المؤلفون: Danielsson, A, Carecchio, M, Cif, L, Koy, A, Lin, JP, Solders, G, Romito, L, Lohmann, K, Garavaglia, B, Reale, C, Zorzi, G, Nardocci, N, Coubes, P, Gonzalez, V, Roubertie, A, Collod-Beroud, G, Lind, G, Tedroff, K

المصدر: Journal of clinical medicine. 8(12)

مصطلحات موضوعية: Medicin och hälsovetenskap

الوصول الحر: http://kipublications.ki.se/Default.aspx?queryparsed=id:142711185Test

المؤلفون: Nosadini M., Eyre M., Giacomini T., Valeriani M., Della Corte M., Praticò A. D., Annovazzi P., Cordani R., Cordelli D. M., Crichiutti G., Di Rosa G., Dolcemascolo V., Fetta A., Freri E., Gallo P., Gastaldi M., Granata T., Grazian L., Iorio R., Lombardini M., Margoni M., Mariotto S., Matricardi S., Melani F., Nardocci N., Papetti L., Passarini A., Pisani F., Po' C., Puthenparampil M., Ragona F., Savasta S., Siliquini S., Toldo I., Tozzo A., Turco E. C., Varone A., Vogrig A., Zuliani L., Bugin S., Rossato S., Orsini A., Cantalupo G., Mancardi M. M., Ferilli M. A. N., Foiadelli T., Sartori S.

المساهمون: Nosadini, M., Eyre, M., Giacomini, T., Valeriani, M., Della Corte, M., Praticò, A. D., Annovazzi, P., Cordani, R., Cordelli, D. M., Crichiutti, G., Di Rosa, G., Dolcemascolo, V., Fetta, A., Freri, E., Gallo, P., Gastaldi, M., Granata, T., Grazian, L., Iorio, R., Lombardini, M., Margoni, M., Mariotto, S., Matricardi, S., Melani, F., Nardocci, N., Papetti, L., Passarini, A., Pisani, F., Po', C., Puthenparampil, M., Ragona, F., Savasta, S., Siliquini, S., Toldo, I., Tozzo, A., Turco, E. C., Varone, A., Vogrig, A., Zuliani, L., Bugin, S., Rossato, S., Orsini, A., Cantalupo, G., Mancardi, M. M., Ferilli, M. A. N., Foiadelli, T., Sartori, S.

العلاقة: info:eu-repo/semantics/altIdentifier/wos/WOS:000913717200027; volume:10; issue:1; firstpage:e200065; journal:NEUROLOGY® NEUROIMMUNOLOGY & NEUROINFLAMMATION; https://hdl.handle.net/11390/1242624Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85146854043

الإتاحة: https://doi.org/10.1212/NXI.0000000000200065Test
https://hdl.handle.net/11390/1242624Test

المؤلفون: Garau J, Cavallera V, Valente M, Tonduti D, Sproviero D, Zucca S, Battaglia D, Battini R, Bertini E, Cappanera S, Chiapparini L, Crasà C, Crichiutti G, Giustina ED, D'Arrigo S, Giorgis V, Simone M, Galli J, Piana R, Messana T, Moroni I, Nardocci N, Panteghini C, Parazzini C, Pichiecchio A, Pini A, Ricci F, Saletti V, Salvatici E, Santorelli FM, Sartori S, Tinelli F, Uggetti C, Veneselli E, Zorzi G, Garavaglia B, Fazzi E, Orcesi S, Cereda C

المساهمون: Garau J, Cavallera V, Valente M, Tonduti D, Sproviero D, Zucca S, Battaglia D, Battini R, Bertini E, Cappanera S, Chiapparini L, Crasà C, Crichiutti G, Giustina ED, D'Arrigo S, Giorgis V, Simone M, Galli J, Piana R, Messana T, Moroni I, Nardocci N, Panteghini C, Parazzini C, Pichiecchio A, Pini A, Ricci F, Saletti V, Salvatici E, Santorelli FM, Sartori S, Tinelli F, Uggetti C, Veneselli E, Zorzi G, Garavaglia B, Fazzi E, Orcesi S, Cereda C

مصطلحات موضوعية: Aicardi-Goutières Syndrome, Interferon signature, Next Generation Sequencing

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31130681; info:eu-repo/semantics/altIdentifier/wos/WOS:000470992500185; volume:8; firstpage:1; lastpage:19; numberofpages:19; journal:JOURNAL OF CLINICAL MEDICINE; http://hdl.handle.net/2318/1806651Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85074273585

الإتاحة: https://doi.org/10.3390/jcm8050750Test
http://hdl.handle.net/2318/1806651Test

المؤلفون: Tinelli F., Nava S., Arioli F., Bedini G., Scelzo E., Lisini D., Farago G., Gioppo A., Ciceri E. F., Acerbi F., Ferroli P., Vetrano I. G., Esposito S., Saletti V., Pantaleoni C., Zibordi F., Nardocci N., Zedde M. L., Pezzini A., Lazzaro V. D., Capone F., Dell'acqua M. L., Vajkoczy P., Tournier-Lasserve E., Parati E. A., Bersano A., Gatti L.

المساهمون: F. Tinelli, S. Nava, F. Arioli, G. Bedini, E. Scelzo, D. Lisini, G. Farago, A. Gioppo, E.F. Ciceri, F. Acerbi, P. Ferroli, I.G. Vetrano, S. Esposito, V. Saletti, C. Pantaleoni, F. Zibordi, N. Nardocci, M.L. Zedde, A. Pezzini, V.D. Lazzaro, F. Capone, M.L. Dell'Acqua, P. Vajkoczy, E. Tournier-Lasserve, E.A. Parati, A. Bersano, L. Gatti

مصطلحات موضوعية: Endothelial progenitor cell, Moyamoya angiopathy, Neovascularization, RNF213, Settore BIO/10 - Biochimica, Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica, Settore BIO/11 - Biologia Molecolare, Settore MED/27 - Neurochirurgia, Settore MED/26 - Neurologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/32796702; info:eu-repo/semantics/altIdentifier/wos/WOS:000565157000001; volume:21; issue:16; firstpage:1; lastpage:22; numberofpages:22; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; https://hdl.handle.net/2434/946195Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85089486186

الإتاحة: https://doi.org/10.3390/ijms21165763Test
https://hdl.handle.net/2434/946195Test

المؤلفون: Balestrini, S, Mikati, MA, Garcia-Roves, RA, Carboni, M, Hunanyan, AS, Kherallah, B, McLean, M, Prange, L, De Grandis, E, Gagliardi, A, Pisciotta, L, Stagnaro, M, Veneselli, E, Campistol, J, Fons, C, Pias-Peleteiro, L, Brashear, A, Miller, C, Samoes, R, Brankovic, V, Padiath, QS, Potic, A, Pilch, J, Vezyroglou, K, Bye, AME, Davis, AM, Ryan, MM, Semsarian, C, Hollingsworth, G, Scheffer, IE, Granata, T, Nardocci, N, Ragona, F, Arzimanoglou, A, Panagiotakaki, E, Carrilho, I, Zucca, C, Novy, J, Dzieżyc, K, Parowicz, M, Mazurkiewicz-Bełdzińska, M, Weckhuysen, S, Pons, R, Groppa, S, Sinden, DS, Pitt, GS, Tinker, A, Ashworth, M, Michalak, Z, Thom, M, Cross, JH, Vavassori, R, Kaski, JP, Sisodiya, SM

المصدر: Neurology , 95 (21) e2866-e2879. (2020)

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10110385/1/e2866.full.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10110385Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10110385/1/e2866.full.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10110385Test/

المؤلفون: Steel, D, Zech, M, Zhao, C, Barwick, KE, Burke, D, Demailly, D, Kumar, KR, Zorzi, G, Nardocci, N, Kaiyrzhanov, R, Wagner, M, Iuso, A, Berutti, R, Škorvánek, M, Necpál, J, Davis, R, Wiethoff, S, Mankad, K, Sudhakar, S, Ferrini, A, Sharma, S, Kamsteeg, E-J, Tijssen, MA, Verschuuren, C, van Egmond, ME, Flowers, JM, McEntagart, M, Tucci, A, Genomics England Research Consortium, ., Coubes, P, Bustos, BI, Gonzalez-Latapi, P, Tisch, S, Darveniza, P, Gorman, KM, Peall, KJ, Bötzel, K, Koch, JC, Kmieć, T, Plecko, B, Boesch, S, Haslinger, B, Jech, R, Garavaglia, B, Wood, N, Houlden, H, Gissen, P, Lubbe, SJ, Sue, CM, Cif, L, Mencacci, NE, Anderson, G, Kurian, MA, Winkelmann, J

المصدر: Annals of Neurology , 88 (5) pp. 867-877. (2020)

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10108409/1/Barwick_ana.25879.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10108409Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10108409/1/Barwick_ana.25879.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10108409Test/

المؤلفون: Varley, JA, Bhatia, KP, Dale, RC, Fung, V, Granata, T, Tijssen, MAJ, Lang, A, Lin, J-P, Lim, M, Lynch, T, Nardocci, N, Sethi, KD, Irani, SR

العلاقة: https://ora.ox.ac.uk/objects/uuid:4d20781d-c833-4f93-934d-4e4dcce8df4fTest; https://doi.org/10.1002/mds.26689Test

الإتاحة: https://doi.org/10.1002/mds.26689Test
https://ora.ox.ac.uk/objects/uuid:4d20781d-c833-4f93-934d-4e4dcce8df4fTest

المؤلفون: Carecchio M., Mencacci N. E., Iodice A., Pons R., Panteghini C., Zorzi G., Zibordi F., Bonakis A., Dinopoulos A., Jankovic J., Stefanis L., Bhatia K. P., Monti V., R'Bibo L., Veneziano L., Garavaglia B., Fusco C., Wood N., Stamelou M., Nardocci N.

المساهمون: Carecchio, M., Mencacci, N. E., Iodice, A., Pons, R., Panteghini, C., Zorzi, G., Zibordi, F., Bonakis, A., Dinopoulos, A., Jankovic, J., Stefanis, L., Bhatia, K. P., Monti, V., R'Bibo, L., Veneziano, L., Garavaglia, B., Fusco, C., Wood, N., Stamelou, M., Nardocci, N.

مصطلحات موضوعية: ADCY5, Chorea, Dyskinesia, Dystonia, Myoclonu, Adenylyl Cyclase, Adolescent, Adult, Child, Preschool, Cohort Studie, DNA Mutational Analysi, Developmental Disabilitie, Female, Human, Male, Middle Aged, Mutation, Movement Disorders

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/28511835; info:eu-repo/semantics/altIdentifier/wos/WOS:000408297400006; volume:41; firstpage:37; lastpage:43; numberofpages:7; journal:PARKINSONISM & RELATED DISORDERS; http://hdl.handle.net/11577/3313769Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85018918319; www.elsevier.com/locate/parkreldis

الإتاحة: https://doi.org/10.1016/j.parkreldis.2017.05.004Test
http://hdl.handle.net/11577/3313769Test

المؤلفون: Nuovo S., Micalizzi A., Romaniello R., Arrigoni F., Ginevrino M., Casella A., Serpieri V., D'Arrigo S., Briguglio M., Salerno G. G., Rossato S., Sartori S., Leuzzi V., Battini R., Ben-Zeev B., Graziano C., Mirabelli Badenier M., Brankovic V., Nardocci N., Spiegel R., Petkovic RamadAa D., Vento G., Marti I., Simonati A., Dipresa S., Freri E., Mazza T., Bassi M. T., Bosco L., Travaglini L., Zanni G., Bertini E. S., Vanacore N., Borgatti R., Valente E. M.

المساهمون: Nuovo, S., Micalizzi, A., Romaniello, R., Arrigoni, F., Ginevrino, M., Casella, A., Serpieri, V., D'Arrigo, S., Briguglio, M., Salerno, G. G., Rossato, S., Sartori, S., Leuzzi, V., Battini, R., Ben-Zeev, B., Graziano, C., Mirabelli Badenier, M., Brankovic, V., Nardocci, N., Spiegel, R., Petkovic RamadAa, D., Vento, G., Marti, I., Simonati, A., Dipresa, S., Freri, E., Mazza, T., Bassi, M. T., Bosco, L., Travaglini, L., Zanni, G., Bertini, E. S., Vanacore, N., Borgatti, R., Valente, E. M.

مصطلحات موضوعية: and neonatal diseases and abnormalitie, cerebellar disease, congenital, genetic, genotype, hereditary, medical, phenotype

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34085948; info:eu-repo/semantics/altIdentifier/wos/WOS:000728642300001; volume:59; issue:4; firstpage:399; lastpage:409; numberofpages:11; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11577/3441337Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85102197986

الإتاحة: https://doi.org/10.1136/jmedgenet-2020-107497Test
http://hdl.handle.net/11577/3441337Test

المؤلفون: Paleari V., Nistico' V., Nardocci N., Canevini M. P., Priori A., Gambini O., Zorzi G., Demartini B.

المساهمون: Paleari, V, Nistico', V, Nardocci, N, Canevini, M, Priori, A, Gambini, O, Zorzi, G, Demartini, B

مصطلحات موضوعية: Functional neurological disorder, infant neuropsychiatry, paediatric conversion disorder, paediatric functional neurological disorder

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34743581; info:eu-repo/semantics/altIdentifier/wos/WOS:000716349400001; volume:27; issue:2; firstpage:492; lastpage:503; numberofpages:12; journal:CLINICAL CHILD PSYCHOLOGY AND PSYCHIATRY; https://hdl.handle.net/10281/456220Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85118542162

الإتاحة: https://doi.org/10.1177/13591045211055084Test
https://hdl.handle.net/10281/456220Test