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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

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:131313412

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

URL الوصول: https://doaj.org/article/23973be89b4b4ace93586cf7c869632f

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

مصطلحات موضوعية: SARS-CoV-2, COVID-19 patients, cytokine storm, immune modulation, JAK/STAT

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______1299::a6aaf8c5d88c793a27bd1d2736326983
http://hdl.handle.net/10281/335335

المؤلفون: Luppi, M^{Aff1, 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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المؤلفون: Dominici, M, Campioni, D, Lanza, F, Luppi, M, Barozzi, P, Pauli, S, Milani, R, Cavazzini, F, Punturieri, M, Trovato, R, Torelli, G, Castoldi, G^{Aff1, ID2401984_cor12}

المصدر: Leukemia. 15(1):171-176

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

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97c387aaa6386176223215e1a8301fe0
https://pubmed.ncbi.nlm.nih.gov/30257713

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