Acoustic Properties of Absorbing Materials
2022-01-01 Piana, Ea; Bonfiglio, P; Rychtarikova, M
Uncertainty analysis of acoustic and non-acoustic parameters derived from four-microphone impedance tube measurements
2022-01-01 Roozen, Nb; Piana, Ea
Silencer Design for the Control of Low Frequency Noise in Ventilation Ducts
2022-01-01 Piana, Edoardo Alessio; Erik Carlsson, Ulf; Lezzi, Adriano Maria; Paderno, Diego; Boij, Susann
Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a GRN Mutation
2022-01-01 Cimini, Sara; Bellini, Sonia; Saraceno, Claudia; Benussi, Luisa; Ghidoni, Roberta; Giliani, Silvia Clara; Puoti, Gianfranco; Canafoglia, Laura; Giaccone, Giorgio; Rossi, Giacomina
Eye model for floaters’ studies: production of 3D printed scaffolds
2022-01-01 Riva, Leonardo; Mazzoldi, ELENA LAURA; Ginestra, Paola Serena; Ceretti, Elisabetta; Giliani, Silvia Clara
Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene
2019-01-01 Masneri, S.; Ferraro, R. M.; Lanzi, G.; Piovani, G.; Mori, L.; Barisani, C.; Moratto, D.; Plebani, A.; Badolato, R.; Soresina, A.; Giliani, S.
Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings
2022-01-01 Valeri, L; Lugli, L; Iughetti, L; Soresina, A; Giliani, S; Porta, F; Berardi, A.
CD40Lbase: A database of CD40L gene mutations causing X-linked hyper-IgM syndrome
1996-01-01 Notarangelo, L. D.; Peitsch, M. C.; Abrahamsen, T. G.; Bachelot, C.; Bordigoni, P.; Cant, A. J.; Chapel, H.; Clementi, M.; Deacock, S.; De Saint Basile, G.; Duse, M.; Espanol, T.; Etzioni, A.; Fasth, A.; Fischer, A.; Giliani, S.; Gomez, L.; Hammarstrom, L.; Jones, A.; Kanariou, M.; Kinnon, C.; Klemola, T.; Kroczek, R. A.; Levy, J.; Matamoros, N.; Monafo, V.; Paolucci, P.; Reznick, I.; Sanal, O.; Smith, C. I. E.; Thompson, R. A.; Tovo, P.; Villa, A.; Vihinen, M.; Vossen, J.; Zegers, B. J. M.; Ochs, H. D.; Conley, M. E.; Iseki, M.; Ramesh, N.; Shimadzu, M.; Saiki, O.
C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by Hyper IgM syndrome
1994-01-01 Villa, A.; Strina, D.; Macchi, P.; Patrosso, M. C.; Vezzoni, P.; Tovo, P. A.; Giliani, S.; Ugazio, A. G.; Notarangelo, L. D.
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group D
1994-01-01 Mondello, C.; Nardo, T.; Giliani, S.; Arrand, J. E.; Weber, C. A.; Lehmann, A. R.; Nuzzo, F.; Stefanini, M.
Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: Evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unit
1993-01-01 Mantuano 1, E; Candotti, F; Giliani, S; Parolini, O; Lusardi, M; Zucchi, M; Lanfranchi, A; Porta, F; Airò, P; Albertini, A; Et, Al.
Visuospatial Deficits Are Associated with Pisa Syndrome and not Camptocormia in Parkinson's Disease
2022-01-01 Artusi, C. A.; Montanaro, E.; Erro, R.; Margraf, N.; Geroin, C.; Pilotto, A.; Magistrelli, L.; Spagnolo, F.; Marchet, A.; Sarro, L.; Cuoco, S.; Sacchetti, M.; Riello, M.; Capellero, B.; Berchialla, P.; Moeller, B.; Vullriede, B.; Zibetti, M.; Rini, A. M.; Barone, P.; Comi, C.; Padovani, A.; Tinazzi, M.; Lopiano, L.
QEEG abnormalities in cognitively unimpaired patients with delirium
2022-01-01 Carrarini, Claudia; Calisi, Dario; Alessandro De Rosa, Matteo; Di Iorio, Angelo; D’Ardes, Damiano; Pellegrino, Raffaello; Gazzina, Stefano; Pilotto, Andrea; Arighi, Andrea; Carandini, Tiziana; Cagnin, Annachiara; Mozzetta, Stefano; Gallucci, Maurizio; Marco Bonifati, Domenico; Costa, Cinzia; D'Antonio, Fabrizia; Bruno, Giuseppe; Cipollone, Francesco; Babiloni, Claudio; Padovani, Alessandro; Onofrj, Marco; Bonanni, Laura
Differences between plasma and CSF p-tau181 and p-tau231 in early Alzheimer’s disease
2021-01-01 Pilotto, Andrea; Parigi, Marta; Bonzi, Giulio; Battaglio, Beatrice; Ferrari, Elisabetta; Mensi, Lorenza; Benussi, Alberto; Caratozzolo, Salvatore; Cosseddu, Maura; Turrone, Rosanna; Archetti, Silvana; J Ashton, Nicholas; Zetterberg, Henrik; Giliani, Silvia Clara; Padovani, Alessandro
Validation of α-Synuclein in L1CAM-Immunocaptured Exosomes as a Biomarker for the Stratification of Parkinsonian Syndromes
2021-01-01 Jiang, C; Hopfner, F; Berg, D; Hu, Mt; Pilotto, A; Borroni, B; Davis, Jj; Tofaris, Gk.
Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy
1993-01-01 Stefanini, M.; Lagomarsini, P.; Giliani, S.; Nardo, T.; Botta, E.; Peserico, A.; Kleijer, W. J.; Lehmann, A. R.; Sarasin, A.
Prognostic indicators and outcomes of hospitalised COVID-19 patients with neurological disease: An individual patient data meta-analysis
2022-01-01 Singh, B; Lant, S; Cividini, S; Cattrall, Jws; Goodwin, Lc; Benjamin, L; Michael, Bd; Khawaja, A; Matos, Amb; Alkeridy, W; Pilotto, A; Lahiri, D; Rawlinson, R; Mhlanga, S; Lopez, Ec; Sargent, Bf; Somasundaran, A; Tamborska, A; Webb, G; Younas, K; Al Sami, Y; Babu, H; Banks, T; Cavallieri, F; Cohen, M; Davies, E; Dhar, S; Fajardo Modol, A; Farooq, H; Harte, J; Hey, S; Joseph, A; Karthikappallil, D; Kassahun, D; Lipunga, G; Mason, R; Minton, T; Mond, G; Poxon, J; Rabas, S; Soothill, G; Zedde, M; Yenkoyan, K; Brew, B; Contini, E; Cysique, L; Zhang, X; Maggi, P; van Pesch, V; Lechien, J; Saussez, S; Heyse, A; Brito Ferreira, Ml; Soares, Cn; Elicer, I; Eugenín-von Bernhardi, L; Ñancupil Reyes, W; Yin, R; Azab, Ma; Abd-Allah, F; Elkady, A; Escalard, S; Corvol, Jc; Delorme, C; Tattevin, P; Bigaut, K; Lorenz, N; Hornuss, D; Hosp, J; Rieg, S; Wagner, D; Knier, B; Lingor, P; Winkler, As; Sharifi-Razavi, A; Moein, St; Seyedalinaghi, S; Jamalimoghadamsiahkali, S; Morassi, M; Padovani, A; Giunta, M; Libri, I; Beretta, S; Ravaglia, S; Foschi, M; Calabresi, P; Primiano, G; Servidei, S; Biagio Mercuri, N; Liguori, C; Pierantozzi, M; Sarmati, L; Boso, F; Garazzino, S; Mariotto, S; Patrick, Kn; Costache, O; Pincherle, A; Klok, Fa; Meza, R; Cabreira, V; Valdoleiros, Sr; Oliveira, V; Kaimovsky, I; Guekht, A; Koh, J; Fernández Díaz, E; Barrios-López, Jm; Guijarro-Castro, C; Beltrán-Corbellini, Á; Martínez-Poles, J; Diezma-Martín, Am; Morales-Casado, Mi; García García, S; Breville, G; Coen, M; Uginet, M; Bernard-Valnet, R; Du Pasquier, R; Kaya, Y; Abdelnour, Lh; Rice, C; Morrison, H; Defres, S; Huda, S; Enright, N; Hassell, J; D'Anna, L; Benger, M; Sztriha, L; Raith, E; Chinthapalli, K; Nortley, R; Paterson, R; Chandratheva, A; Werring, Dj; Dervisevic, S; Harkness, K; Pinto, A; Jillella, D; Beach, S; Padovani, A; Gunasekaran, K; Rocha Ferreira Da Silva, I; Nalleballe, K; Santoro, J; Scullen, T; Kahn, L; Kim, Cy; Thakur, Kt; Jain, R; Umapathi, T; Nicholson, Tr; Sejvar, Jj; Hodel, Em
Application of Molecular Analysis to Genetic Counseling in the Wiskott-Aldrich Syndrome (WAS)
1993-01-01 Notarangelo, L. D.; Candotti, F.; Parolini, O.; Mantuano, E.; Giliani, S.; Lanfranchi, A.; Albertini, A.
The Italian tremor Network (TITAN): rationale, design and preliminary findings
2022-01-01 Erro, R.; Pilotto, A.; Esposito, M.; Olivola, E.; Nicoletti, A.; Lazzeri, G.; Magistrelli, L.; Dallocchio, C.; Marchese, R.; Bologna, M.; Tessitore, A.; Misceo, S.; Gigante, A. F.; Terranova, C.; Moschella, V.; di Biase, L.; Di Giacopo, R.; Morgante, F.; Valentino, F.; De Rosa, A.; Trinchillo, A.; Malaguti, M. C.; Brusa, L.; Matinella, A.; Di Biasio, F.; Paparella, G.; De Micco, R.; Contaldi, E.; Modugno, N.; Di Fonzo, A.; Padovani, A.; Barone, P.
Correction to: The Italian tremor Network (TITAN): rationale, design and preliminary findings (Neurological Sciences, (2022), 10.1007/s10072-022-06104-w)
2022-01-01 Erro, R; Pilotto, A; Esposito, M; Olivola, E; Nicoletti, A; Lazzeri, G; Magistrelli, L; Dallocchio, C; Marchese, R; Bologna, M; Tessitore, A; Misceo, S; Gigante, Af; Terranova, C; Moschella, V; di Biase, L; Di Giacopo, R; Morgante, F; Valentino, F; De Rosa, A; Trinchillo, A; Malaguti, Mc; Brusa, L; Matinella, A; Di Biasio, F; Paparella, G; De Micco, R; Contaldi, E; Modugno, N; Di Fonzo, A; Padovani, A; Barone, P
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Acoustic Properties of Absorbing Materials | 1-gen-2022 | Piana, Ea; Bonfiglio, P; Rychtarikova, M | |
| Uncertainty analysis of acoustic and non-acoustic parameters derived from four-microphone impedance tube measurements | 1-gen-2022 | Roozen, Nb; Piana, Ea | |
| Silencer Design for the Control of Low Frequency Noise in Ventilation Ducts | 1-gen-2022 | Piana, Edoardo Alessio; Erik Carlsson, Ulf; Lezzi, Adriano Maria; Paderno, Diego; Boij, Susann | |
| Pathological 25 kDa C-Terminal Fragments of TDP-43 Are Present in Lymphoblastoid Cell Lines and Extracellular Vesicles from Patients Affected by Frontotemporal Lobar Degeneration and Neuronal Ceroidolipofuscinosis Carrying a GRN Mutation | 1-gen-2022 | Cimini, Sara; Bellini, Sonia; Saraceno, Claudia; Benussi, Luisa; Ghidoni, Roberta; Giliani, Silvia Clara; Puoti, Gianfranco; Canafoglia, Laura; Giaccone, Giorgio; Rossi, Giacomina | |
| Eye model for floaters’ studies: production of 3D printed scaffolds | 1-gen-2022 | Riva, Leonardo; Mazzoldi, ELENA LAURA; Ginestra, Paola Serena; Ceretti, Elisabetta; Giliani, Silvia Clara | |
| Generation of induced Pluripotent Stem Cells (UNIBSi008-A, UNIBSi008-B, UNIBSi008-C) from an Ataxia-Telangiectasia (AT) patient carrying a novel homozygous deletion in ATM gene | 1-gen-2019 | Masneri, S.; Ferraro, R. M.; Lanzi, G.; Piovani, G.; Mori, L.; Barisani, C.; Moratto, D.; Plebani, A.; Badolato, R.; Soresina, A.; Giliani, S. | |
| Omenn Syndrome due to RAG1 Mutation Presenting With Nonimmune Hydrops Fetalis in Two Siblings | 1-gen-2022 | Valeri, L; Lugli, L; Iughetti, L; Soresina, A; Giliani, S; Porta, F; Berardi, A. | |
| CD40Lbase: A database of CD40L gene mutations causing X-linked hyper-IgM syndrome | 1-gen-1996 | Notarangelo, L. D.; Peitsch, M. C.; Abrahamsen, T. G.; Bachelot, C.; Bordigoni, P.; Cant, A. J.; Chapel, H.; Clementi, M.; Deacock, S.; De Saint Basile, G.; Duse, M.; Espanol, T.; Etzioni, A.; Fasth, A.; Fischer, A.; Giliani, S.; Gomez, L.; Hammarstrom, L.; Jones, A.; Kanariou, M.; Kinnon, C.; Klemola, T.; Kroczek, R. A.; Levy, J.; Matamoros, N.; Monafo, V.; Paolucci, P.; Reznick, I.; Sanal, O.; Smith, C. I. E.; Thompson, R. A.; Tovo, P.; Villa, A.; Vihinen, M.; Vossen, J.; Zegers, B. J. M.; Ochs, H. D.; Conley, M. E.; Iseki, M.; Ramesh, N.; Shimadzu, M.; Saiki, O. | |
| C to T mutation causing premature termination of CD40 ligand at amino acid 221 in a patient affected by Hyper IgM syndrome | 1-gen-1994 | Villa, A.; Strina, D.; Macchi, P.; Patrosso, M. C.; Vezzoni, P.; Tovo, P. A.; Giliani, S.; Ugazio, A. G.; Notarangelo, L. D. | |
| Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group D | 1-gen-1994 | Mondello, C.; Nardo, T.; Giliani, S.; Arrand, J. E.; Weber, C. A.; Lehmann, A. R.; Nuzzo, F.; Stefanini, M. | |
| Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: Evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unit | 1-gen-1993 | Mantuano 1, E; Candotti, F; Giliani, S; Parolini, O; Lusardi, M; Zucchi, M; Lanfranchi, A; Porta, F; Airò, P; Albertini, A; Et, Al. | |
| Visuospatial Deficits Are Associated with Pisa Syndrome and not Camptocormia in Parkinson's Disease | 1-gen-2022 | Artusi, C. A.; Montanaro, E.; Erro, R.; Margraf, N.; Geroin, C.; Pilotto, A.; Magistrelli, L.; Spagnolo, F.; Marchet, A.; Sarro, L.; Cuoco, S.; Sacchetti, M.; Riello, M.; Capellero, B.; Berchialla, P.; Moeller, B.; Vullriede, B.; Zibetti, M.; Rini, A. M.; Barone, P.; Comi, C.; Padovani, A.; Tinazzi, M.; Lopiano, L. | |
| QEEG abnormalities in cognitively unimpaired patients with delirium | 1-gen-2022 | Carrarini, Claudia; Calisi, Dario; Alessandro De Rosa, Matteo; Di Iorio, Angelo; D’Ardes, Damiano; Pellegrino, Raffaello; Gazzina, Stefano; Pilotto, Andrea; Arighi, Andrea; Carandini, Tiziana; Cagnin, Annachiara; Mozzetta, Stefano; Gallucci, Maurizio; Marco Bonifati, Domenico; Costa, Cinzia; D'Antonio, Fabrizia; Bruno, Giuseppe; Cipollone, Francesco; Babiloni, Claudio; Padovani, Alessandro; Onofrj, Marco; Bonanni, Laura | |
| Differences between plasma and CSF p-tau181 and p-tau231 in early Alzheimer’s disease | 1-gen-2021 | Pilotto, Andrea; Parigi, Marta; Bonzi, Giulio; Battaglio, Beatrice; Ferrari, Elisabetta; Mensi, Lorenza; Benussi, Alberto; Caratozzolo, Salvatore; Cosseddu, Maura; Turrone, Rosanna; Archetti, Silvana; J Ashton, Nicholas; Zetterberg, Henrik; Giliani, Silvia Clara; Padovani, Alessandro | |
| Validation of α-Synuclein in L1CAM-Immunocaptured Exosomes as a Biomarker for the Stratification of Parkinsonian Syndromes | 1-gen-2021 | Jiang, C; Hopfner, F; Berg, D; Hu, Mt; Pilotto, A; Borroni, B; Davis, Jj; Tofaris, Gk. | |
| Genetic heterogeneity of the excision repair defect associated with trichothiodystrophy | 1-gen-1993 | Stefanini, M.; Lagomarsini, P.; Giliani, S.; Nardo, T.; Botta, E.; Peserico, A.; Kleijer, W. J.; Lehmann, A. R.; Sarasin, A. | |
| Prognostic indicators and outcomes of hospitalised COVID-19 patients with neurological disease: An individual patient data meta-analysis | 1-gen-2022 | Singh, B; Lant, S; Cividini, S; Cattrall, Jws; Goodwin, Lc; Benjamin, L; Michael, Bd; Khawaja, A; Matos, Amb; Alkeridy, W; Pilotto, A; Lahiri, D; Rawlinson, R; Mhlanga, S; Lopez, Ec; Sargent, Bf; Somasundaran, A; Tamborska, A; Webb, G; Younas, K; Al Sami, Y; Babu, H; Banks, T; Cavallieri, F; Cohen, M; Davies, E; Dhar, S; Fajardo Modol, A; Farooq, H; Harte, J; Hey, S; Joseph, A; Karthikappallil, D; Kassahun, D; Lipunga, G; Mason, R; Minton, T; Mond, G; Poxon, J; Rabas, S; Soothill, G; Zedde, M; Yenkoyan, K; Brew, B; Contini, E; Cysique, L; Zhang, X; Maggi, P; van Pesch, V; Lechien, J; Saussez, S; Heyse, A; Brito Ferreira, Ml; Soares, Cn; Elicer, I; Eugenín-von Bernhardi, L; Ñancupil Reyes, W; Yin, R; Azab, Ma; Abd-Allah, F; Elkady, A; Escalard, S; Corvol, Jc; Delorme, C; Tattevin, P; Bigaut, K; Lorenz, N; Hornuss, D; Hosp, J; Rieg, S; Wagner, D; Knier, B; Lingor, P; Winkler, As; Sharifi-Razavi, A; Moein, St; Seyedalinaghi, S; Jamalimoghadamsiahkali, S; Morassi, M; Padovani, A; Giunta, M; Libri, I; Beretta, S; Ravaglia, S; Foschi, M; Calabresi, P; Primiano, G; Servidei, S; Biagio Mercuri, N; Liguori, C; Pierantozzi, M; Sarmati, L; Boso, F; Garazzino, S; Mariotto, S; Patrick, Kn; Costache, O; Pincherle, A; Klok, Fa; Meza, R; Cabreira, V; Valdoleiros, Sr; Oliveira, V; Kaimovsky, I; Guekht, A; Koh, J; Fernández Díaz, E; Barrios-López, Jm; Guijarro-Castro, C; Beltrán-Corbellini, Á; Martínez-Poles, J; Diezma-Martín, Am; Morales-Casado, Mi; García García, S; Breville, G; Coen, M; Uginet, M; Bernard-Valnet, R; Du Pasquier, R; Kaya, Y; Abdelnour, Lh; Rice, C; Morrison, H; Defres, S; Huda, S; Enright, N; Hassell, J; D'Anna, L; Benger, M; Sztriha, L; Raith, E; Chinthapalli, K; Nortley, R; Paterson, R; Chandratheva, A; Werring, Dj; Dervisevic, S; Harkness, K; Pinto, A; Jillella, D; Beach, S; Padovani, A; Gunasekaran, K; Rocha Ferreira Da Silva, I; Nalleballe, K; Santoro, J; Scullen, T; Kahn, L; Kim, Cy; Thakur, Kt; Jain, R; Umapathi, T; Nicholson, Tr; Sejvar, Jj; Hodel, Em | |
| Application of Molecular Analysis to Genetic Counseling in the Wiskott-Aldrich Syndrome (WAS) | 1-gen-1993 | Notarangelo, L. D.; Candotti, F.; Parolini, O.; Mantuano, E.; Giliani, S.; Lanfranchi, A.; Albertini, A. | |
| The Italian tremor Network (TITAN): rationale, design and preliminary findings | 1-gen-2022 | Erro, R.; Pilotto, A.; Esposito, M.; Olivola, E.; Nicoletti, A.; Lazzeri, G.; Magistrelli, L.; Dallocchio, C.; Marchese, R.; Bologna, M.; Tessitore, A.; Misceo, S.; Gigante, A. F.; Terranova, C.; Moschella, V.; di Biase, L.; Di Giacopo, R.; Morgante, F.; Valentino, F.; De Rosa, A.; Trinchillo, A.; Malaguti, M. C.; Brusa, L.; Matinella, A.; Di Biasio, F.; Paparella, G.; De Micco, R.; Contaldi, E.; Modugno, N.; Di Fonzo, A.; Padovani, A.; Barone, P. | |
| Correction to: The Italian tremor Network (TITAN): rationale, design and preliminary findings (Neurological Sciences, (2022), 10.1007/s10072-022-06104-w) | 1-gen-2022 | Erro, R; Pilotto, A; Esposito, M; Olivola, E; Nicoletti, A; Lazzeri, G; Magistrelli, L; Dallocchio, C; Marchese, R; Bologna, M; Tessitore, A; Misceo, S; Gigante, Af; Terranova, C; Moschella, V; di Biase, L; Di Giacopo, R; Morgante, F; Valentino, F; De Rosa, A; Trinchillo, A; Malaguti, Mc; Brusa, L; Matinella, A; Di Biasio, F; Paparella, G; De Micco, R; Contaldi, E; Modugno, N; Di Fonzo, A; Padovani, A; Barone, P |
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