., Mani, E., Falzarano, M.S., Baratto, S., Nesich, V., Iacomino, M., Castiglione, V., Giannoni, A., Florio, F., Rocchi, A., Emdin, M., Fratazzi, C., Naughton, E., Krenz, H., Distefano, M.G., Madia, F., Mauri, E., Ronchi, D., Govoni, A., Brusa, R., Zangaro, V., Lazzarotto, A., Fanin, M., Picillo, E., Ergoli, M., Principi, E., Del Zotto, G., Antonini, F., Ognio, M., Bruzzone, S., Gazzerro, E., Raffaghello, L., Lai, E., Torri, F., Chico, L., Fuccillo, E., Nucera, G., Greco, G., Di Mauro, R., Di Girolamo, S., Siliquini, S., Meneri, M., Cinnante, C., Triulzi, F., Vergari, M., Cogiamanian, F., Stocchetti, N., Calderini, E., Sansone, V.A., Corti, S.P., Pera, M.C., Kirschner, J., Goemans, N., Tichy, M., Yeung, W.Y., Annoussamy, M., Cleary, Y., Carraro, E., Salmin, F., Lunetta, C., Comi, G., Sconfienza, L.M., Manenti, G.F., Valeria, V., Morettini, V., Gagliano, N., Bonanno, S., Marcuzzo, S., Malacarne, C., Giagnorio, E., Zanin, R., Andreetta, F., Simoncini, O., Bernasconi, P., Mantegazza, R., Cherchi, C., Chiarini Testa, M.B., Bonetti, A., Rollo, M., Bianchi, R., Longo, A., Nicita, F., Corsetti, T., Cutrera, R., Bruno, G., Allegorico, L., Lombardi, L., Napolitano, F., Sampaolo, S., Bertocci, G., Guglielmi, V., Matà, S., Federico, A., Merlini, L., Matucci-Cerinic, C., Fionda, L., Vanoli, V., Leonardi, L., Loreti, S., Morino, S., Micaloni, A., Raffa, S., Blasio, G., Varone, A., Marrosu, G., Moroni, I., Fusco, C., Sabatelli, P., Morandi, L., Grilli, A., Bicciato, S., Palmio, J., Poza, J.J., Weinberg, J., Olive, M., Cobo, A.M., Sarparanta, J., García-Bragado, F., Gibertini, S., Saredi, S., Matalonga, L., Farina, L., Ardissone, A., Caumo, L., Bozzoni, V., Cester, G., Gabrieli, J., Causin, F., Sorarù, G., Galatolo, D., D’Amore, F., Doccini, S., Giglio, S., Pantaleo, M., Guarducci, S., Telese, R., De Rosa, A., Napoli, L., Fagiolari, G., Montomoli, M., Mancardi, M.M., Mari, F., Morana, G., Guerrini, R., Arceri, S., Ravaglia, S., Cosentino, G., Alfonsi, E., Pugliese, A., Volta, S., Oteri, R., Della Marca, G., Brunetti, V., Sancricca, C., Vollono, C., Macone, A., Missaglia, S., Noguera, N.I., Palma, E., Tavian, D., Pennisi, E.M.M., Tavilla, G., DiSfetano, M.G., Di Iorio, G., Melone, M.A.B., Esposito, T., Tartara, A., Cena, H., Stefan, C., Brondani, G., Trevisi, E., Martinuzzi, A., Brizzi, T., Peverelli, L., Legati, A., Lamantea, E., Nasca, A., Marchet, S., Lerario, A., Galimberti, V., Ghezzi, D., Vitale, R., Antonio Toscano, A., Sacchini, M., D’Angelo, R., Boschetti, E., Caporali, L., Lodi, R., Pironi, L., De Giorgio, R., Rinaldi, R., Fernandez-Vizarra, E., Tiranti, V., Pinzan, E., Marozzo, R., Montano, V., Calì Cassi, L., Botta, A., Silvestri, G., Cintoni, M., Pulcini, G., Palombi, C., Salvia, M., Tammam, G., De Lorenzo, A., Carlesi, D., Diodato, D., Bonanno, C., Nicocia, G., Foti, F.M., Ricciardi, R., Bocci, T., Maestri, M., Guida, M., Bonuccelli, U., Vanoli, F., Di Pasquale, A., Vizzaccaro, E., Sinicropi, S., Pancheri, E., Sajeva, G., Goffi, F., Zanoni, M., Bertolasi, L., Abati, E., Girolamo, F., Lia, A., Giannini, M., Fornaro, M., Amati, A., D’Abbicco, D., Tampoia, M., Serlenga, L., Iannone, F., Trojano, M., Frigeri, A., Ticci, C, Battisti, C., Melani, F., Alì, G., Sartucci, F., Ceppa, I., Dosi, C., Baldacci, J., Dati, E., Frosini, S., Conte, R., Calderisi, M., Sansone, F., Diodato, G., Pala, A.P., Scudellari, M.C., Tonacci, A., Ceppa, C., Giorgolo, F., Marfisi, D., Del Bo, R., Faravelli, I., Gagliardi, D., Costamagna, G., Torrente, Y., Malcontenti, S., Coluccini, M., Perazza, S., Amador, C., Grande, A., Roccella, S., Spezzaneve, A., Fantacci, M.E., Iori, E., Ariatti, A., Mazzoli, M., Fini, N., Genovese, M., Galassi, G., Sette, E., Tugnoli, V., Rispoli, M.G., Mero, S., Vitale, M., Barbone, F., Di Stefano, V., De Angelis, M.V., Ruggieri, A., Cauley, E.S., Spivey, T., Manzini, M.C., Orlandi, R., Gajofatto, A.

المصدر: Acta Myologica

مصطلحات موضوعية: musculoskeletal diseases, nonsense variants, ABSTRACTS OF POSTER COMMUNICATIONS (listed in order of presentation), P 1-2 SMA, Congenital myopathies and CMD, MUSCLE CLUB SESSION (in alphabetical order of the first Author), ABSTRACTS OF ORAL COMMUNICATIONS (in alphabetical order of the first Author), ABSTRACTS OF INVITED LECTURES (in alphabetical order of the first Author), P. 2-1 Mitochondrial and metabolic myopathies, Duchenne/Becker muscular dystrophy, Proceedings of the Xix Congress of the Italian Society of Myology, P. 2-2. Myotonias, Channellopathies, Neuromuscular Junction Disorders and inflammatory myopathies, P. 2-3 Miscellanea, Session 1. 6 giugno dalle ore 14.30-15.30, NGS, DMD, congenital myopathy, P 1-1 Muscular dystrophies, Sessione 2 7 giugno dalle ore 14.30-15.30, hypotonia

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::0a1599d89e0cd061ff2824e8b2eaabff
http://europepmc.org/articles/PMC6598409

المؤلفون: Mazzoli M, Morini M., Terna P.

المساهمون: Mazzoli, M, Morini, M., Terna, P.

مصطلحات موضوعية: Macroeconomic, Industrial Organization and Macroeconomic, Business fluctuations

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/isbn/9781108482608; info:eu-repo/semantics/altIdentifier/wos/WOS:000649544000010; firstpage:1; lastpage:230; numberofpages:230; http://hdl.handle.net/11567/945741; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85091135605

الاتاحة: http://hdl.handle.net/11567/945741
https://doi.org/10.1017/9781108697019

المؤلفون: Mazzoli, M

المصدر: 100 Jahre Phoniatrie in Deutschland; 22. Jahrestagung der Deutschen Gesellschaft für Phoniatrie und Pädaudiologie, 24. Kongress der Union der Europäischen Phoniater; 20050916-20050918; Berlin; DOC05dgppHT04 /20050915/

مصطلحات موضوعية: ddc: 610

Relation: Balciuniene, J.; Dahl, N.; Borg, E.; Samuelsson, E.; Koisti, M. J.; Pettersson, U.; Jazin, E. E. : Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family. Am. J. Hum. Genet. 63: 786-793, 1998.; Bespalova, I. N.; Van Camp, G.; Bom, S. J. H.; Brown, D. J.; Cryns, K.; DeWan, A. T.; Erson, A. E.; Flothmann, K.; Kunst, H. P. M.; Kurnool, P.; Sivakumaran, T. A.; Cremers, C. W. R. J.; Leal, S. M.; Burmeister, M.; Lesperance, M. M. : Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Hum. Molec. Genet. 10: 2501-2508, 2001.; Blanton, S. H.; Liang, C. Y.; Cai, M. W.; Pandya, A.; Du, L. L.; Landa, B.; Mummalanni, S.; Li, K. S.; Chen, Z. Y.; Qin, X. N.; Liu, Y. F.; Balkany, T.; Nance, W. E.; Liu, X. Z. : A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter. J. Med. Genet. 39: 567-570, 2002.; Brown, M. R.; Tomek, M. S.; Van Laer, L.; Smith, S.; Kenyon, J. B.; Van Camp, G.; Smith, R. J. H. : A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA13, maps to chromosome 6p. Am. J. Hum. Genet. 61: 924-927, 1997.; Bykhovskaya Y, Estivill X, Taylor K Hang T, Hamon M, Casano RA, Yang H, Rotter JI Shohat M, Fischel-Ghodsian N. Candidate locus for a nuclear modifier gene for maternally inherited deafness. Am J Hum Genet. Jun;66(6):1905-10, 2000.; Chaib, H.; Place, C.; Salem, N.; Chardenoux, S.; Vincent, C.; Weissenbach, J.; El-Zir, E.; Loiselet, J.; Petit, C.: A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23. Hum. Molec. Genet. 5: 155-158, 1996.; Chen, A. H.; Ni, L.; Fukushima, K.; Marietta, J.; O'Neill, M.; Coucke, P.; Willems, P.; Smith, R. J. H. : Linkage of a gene for dominant non-syndromic deafness to chromosome 19. Hum. Molec. Genet. 4: 1073-1076, 1995.; Coucke, P.; Van Camp, G.; Djoyodiharjo, B.; Smith, S. D.; Frants, R. R.; Padberg, G. W.; Darby, J. K.; Huizing, E. H.; Cremers, C. W. R. J.; Kimberling, W. J.; Oostra, B. A.; Van de Heyning, P. H.; Willems, P. J. : Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families. New Eng. J. Med. 331: 425-431, 1994.; Cremers CWRJ and Smith RJH. Genetic hearing impairment. Its clinical presentations. In Advances in Oto-Rhino-Laryngology. Cremers CWRJ and Smith RJH Eds. Karger, Basel 2002. vol. 61.; DeWan, A. T.; Parrado, A. R.; Leal, S. M. : A second kindred linked to DFNA20 (17q25.3) reduces the genetic interval. Clin. Genet. 63: 39-45, 2003.; Donaudy, F.; Snoeckx, R.; Pfister, M.; Zenner, H.-P.; Blin, N.; Di Stazio, M.; Ferrara, A.; Lanzara, C.; Ficarella, R.; Declau, F.; Pusch, C. M.; Nurnberg, P.; Melchionda, S.; Zelante, L.; Ballana, E.; Estivill, X.; Van Camp, G.; Gasparini, P.; Savoia, A. : Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4). Am. J. Hum. Genet. 74: 770-776, 2004; Fagerheim, T.; Nilssen, O.; Raeymaekers, P.; Brox, V.; Moum, T.; Elverland, H. H.; Teig, E.; Omland, H. H.; Fostad, G. K.; Tranebjaerg, L. Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family. Hum. Molec. Genet. 5: 1187-1191, 1996.; Flex, E.; Mangino, M.; Mazzoli, M.; Martini, A.; Migliosi, V.; Colosimo, A.; Mingarelli, R.; Pizzuti, A.; Dallapiccola, B. : Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12. J. Med. Genet. 40: 278-282, 2003.; Fukushima, K.; Kasai, N.; Ueki, Y.; Nishizaki, K.; Sugata, K.; Hirakawa, S.; Masuda, A.; Gunduz, M.; Ninomiya, Y.; Masuda, Y.; Sato, M.; McGuirt, W. T.; Coucke, P.; Van Camp, G.; Smith, R. J. H. : A gene for fluctuating, progressive autosomal dominant nonsyndromic hearing loss, DFNA16, maps to chromosome 2q23-24.3. Am. J. Hum. Genet. 65: 141-150, 1999.; Greene, C. C.; McMillan, P. M.; Barker, S. E.; Kurnool, P.; Lomax, M. I.; Burmeister, M.; Lesperance, M. M. : DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24. Am. J. Hum. Genet. 68: 254-260, 2001.; Hafner, F. M.; Salam, A. A.; Linder, T. E.; Balmer, D.; Baumer, A.; Schinzel, A. A.; Spillmann, T.; Leal, S. M. : A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred. Am. J. Hum. Genet. 66: 1437-1442, 2000.; Kelley, P. M.; Abe, S.; Askew, J. W.; Smith, S. D.; Usami, S.; Kimberling, W. J. : Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12. Genomics 62: 172-176, 1999.; Kelley, P. M.; Harris, D. J.; Comer, B. C.; Askew, J. W.; Fowler, T.; Smith, S. D.; Kimberling, W. J. : Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Am. J. Hum. Genet. 62: 792-799, 1998.; Kubisch, C.; Schroeder, B. C.; Friedrich, T.; Lutjohann, B.; El-Amraoui, A.; Marlin, S.; Petit, C.; Jentsch, T. J. : KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell 96: 437-446, 1999.; Kunst, H.; Marres, H.; Huygen, P.; Van Duijnhoven, G.; Krebsova, A.; Van Der Velde, S.; Reis, A.; Cremers, F.; Cremers, C. : Non-syndromic autosomal dominant progressive non-specific mid-frequency sensorineural hearing impairment with childhood to late adolescence onset (DFNA21). Clin. Otolaryng. 25: 45-54, 2000.; Kurima, K.; Peters. L. M.; Yang, Y.; Riazuddin, S.; Ahmed, Z. M.; Naz, S.; Arnaud, D.; Drury, S.; Mo, J.; Makishima, T.; Ghosh, M.; Menon, P. S. N.; and 13 others : Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nature Genet. 30: 277-284, 2002.; Lalwani, A. K.; Linthicum, F. H.; Wilcox, E. R.; Moore, J. K.; Walters, F. C.; San Agustin, T. B.; Mislinski, J.; Miller, M. R.; Sinninger, Y.; Attaie, A.; Luxford, W. M. : A five-generation family with late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration. Audiol. Neurootol. 2: 139-154, 1997.; Lalwani, A. K.; Goldstein, J. A.; Kelley, M. J.; Luxford, W.; Castelein, C. M.; Mhatre, A. N. Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9. Am. J. Hum. Genet. 67: 1121-1128, 2000.; Liu, X.-Z.; Walsh, J.; Tamagawa, Y.; Kitamura, K.; Nishizawa, M.; Steel, K. P.; Brown, S. D. M. : Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. (Letter) Nature Genet. 17: 268-269, 1997.; Lynch, E. D.; Lee, M. K.; Morrow, J. E.; Welcsh, P. L.; Leon, P. E.; King, M.-C. : Nonsyndromic deafness DFNA1 associated with mutation of the human homolog of the Drosophila gene diaphanous. Science 278: 1315-1318, 1997.; Mangino, M.; Flex, E.; Capon, F.; Sangiuolo, F.; Carraro, E.; Gualandi, F.; Mazzoli, M.; Martini, A.; Novelli, G.; Dallapiccola, B. : Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26. Europ. J. Hum. Genet. 9: 667-671, 2001.; Manolis, E. N.; Yandavi, N.; Nadol, J. B., Jr.; Eavey, R. D.; McKenna, M.; Rosenbaum, S.; Khetarpal, U.; Halpin, C.; Merchant, S. N.; Duyk, G. M.; MacRae, C.; Seidman, C. E.; Seidman, J. G. : A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13. Hum. Molec. Genet. 5: 1047-1050, 1996.; Mazzoli M, Newton V, Murgia A, Bitner-Glindzicz M, Gasparini P, Read A, Parving A. Guidelines and recommendations for testing of Cx26 mutations and interpretation of results. Int J Pediatr Otorhinolaryngol. 2004 Nov;68(11):1397-8.; Mazzoli M, Van Camp G, Newton V, Giabini N, Declau F, Parving A: Recommendations for the Description of Genetic and Audiological Data for Families with Nonsyndromic Hereditary Hearing Impairment. Audiological Medicine 2003;1: 148-150.; McGuirt, W. T.; Prasad, S. D.; Griffith, A. J.; Kunst, H. P. M.; Green, G. E.; Shpargel, K. B.; Runge, C.; Huybrechts, C.; Mueller, R. F.; Lynch, E.; King, M.-C.; Brunner, H. G.; Cremers, C. W. R. J.; Takanosu, M.; Li, S.-W.; Arita, M.; Mayne, R.; Prockop, D. J.; Van Camp, G.; Smith, R. J. H. : Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nature Genet. 23: 413-419, 1999.; Morell, R. J.; Friderici, K. H.; Wei, S.; Elfenbein, J. L.; Friedman, T. B.; Fisher, R. A. : A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25. Genomics 63: 1-6, 2000.; Mustapha, M.; Weil, D.; Chardenoux, S.; Elias, S.; El-Zir, E.; Beckmann, J. S.; Loiselet, J.; Petit, C. An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21. Hum. Molec. Genet. 8: 409-412, 1999.; Naz S, Alasti F, Mowjoodi A, Riazuddin S, Sanati MH, Friedman TB, Griffith AJ, Wilcox ER, Riazuddin S. Distinctive audiometric profile associated with DFNB21 alleles of TECTA. J Med Genet. May;40(5):360-3, 2003.; O'Neill, M. E.; Marietta, J.; Nishimura, D.; Wayne, S.; Van Camp, G.; Van Laer, L.; Negrini, C.; Wilcox, E. R.; Chen, A.; Fukushima, K.; Ni, L.; Sheffield, V. C.; Smith, R. J. H. : A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6. Hum. Molec. Genet. 5: 853-856, 1996.; Peters, L. M.; Anderson, D. W.; Griffith, A. J.; Grundfast, K. M.; San Agustin, T. B.; Madeo, A. C.; Friedman, T. B.; Morell, R. J. : Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28. Hum. Molec. Genet. 11: 2877-2885, 2002.; Riazzudin S, Castelein CM, Ahmed ZM, Lalwani AK, Mastroianni MA, Naz S, Smith TN, Liburd NA, Friedman TB, Griffith AJ, Riazzudin S, Wilcox ER. Dominant modifier DFNM1 suppresses recessive deafness DFNB26. Nat Genet, 26(4):431-434, 2000.; Richard, G.; Smith, L. E.; Bailey, R. A.; Itin, P.; Hohl, D.; Epstein, E. H., Jr.; DiGiovanna, J. J.; Compton, J. G.; Bale, S. J. : Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. Nature Genet. 20: 366-369, 1998.; Robertson, N. G.; Lu, L.; Heller, S.; Merchant, S. N.; Eavey, R. D.; McKenna, M.; Nadol, J. B., Jr.; Miyamoto, R. T.; Linthicum, F. H., Jr.; Neto, J. F. L.; Hudspeth, A. J.; Seidman, C. E.; Morton, C. C.; Seidman, J. G. : Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction. Nature Genet. 20: 299-303, 1998.; Salam, A. A.; Hafner, F. M.; Linder, T. E.; Spillmann, T.; Schinzel, A. A.; Leal, S. M. : A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred. Am. J. Hum. Genet. 66: 1984-1988, 2000.; Takeda, K.; Inoue, K.; Tanizawa, Y.; Matsuzaki, Y.; Oba, J.; Watanabe Y.; Shinoda, K.; Oka, Y. : WFS1 (Wolfram syndrome 1) gene product: predominant subcellular localization to endoplasmic reticulum in cultured cells and neuronal expression in rat brain. Hum. Molec. Genet. 10: 477-484, 2001.; Tamagawa, Y.; Kitamura, K.; Ishida, T.; Ishikawa, K.; Tanaka, H.; Tsuji, S.; Nishizawa, M. : A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene. Hum. Molec. Genet. 5: 849-852, 1996.; Vahava, O.; Morell, R.; Lynch, E. D.; Weiss, S.; Kagan, M. E.; Ahituv, N.; Morrow, J. E.; Lee, M. K.; Skvorak, A. B.; Morton, C. C.; Blumenfeld, A.; Frydman, M.; Friedman, T. B.; King, M.-C.; Avraham, K. B. : Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science 279: 1950-1954, 1998.; Van Camp, G.; Coucke, P.; Balemans, W.; Van Velzen, D.; Van de Bilt, C.; Van Laer, L.; Smith, R. J. H.; Fukushima, K.; Padberg, G. W.; Frants, R. R.; Van de Heyning, P.; Smith, S. D.; Huizing, E. H.; Willems, P. J. : Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15. Hum. Molec. Genet. 4: 2159-2163, 1995.; Van Laer, L.; Van Camp, G.; van Zuijlen, D.; Green, E. D.; Verstreken, M.; Schatteman, I.; Van de Heyning, P.; Balemans, W.; Coucke, P.; Greinwald, J. H.; Smith, R. J. H.; Huizing, E.; Willems, P. Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea. Europ. J. Hum. Genet. 5: 397-405, 1997.; Wayne, S.; Robertson, N. 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H.; Friderici, K. H. : Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26). Am. J. Hum. Genet. 73: 1082-1091, 2003.; http://www.egms.de/en/meetings/dgpp2005/05dgpp105.shtml

الاتاحة: http://www.egms.de/en/meetings/dgpp2005/05dgpp105.shtml

المؤلفون: Buechner, A, Beynon, A, Szyfter, W, Niemczyk, K, Hoppe, U, Hey, M, Brokx, J, Eyles, J, Van de Heyning, P, Paludetti, G, Zarowski, A, Quaranta, Q, Wesarg, T, Festen, J, Olze, H, Dhooge, I, Müller-Deile, J, Ramos, A, Roman, S, Piron, J P, Cuda, D, Burdo, S, Grolman, W, Roux Vaillard, S, Huarte, A, Frachet, B, Morera, C, Garcia-Ibáñez, L, Abels, D, Walger, M, Müller-Mazotta, J, Antonio Leone, C, Meyer, B, Dillier, N, Steffens, T, Gentine, A, Mazzoli, M, Rypkema, G, Killian, M, Smoorenburg, G

المصدر: Buechner, A; Beynon, A; Szyfter, W; Niemczyk, K; Hoppe, U; Hey, M; Brokx, J; Eyles, J; Van de Heyning, P; Paludetti, G; Zarowski, A; Quaranta, Q; Wesarg, T; Festen, J; Olze, H; Dhooge, I; Müller-Deile, J; Ramos, A; Roman, S; Piron, J P; Cuda, D; Burdo, S; Grolman, W; Roux Vaillard, S; Huarte, A; Frachet, B; Morera, C; Garcia-Ibáñez, L; Abels, D; Walger, M; Müller-Mazotta, J; Antonio Leone, C; Meyer, B; Dillier, N; Steffens, T; Gentine, A; Mazzoli, M; Rypkema, G; Killian, M; Smoorenburg, G (2011). Clinical evaluation of cochlear implant sound coding taking into account conjectural masking functions, ....

مصطلحات موضوعية: Clinic for Otorhinolaryngology, 610 Medicine & health

وصف الملف: application/pdf

Relation: https://www.zora.uzh.ch/id/eprint/53839/1/Buechner_etal_cim55_2011.pdf; urn:issn:1467-0100

الاتاحة: https://www.zora.uzh.ch/id/eprint/53839/
https://www.zora.uzh.ch/id/eprint/53839/1/Buechner_etal_cim55_2011.pdf
https://doi.org/10.1179/1754762811Y0000000009

المؤلفون: Van Laer, Lut, VAN EYKEN, E, FRANSEN, E, HUYGHE, Jeroen, TOPSAKAL, V, HENDRICKX, JJ, HANNULA, S, MAKI-TORKKO, E, JENSEN, M, DEMEESTER, K, BAUR, M, BONACONSA, A, MAZZOLI, M, ESPESO, A, VERBRUGGEN, KATIA, HUYGHE, JOKE, HUYGEN, P, KUNST, S, MANNINEN, M, KONINGS, A, DIAZ-LACAVA, AN, STEFFENS, M, WIENKER, TF, PYYKKO, I, CREMERS, CWRJ, KREMER, H, Dhooge, Ingeborg, STEPHENS, D, ORZAN, E, PFISTER, M, BILLE, M, PARVING, A, SORRI, M, VAN DE HEYNING, PH, VAN CAMP, G

المصدر: HUMAN MOLECULAR GENETICS ; ISSN: 0964-6906

مصطلحات موضوعية: Medicine and Health Sciences

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/390554; http://hdl.handle.net/1854/LU-390554; http://dx.doi.org/10.1093/hmg/ddm292; https://biblio.ugent.be/publication/390554/file/1133959

الاتاحة: https://biblio.ugent.be/publication/390554
http://hdl.handle.net/1854/LU-390554
https://doi.org/10.1093/hmg/ddm292
https://biblio.ugent.be/publication/390554/file/1133959

المؤلفون: Coniglio, S., Turchi, G., Giovannini, G., Mazzoli, M., Meletti, S., Vaudano, Anna Elisabetta

المصدر: Neurological Sciences; Jun2022, Vol. 43 Issue 6, p3979-3982, 4p, 1 Chart, 1 Graph

مصطلحات موضوعية: PARANEOPLASTIC syndromes, GUILLAIN-Barre syndrome, SMALL cell lung cancer, NEUROPATHY, CEREBELLUM degeneration, INTRAVENOUS therapy

المؤلفون: Van Eyken, E, Van Camp, G, Fransen, E, Topsakal, V, Hendrickx, J J, Demeester, K, Van de Heyning, P, Mäki-Torkko, E, Hannula, S, Sorri, M, Jensen, M, Parving, A, Bille, M, Baur, M, Pfister, M, Bonaconsa, A, Mazzoli, M, Orzan, E, Espeso, A, Stephens, D, Verbruggen, K, Huyghe, J, Dhooge, I, Huygen, P, Kremer, H, Cremers, C W R J, Kunst, S, Manninen, M, Pyykkö, I, Lacava, A, Steffens, M, Wienker, T F, Van Laer, L

مصطلحات موضوعية: Original articles

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/44/9/570; http://dx.doi.org/10.1136/jmg.2007.049205

الاتاحة: http://jmg.bmj.com/cgi/content/short/44/9/570
https://doi.org/10.1136/jmg.2007.049205