المؤلفون: Nicita F., Ginevrino M., Travaglini L., D'Arrigo S., Zorzi G., Borgatti R., Terrone G., Catteruccia M., Vasco G., Brankovic V., Siliquini S., Romano S., Veredice C., Pedemonte M., Armando M., Lettori D., Stregapede F., Bosco L., Sferra A., Tessarollo V., Romaniello R., Ristori G., Bertini E., Valente E. M., Zanni G.

المساهمون: Nicita, F., Ginevrino, M., Travaglini, L., D'Arrigo, S., Zorzi, G., Borgatti, R., Terrone, G., Catteruccia, M., Vasco, G., Brankovic, V., Siliquini, S., Romano, S., Veredice, C., Pedemonte, M., Armando, M., Lettori, D., Stregapede, F., Bosco, L., Sferra, A., Tessarollo, V., Romaniello, R., Ristori, G., Bertini, E., Valente, E. M., Zanni, G.

مصطلحات موضوعية: Central nervous system disease, cerebellar disease, genetic heterogeneity, neurodegenerative disease, neurology

Relation: info:eu-repo/semantics/altIdentifier/pmid/32737135; info:eu-repo/semantics/altIdentifier/wos/WOS:000680409100005; journal:JOURNAL OF MEDICAL GENETICS; https://hdl.handle.net/11573/1473001; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85093677649

الاتاحة: https://hdl.handle.net/11573/1473001
https://doi.org/10.1136/jmedgenet-2020-107007

المؤلفون: Imbrici P., Conte E., Blunck R., Stregapede F., Liantonio A., Tosi M., D'adamo M. C., De Luca A., Brankovic V., Zanni G.

المساهمون: Imbrici, P., Conte, E., Blunck, R., Stregapede, F., Liantonio, A., Tosi, M., D'Adamo, M. C., De Luca, A., Brankovic, V., Zanni, G.

مصطلحات موضوعية: 4-aminopyridine (4-AP), Ataxia, Epilepsy, KCNA2, Molecular dynamic, Patch clamp, 4-Aminopyridine, Amino Acid Sequence, Brain, Cerebellar Ataxia, Child, Preschool, Human, Infant, Kv1.2 Potassium Channel, Magnetic Resonance Imaging, Male, Molecular Dynamics Simulation, Young Adult

Relation: info:eu-repo/semantics/altIdentifier/pmid/34576077; volume:22; issue:18; firstpage:9913; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/11586/378669; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85114775937

الاتاحة: http://hdl.handle.net/11586/378669
https://doi.org/10.3390/ijms22189913

المؤلفون: Colasuonno F., Niceforo A., Marioli C., Fracassi A., Stregapede F., Massey K., Tartaglia M., Bertini E., Compagnucci C., Moreno S.

المساهمون: Colasuonno, F., Niceforo, A., Marioli, C., Fracassi, A., Stregapede, F., Massey, K., Tartaglia, M., Bertini, E., Compagnucci, C., Moreno, S.

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000565231700004; volume:2020; firstpage:6821247; numberofpages:19; journal:OXIDATIVE MEDICINE AND CELLULAR LONGEVITY; http://hdl.handle.net/11590/371855; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85090021443

الاتاحة: http://hdl.handle.net/11590/371855
https://doi.org/10.1155/2020/6821247

المؤلفون: Garone G., Capuano A., Travaglini L., Graziola F., Stregapede F., Zanni G., Vigevano F., Bertini E., Nicita F.

المساهمون: Garone, G., Capuano, A., Travaglini, L., Graziola, F., Stregapede, F., Zanni, G., Vigevano, F., Bertini, E., Nicita, F.

مصطلحات موضوعية: Acetazolamide, Ataxia, Basal ganglia, Cerebellum, Dyskinesia, Epilepsy, Functional movement disorder, Hyperkinetic movement disorder, Therapy, Whole exome sequencing, Chorea, Genetic Testing, Human, Mutation, Phenotype

Relation: info:eu-repo/semantics/altIdentifier/pmid/32443735; info:eu-repo/semantics/altIdentifier/wos/WOS:000539312100199; volume:21; issue:10; firstpage:3603; journal:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; http://hdl.handle.net/11573/1656379; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085265781

الاتاحة: http://hdl.handle.net/11573/1656379
https://doi.org/10.3390/ijms21103603

المؤلفون: Nicita F., Ginevrino M., Travaglini L., D'Arrigo S., Zorzi G., Borgatti R., Terrone G., Catteruccia M., Vasco G., Brankovic V., Siliquini S., Romano S., Veredice C., Pedemonte M., Armando M., Lettori D., Stregapede F., Bosco L., Sferra A., Tessarollo V., Romaniello R., Ristori G., Bertini E., Valente E. M., Zanni G.

المساهمون: Nicita, F., Ginevrino, M., Travaglini, L., D'Arrigo, S., Zorzi, G., Borgatti, R., Terrone, G., Catteruccia, M., Vasco, G., Brankovic, V., Siliquini, S., Romano, S., Veredice, C., Pedemonte, M., Armando, M., Lettori, D., Stregapede, F., Bosco, L., Sferra, A., Tessarollo, V., Romaniello, R., Ristori, G., Bertini, E., Valente, E. M., Zanni, G.

مصطلحات موضوعية: Central nervous system disease, cerebellar disease, genetic heterogeneity, neurodegenerative disease, neurology

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/32737135; firstpage:jmedgenet-2020-107007; journal:JOURNAL OF MEDICAL GENETICS; http://hdl.handle.net/11571/1450714; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85093677649

الاتاحة: http://hdl.handle.net/11571/1450714
https://doi.org/10.1136/jmedgenet-2020-107007

المؤلفون: Graziola F., Garone G., Stregapede F., Bosco L., Vigevano F., Curatolo P., Bertini E., Travaglini L., Capuano A.

المساهمون: Graziola, F, Garone, G, Stregapede, F, Bosco, L, Vigevano, F, Curatolo, P, Bertini, E, Travaglini, L, Capuano, A

مصطلحات موضوعية: children, chorea, dystonia, genetic, myoclonu, neurodegeneration with brain iron accumulation disorder, neurotransmitter, next-generation sequencing, Settore MED/39 - NEUROPSICHIATRIA INFANTILE

Relation: info:eu-repo/semantics/altIdentifier/pmid/31737037; info:eu-repo/semantics/altIdentifier/wos/WOS:000496133200001; volume:10; issue:OCT; firstpage:1026; journal:FRONTIERS IN GENETICS; http://hdl.handle.net/2108/230409; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85074775652

الاتاحة: http://hdl.handle.net/2108/230409
https://doi.org/10.3389/fgene.2019.01026

المؤلفون: Graziola F., Stregapede F., Travaglini L., Garone G., Verardo M., Bosco L., Pro S., Bertini E., Curatolo P., Vigevano F., Capuano A.

المساهمون: Graziola, F., Stregapede, F., Travaglini, L., Garone, G., Verardo, M., Bosco, L., Pro, S., Bertini, E., Curatolo, P., Vigevano, F., Capuano, A.

مصطلحات موضوعية: Child neurology, Dystonia, KCTD17, Myoclonus

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000468719900002; volume:61; firstpage:4; lastpage:6; numberofpages:3; journal:PARKINSONISM & RELATED DISORDERS; https://hdl.handle.net/11573/1656377

الاتاحة: https://hdl.handle.net/11573/1656377
https://doi.org/10.1016/j.parkreldis.2018.12.001

المؤلفون: Graziola, F., Garone, G., Stregapede, F., Bosco, L., Vigevano, F., Curatolo, P., Bertini, E., Travaglini, L., Capuano, A.

المساهمون: Graziola, F., Garone, G., Stregapede, F., Bosco, L., Vigevano, F., Curatolo, P., Bertini, E., Travaglini, L., Capuano, A.

مصطلحات موضوعية: children, chorea, dystonia, genetic, myoclonu, neurodegeneration with brain iron accumulation disorder, neurotransmitter, next-generation sequencing

Relation: info:eu-repo/semantics/altIdentifier/pmid/31737037; info:eu-repo/semantics/altIdentifier/wos/WOS:000496133200001; volume:10; issue:OCT; journal:FRONTIERS IN GENETICS; https://hdl.handle.net/11573/1656374

الاتاحة: https://hdl.handle.net/11573/1656374
https://doi.org/10.3389/fgene.2019.01026

المؤلفون: Nicita F., Stregapede F., Tessa A., Bassi M. T., Jezela-Stanek A., Primiano G., Pizzuti A., Barghigiani M., Nardella M., Zanni G., Servidei S., Astrea G., Panzeri E., Maghini C., Losito L., Ploski R., Gasperowicz P., Santorelli F. M., Bertini E., Travaglini L.

المساهمون: Nicita, F., Stregapede, F., Tessa, A., Bassi, M. T., Jezela-Stanek, A., Primiano, G., Pizzuti, A., Barghigiani, M., Nardella, M., Zanni, G., Servidei, S., Astrea, G., Panzeri, E., Maghini, C., Losito, L., Ploski, R., Gasperowicz, P., Santorelli, F. M., Bertini, E., Travaglini, L.

مصطلحات موضوعية: Hereditary spastic paraparesi, HSP, Leukodystrophy, SPG54, Thin corpus callosum, Adolescent, Brain, Child, Female, Genotype, Human, Male, Middle Aged, Phenotype, Phospholipase, Spastic Paraplegia, Hereditary, Young Adult

Relation: info:eu-repo/semantics/altIdentifier/pmid/31302745; info:eu-repo/semantics/altIdentifier/wos/WOS:000491432100006; volume:266; issue:11; firstpage:2657; lastpage:2664; numberofpages:8; journal:JOURNAL OF NEUROLOGY; http://hdl.handle.net/11573/1421955; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85068963136

الاتاحة: http://hdl.handle.net/11573/1421955
https://doi.org/10.1007/s00415-019-09466-y

المؤلفون: Stregapede, F., Meyer, A., Miall, C.

وصف الملف: application/pdf

Relation: http://hdl.handle.net/11858/00-001M-0000-0012-33D3-9; http://hdl.handle.net/11858/00-001M-0000-0012-33D2-B

الاتاحة: http://hdl.handle.net/11858/00-001M-0000-0012-33D3-9
http://hdl.handle.net/11858/00-001M-0000-0012-33D2-B

المؤلفون: Stregapede, F., Meyer, A., Miall, C.

وصف الملف: application/pdf

Relation: http://hdl.handle.net/11858/00-001M-0000-0012-33CF-4; http://hdl.handle.net/11858/00-001M-0000-0012-33CE-6

الاتاحة: http://hdl.handle.net/11858/00-001M-0000-0012-33CF-4
http://hdl.handle.net/11858/00-001M-0000-0012-33CE-6

المؤلفون: Stregapede, F., Meyer, A., Miall, C.

مصطلحات موضوعية: psy, socio

Relation: http://hdl.handle.net/11858/00-001M-0000-0012-33D3-9

الاتاحة: http://hdl.handle.net/11858/00-001M-0000-0012-33D3-9

المؤلفون: Stregapede, F., Meyer, A., Miall, C.

مصطلحات موضوعية: socio, psy

Relation: http://hdl.handle.net/11858/00-001M-0000-0012-33CF-4

الاتاحة: http://hdl.handle.net/11858/00-001M-0000-0012-33CF-4

المؤلفون: Stregapede, F., Meyer, A., Miall, C.

المصدر: PsycEXTRA Dataset

الاتاحة: http://dx.doi.org/10.1037/e512592013-453

المؤلفون: Nicita, Francesco, Aiello, Chiara, Vasco, Gessica, Valeriani, Massimiliano, Stregapede, Fabrizia, Sancesario, Andrea, Armando, Michela, Bertini, Enrico

المساهمون: Nicita, F, Aiello, C, Vasco, G, Valeriani, M, Stregapede, F, Sancesario, A, Armando, M, Bertini, E

مصطلحات موضوعية: DM20, HEMS, PLP1, Pelizaeus-Merzbacher disease, exon 3B, hypomyelinating, intron 3, leukodystrophy, proteolipid protein 1, Settore MED/39

Relation: info:eu-repo/semantics/altIdentifier/pmid/33450882; info:eu-repo/semantics/altIdentifier/wos/WOS:000609846600001; volume:11; issue:1; firstpage:1; lastpage:9; numberofpages:9; journal:BRAIN SCIENCES; https://hdl.handle.net/2108/363725; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85099347009

الاتاحة: https://hdl.handle.net/2108/363725
https://doi.org/10.3390/brainsci11010093

المؤلفون: Graziola, Federica, Stregapede, Fabrizia, Travaglini, Lorena, Garone, Giacomo, Verardo, Margherita, Bosco, Luca, Pro, Stefano, Bertini, Enrico, Curatolo, Paolo, Vigevano, Federico, Capuano, Alessandro

المساهمون: Graziola, F, Stregapede, F, Travaglini, L, Garone, G, Verardo, M, Bosco, L, Pro, S, Bertini, E, Curatolo, P, Vigevano, F, Capuano, A

مصطلحات موضوعية: Child neurology, Dystonia, KCTD17, Myoclonus, Settore MED/39 - NEUROPSICHIATRIA INFANTILE

Relation: info:eu-repo/semantics/altIdentifier/pmid/30579817; info:eu-repo/semantics/altIdentifier/wos/WOS:000468719900002; volume:61; firstpage:4; lastpage:6; numberofpages:3; journal:PARKINSONISM & RELATED DISORDERS; http://hdl.handle.net/2108/212740; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85064595562

الاتاحة: http://hdl.handle.net/2108/212740
https://doi.org/10.1016/j.parkreldis.2018.12.001

المؤلفون: Schirinzi, Tommaso, Graziola, Federica, Nicita, Francesco, Travaglini, Lorena, Stregapede, Fabrizia, Valeriani, Massimiliano, Curatolo, Paolo, Bertini, Enrico, Vigevano, Federico, Capuano, Alessandro

المساهمون: Schirinzi, T, Graziola, F, Nicita, F, Travaglini, L, Stregapede, F, Valeriani, M, Curatolo, P, Bertini, E, Vigevano, F, Capuano, A

مصطلحات موضوعية: AHC, ATP1A3, Ataxia, Cerebellum, Rapid-onset dystonia-parkinsonism, Settore MED/39

Relation: info:eu-repo/semantics/altIdentifier/pmid/29397530; info:eu-repo/semantics/altIdentifier/wos/WOS:000437113000012; volume:17; issue:4; firstpage:489; lastpage:493; numberofpages:5; journal:THE CEREBELLUM; https://hdl.handle.net/2108/365044; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85045153275

الاتاحة: https://hdl.handle.net/2108/365044
https://doi.org/10.1007/s12311-018-0920-y