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1دورية أكاديمية
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2دورية أكاديمية
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3دورية أكاديمية
المؤلفون: Barutello, G, Curcio, C, Spadaro, M, Arigoni, M, Trovato, R, Bolli, E, Zheng, YJ, Ria, F, Quaglino, E, Iezzi, M, Riccardo, F, Holmgren, L, Forni, G, Cavallo, F
المصدر: Oncoimmunology. 4(5):e1005500
مصطلحات موضوعية: Medicin och hälsovetenskap
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4دورية أكاديمية
المؤلفون: Evola S., Trovato R., Kauroo B., Alioto L., Sucato V., Quagliana A., Magro S., Tona R., Novo G., Andolina G., Assennato P., Novo S.
المصدر: Open Medicine, Vol 8, Iss 5, Pp 638-643 (2013)
مصطلحات موضوعية: patent foramen ovale, cryptogenic stroke, percutaneous closure, Medicine
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2391-5463
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المؤلفون: Bronte V, Ugel S, Tinazzi E, Vella A, De Sanctis F, Canè S, Batani V, Trovato R, Fiore A, Petrova V, Hofer F, Barouni RM, Musiu C, Caligola S, Pinton L, Torroni L, Polati E, Donadello K, Friso S, Pizzolo F, Iezzi M, Facciotti F, Pelicci PG, Righetti D, Bazzoni P, Rampudda M, Comel AC, Mosaner W, Lunardi C, Olivieri O.
المساهمون: Bronte, V, Ugel, S, Tinazzi, E, Vella, A, De Sanctis, F, Canè, S, Batani, V, Trovato, R, Fiore, A, Petrova, V, Hofer, F, Barouni, R, Musiu, C, Caligola, S, Pinton, L, Torroni, L, Polati, E, Donadello, K, Friso, S, Pizzolo, F, Iezzi, M, Facciotti, F, Pelicci, P, Righetti, D, Bazzoni, P, Rampudda, M, Comel, A, Mosaner, W, Lunardi, C, Olivieri, O
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1299::a6aaf8c5d88c793a27bd1d2736326983
http://hdl.handle.net/10281/335335 -
6دورية أكاديمية
المؤلفون: Luppi, MAff1, ID2403646_cor1, Trovato, R, Barozzi, P, Vallisa, D, Rossi, G, Re, A, Ravazzini, L, Potenza, L, Riva, G, Morselli, M, Longo, G, Cavanna, L, Roncaglia, R, Torelli, G
المصدر: Leukemia. 19(3):473-476
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7دورية أكاديمية
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8دورية أكاديمية
المؤلفون: Dominici, M, Campioni, D, Lanza, F, Luppi, M, Barozzi, P, Pauli, S, Milani, R, Cavazzini, F, Punturieri, M, Trovato, R, Torelli, G, Castoldi, GAff1, ID2401984_cor12
المصدر: Leukemia. 15(1):171-176
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المؤلفون: Astrea, G., Romano, A., Angelini, C., Antozzi, C. G., Barresi, R., Battini, R., Battisti, C., Bertini, E., Bruno, C., Cassandrini, D., Fanin, M., Fattori, F., Fiorillo, C., Guerrini, R., Maggi, L., Mercuri, E., Morani, F., Mora, M., Moro, F., Pezzini, I., Picillo, E., Pinelli, M., Politano, L., Rubegni, A., Sanseverino, W., Savarese, M., Striano, P., Torella, A., Trevisan, C. P., Trovato, R., Zaraieva, I., Muntoni, F., Nigro, V., D'Amico, A., Santorelli, F. M., Italian CMD Network, Berardinelli, A., Comi, G., Donati, M. A., Dotti, M., Grandis, M., Magri, F., Maioli, M. A., Malandrini, A., Mari, F., Massa, R., Merlini, L., Moggio, M., Morandi, L. O., Musumeci, O., Pane, M., Pini, A., Pegoraro, E., Pennisi, E. M., Peverelli, L., Ricci, G., Rodolico, C., Ruggiero, L., Sacchini, M., Santoro, L., Siciliano, G., Simonati, A., Tonin, P., Toscano, A.
المساهمون: Astrea, Guja, Romano, Alessandro, Angelini, Corrado, Antozzi, Carlo Giuseppe, Barresi, Rita, Battini, Roberta, Battisti, Carla, Bertini, Enrico, Bruno, Claudio, Cassandrini, Denise, Fanin, Marina, Fattori, Fabiana, Fiorillo, Chiara, Guerrini, Renzo, Maggi, Lorenzo, Mercuri, Eugenio, Morani, Federica, Mora, Marina, Moro, Francesca, Pezzini, Ilaria, Picillo, Esther, Pinelli, Michele, Politano, Luisa, Rubegni, Anna, Sanseverino, Walter, Savarese, Marco, Striano, Pasquale, Torella, Annalaura, Trevisan, Carlo Pietro, Trovato, Rosanna, Zaraieva, Irina, Muntoni, Francesco, Nigro, Vincenzo, D'Amico, Adele, Santorelli, Filippo M., Berardinelli, Angela, Comi, Giacomo, Donati, Maria Alice, Dotti, Maria Teresa, Grandis, Marina, Magri, Francesca, Maioli, Maria A, Malandrini, Alessandro, Mari, Francesco, Massa, Roberto, Merlini, Luciano, Moggio, Maurizio, Morandi, Lucia O, Musumeci, Olimpia, Pane, Marika, Pini, Antonella, Pegoraro, Elena, Pennisi, Elena M, Peverelli, Lorenzo, Ricci, Giulia, Rodolico, Carmelo, Ruggiero, Lucia, Sacchini, Michele, Santoro, Lucio, Siciliano, Gabriele, Simonati, Alessandro, Tonin, Paola, Toscano, Antonio, Astrea, G., Romano, A., Angelini, C., Antozzi, C. G., Barresi, R., Battini, R., Battisti, C., Bertini, E., Bruno, C., Cassandrini, D., Fanin, M., Fattori, F., Fiorillo, C., Guerrini, R., Maggi, L., Mercuri, E., Morani, F., Mora, M., Moro, F., Pezzini, I., Picillo, E., Pinelli, M., Politano, L., Rubegni, A., Sanseverino, W., Savarese, M., Striano, P., Torella, A., Trevisan, C. P., Trovato, R., Zaraieva, I., Muntoni, F., Nigro, V., D'Amico, A., Santorelli, F. M., Berardinelli, A., Comi, G., Donati, M. A., Dotti, M. T., Grandis, M., Magri, F., Maioli, M. A., Malandrini, A., Mari, F., Massa, R., Merlini, L., Moggio, M., Morandi, L. O., Musumeci, O., Pane, M., Pini, A., Pegoraro, E., Pennisi, E. M., Peverelli, L., Ricci, G., Rodolico, C., Ruggiero, L., Sacchini, M., Santoro, Lucio., Siciliano, G., Simonati, A., Tonin, P., Toscano, A., Department of Medical and Clinical Genetics, Medicum
المصدر: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)مصطلحات موضوعية: 0301 basic medicine, Male, Genotype-phenotype correlation, Dystriglycanopathies, lcsh:Medicine, GMPPB, Genotype-phenotype correlations, Dystroglycanopathie, Nucleotidyltransferase, Muscular Dystrophies, Limb-Girdle, 0302 clinical medicine, Missense mutation, Pharmacology (medical), Dystroglycan, Muscular dystrophy, Dystroglycans, Muscular Dystrophie, Genetics (clinical), Genetics, Arthrogryposis, education.field_of_study, 1184 Genetics, developmental biology, physiology, General Medicine, Middle Aged, Nucleotidyltransferases, Dystroglycanopathies, 3. Good health, Congenital muscular dystrophy, Female, Limb-girdle muscular dystrophy, medicine.symptom, Human, Adult, Population, Mutation, Missense, Genetic Association Studie, Biology, Settore MED/26, Aged, Cross-Sectional Studies, Genetic Association Studies, Humans, Muscular Dystrophies, Limb-Girdle, Mutation, Young Adult, 03 medical and health sciences, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, Congenital muscular dystrophy, Dystroglycanopathies, Genotype-phenotype correlations, GMPPB, Limb-girdle muscular dystrophy, Genetics (clinical), Pharmacology (medical), medicine, Congenital muscular dystrophy, Dystroglycanopathies, Genotype-phenotype correlations, GMPPB, Limb-girdle muscular dystrophy, Myopathy, education, SERVER, Cross-Sectional Studie, STABILITY, MUTATIONS, Genetic heterogeneity, Research, lcsh:R, medicine.disease, 030104 developmental biology, CONGENITAL MUSCULAR-DYSTROPHY, DEFECTIVE GLYCOSYLATION, 3111 Biomedicine, Missense, 030217 neurology & neurosurgery
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10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.