المؤلفون: Corallo D., Frabetti S., Candini O., Gregianin E., Dominici M., Fischer H., Aveic S.

المساهمون: Corallo, D., Frabetti, S., Candini, O., Gregianin, E., Dominici, M., Fischer, H., Aveic, S.

مصطلحات موضوعية: 3D in vitro model, drug screening, extracellular matrix, immunotherapy, neuroblastoma, pediatric oncology

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33324402; info:eu-repo/semantics/altIdentifier/wos/WOS:000597662600001; volume:11; firstpage:584214; lastpage:584220; journal:FRONTIERS IN IMMUNOLOGY; http://hdl.handle.net/11380/1239248Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85097378214

الإتاحة: https://doi.org/10.3389/fimmu.2020.584214Test
http://hdl.handle.net/11380/1239248Test

المؤلفون: Gregianin, E, Vazza, G, Scaramel, E, Boaretto, F, Vettori, A, Leonardi, E, Tosatto, S C E, Manara, R, Pegoraro, E, Mostacciuolo, M L

المساهمون: Gregianin, E, Vazza, G, Scaramel, E, Boaretto, F, Vettori, A, Leonardi, E, Tosatto, S C E, Manara, R, Pegoraro, E, Mostacciuolo, M L

مصطلحات موضوعية: ARSACS, linkage analysi, mutation identification, peripheral neuropathy, spastic paraplegia, Adult, Heat-Shock Protein, Homozygote, Human, Italy, Male, Middle Aged, Muscle Spasticity, Mutation, Missense, Paraplegia, Pedigree, Peripheral Nervous System Disease, Phenotype, Spinocerebellar Ataxia, Consanguinity

وصف الملف: ELETTRONICO

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/23800155; info:eu-repo/semantics/altIdentifier/wos/WOS:000325547600013; volume:20; issue:11; firstpage:1486; lastpage:1491; numberofpages:6; journal:EUROPEAN JOURNAL OF NEUROLOGY; http://hdl.handle.net/11562/1011069Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84885843727

الإتاحة: https://doi.org/10.1111/ene.12220Test
http://hdl.handle.net/11562/1011069Test

المؤلفون: Gregianin, E., Vazza, G., Scaramel, E., Boaretto, F., Vettori, A., Leonardi, E., Tosatto, S. C. E., Manara, R., Pegoraro, E., Mostacciuolo, M. L.

المصدر: European Journal of Neurology; Nov2013, Vol. 20 Issue 11, p1486-1491, 6p, 1 Diagram

مصطلحات موضوعية: PERIPHERAL neuropathy, PARAPLEGIA, ATAXIA, GENETIC mutation, MAGNETIC resonance imaging of the brain, FAMILIAL diseases, ITALIANS