المؤلفون: Di Fonzo A., Percetti M., Monfrini E., Palmieri I., Albanese A., Avenali M., Bartoletti-Stella A., Blandini F., Brescia G., Calandra Buonaura G., Campopiano R., Capellari S., Colangelo I., Comi G. P., Cuconato G., Ferese R., Galandra C., Gambardella S., Garavaglia B., Gaudio A., Giardina E., Invernizzi F., Mandich P., Mineri R., Panteghini C., Reale C., Trevisan L., Zampatti S., Cortelli P., Valente E. M., PARKNET study group, Baldelli L., Carelli V., Giannini G.

المساهمون: Di Fonzo A., Percetti M., Monfrini E., Palmieri I., Albanese A., Avenali M., Bartoletti-Stella A., Blandini F., Brescia G., Calandra Buonaura G., Campopiano R., Capellari S., Colangelo I., Comi G.P., Cuconato G., Ferese R., Galandra C., Gambardella S., Garavaglia B., Gaudio A., Giardina E., Invernizzi F., Mandich P., Mineri R., Panteghini C., Reale C., Trevisan L., Zampatti S., Cortelli P., Valente E.M., PARKNET study group, Baldelli L., Carelli V., Giannini G.

مصطلحات موضوعية: EOPD, gene panel, next-generation sequencing, Parkinson's disease, variant classification

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/37750340; info:eu-repo/semantics/altIdentifier/wos/WOS:001071591800001; volume:38; issue:12; firstpage:2241; lastpage:2248; numberofpages:8; journal:MOVEMENT DISORDERS; https://hdl.handle.net/11585/955745; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85172128841

الاتاحة: https://hdl.handle.net/11585/955745
https://doi.org/10.1002/mds.29617
https://movementdisorders.onlinelibrary.wiley.com/doi/full/10.1002/mds.29617

المؤلفون: Avenali M., Zangaglia R., Cuconato G., Palmieri I., Albanese A., Artusi C. A., Bozzali M., Calandra Buonaura G., Cavallieri F., Cilia R., Cocco A., Cogiamanian F., Colucci F., Cortelli P., Di Fonzo A., Eleopra R., Giannini G., Imarisio A., Imbalzano G., Ledda C., Lopiano L., Malaguti M. C., Mameli F., Minardi R., Mitrotti P., Monfrini E., Spagnolo F., Tassorelli C., Valentino F., Valzania F., Pacchetti C., Valente E. M.

المساهمون: Avenali M., Zangaglia R., Cuconato G., Palmieri I., Albanese A., Artusi C.A., Bozzali M., Calandra Buonaura G., Cavallieri F., Cilia R., Cocco A., Cogiamanian F., Colucci F., Cortelli P., Di Fonzo A., Eleopra R., Giannini G., Imarisio A., Imbalzano G., Ledda C., Lopiano L., Malaguti M.C., Mameli F., Minardi R., Mitrotti P., Monfrini E., Spagnolo F., Tassorelli C., Valentino F., Valzania F., Pacchetti C., Valente E.M.

مصطلحات موضوعية: COGNITION, ELECTRICAL STIMULATION, NEUROGENETICS, NEUROSURGERY, PARKINSON'S DISEASE

وصف الملف: ELETTRONICO

Relation: info:eu-repo/semantics/altIdentifier/pmid/37879897; info:eu-repo/semantics/altIdentifier/wos/WOS:001091225700001; volume:95; issue:4; firstpage:309; lastpage:315; numberofpages:7; journal:JOURNAL OF NEUROLOGY, NEUROSURGERY AND PSYCHIATRY; https://hdl.handle.net/11585/955123; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85175810426; https://jnnp.bmj.com/content/95/4/309

الاتاحة: https://hdl.handle.net/11585/955123
https://doi.org/10.1136/jnnp-2023-332387
https://jnnp.bmj.com/content/95/4/309

المؤلفون: Avenali M., Cerri S., Palmieri I., Ongari G., Stiuso R., Buongarzone G., Tassorelli C., Biagini T., Valente M., Cereda C., Mazza T., Gana S., Pacchetti C., Valente E. M.

المساهمون: Avenali, M., Cerri, S., Palmieri, I., Ongari, G., Stiuso, R., Buongarzone, G., Tassorelli, C., Biagini, T., Valente, M., Cereda, C., Mazza, T., Gana, S., Pacchetti, C., Valente, E. M.

مصطلحات موضوعية: Parkinson's disease, SNCA gene, functional characterization, glucocerebrosidase, α‐synuclein

Relation: info:eu-repo/semantics/altIdentifier/pmid/38436488; info:eu-repo/semantics/altIdentifier/wos/WOS:001178887900001; volume:39; issue:6; journal:MOVEMENT DISORDERS; https://hdl.handle.net/11573/1713902; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85187189169

الاتاحة: https://hdl.handle.net/11573/1713902
https://doi.org/10.1002/mds.29736

المؤلفون: Imarisio A., Pilotto A., Lupini A., Biasiotto G., Zanella I., Curro R., Vegezzi E., Cortese A., Palmieri I., Valente E. M., Padovani A.

المساهمون: Imarisio, A., Pilotto, A., Lupini, A., Biasiotto, G., Zanella, I., Curro, R., Vegezzi, E., Cortese, A., Palmieri, I., Valente, E. M., Padovani, A.

مصطلحات موضوعية: Aprataxin, APTX, Multiple system atrophy, Oculomotor apraxia, Parkinsonism

Relation: info:eu-repo/semantics/altIdentifier/pmid/38555792; volume:123; journal:PARKINSONISM & RELATED DISORDERS; https://hdl.handle.net/11571/1497662; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85189069047

الاتاحة: https://hdl.handle.net/11571/1497662
https://doi.org/10.1016/j.parkreldis.2024.106943

المؤلفون: Mitrotti, P., Avenali, M., Vegezzi, E., Zangaglia, R., Cortese, A., Currò, R., Pellerin, D., Dicaire, M.-J., Brais, B., Palmieri, I., Gana, S., Valente, E.M.

المصدر: Parkinsonism & Related Disorders ; volume 122, page 106782 ; ISSN 1353-8020

الاتاحة: http://dx.doi.org/10.1016/j.parkreldis.2024.106782
https://api.elsevier.com/content/article/PII:S1353802024007946?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1353802024007946?httpAccept=text/plain

المؤلفون: Gallo, L., Avenali, M., Caminiti, S., Mitrotti, P., Pocora, M., Cuconato, G., Palmieri, I., Pasquini, C., Galandra, C., Calabrese, R., Zangaglia, R., Tassorelli, C., Schapira, A.V.H., Valente, E.M., Blandini, F.

المصدر: Parkinsonism & Related Disorders ; volume 122, page 106158 ; ISSN 1353-8020

الاتاحة: http://dx.doi.org/10.1016/j.parkreldis.2024.106158
https://api.elsevier.com/content/article/PII:S1353802024001706?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1353802024001706?httpAccept=text/plain

المؤلفون: Junier, P., Cailleau, G., Palmieri, I., Vallotton, C., Trautschold, O.C., Junier, T., Paul, C., Bregnard, D., Palmieri, F., Estoppey, A., Buffi, M., Lohberger, A., Robinson, A., Kelliher, J.M., Davenport, K., House, G.L., Morales, D., Gallegos-Graves, V., Dichosa, AEK, Lupini, S., Nguyen, H.N., Young, J.D., Rodrigues, D.F., Parra-Vasquez, ANG, Bindschedler, S., Chain, PSG

المصدر: FEMS microbiology ecology, vol. 97, no. 2, pp. fiab003

مصطلحات موضوعية: Agaricales, Bacteria/genetics, Ecosystem, Fungi, Soil, Soil Microbiology, Coprinopsis, additive printing, bacteria–fungi interactions, horse dung

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/33440006; info:eu-repo/semantics/altIdentifier/eissn/1574-6941; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_5B9104AFFAAF1; https://serval.unil.ch/notice/serval:BIB_5B9104AFFAAF; https://serval.unil.ch/resource/serval:BIB_5B9104AFFAAF.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_5B9104AFFAAF
https://doi.org/10.1093/femsec/fiab003
https://serval.unil.ch/resource/serval:BIB_5B9104AFFAAF.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_5B9104AFFAAF1

المؤلفون: Percetti, M., Franco, G., Monfrini, E., Caporali, L., Minardi, R., La Morgia, C., Valentino, M. L., Liguori, R., Palmieri, I., Ottaviani, D., Vizziello, M., Ronchi, D., Di Berardino, F., Cocco, A., Macao, Bertil, 1969, Falkenberg, Maria, 1968, Comi, G. P., Albanese, A., Giometto, B., Valente, E. M., Carelli, V., Di Fonzo, A.

المصدر: Movement Disorders. 37(9):1938-1943

مصطلحات موضوعية: Neurosciences, Neurovetenskaper, TWNK, twinkle, Parkinson's disease, parkinsonism, mitochondrial DNA, progressive external ophthalmoplegia, onset spinocerebellar ataxia, familial parkinsonism, DNA deletions, mutations, polg, Neurosciences & Neurology

URL الوصول: https://gup.ub.gu.se/publication/319101

المؤلفون: Serpieri V., Mortarini G., Loucks H., Biagini T., Micalizzi A., Palmieri I., Dempsey J. C., D'Abrusco F., Mazzotta C., Battini R., Bertini E. S., Boltshauser E., Borgatti R., Brockmann K., D'Arrigo S., Nardocci N., Fischetto R., Agolini E., Novelli A., Romano A., Romaniello R., Stanzial F., Signorini S., Strisciuglio P., Gana S., Mazza T., Doherty D., Valente E. M.

المساهمون: Serpieri, V., Mortarini, G., Loucks, H., Biagini, T., Micalizzi, A., Palmieri, I., Dempsey, J. C., D'Abrusco, F., Mazzotta, C., Battini, R., Bertini, E. S., Boltshauser, E., Borgatti, R., Brockmann, K., D'Arrigo, S., Nardocci, N., Fischetto, R., Agolini, E., Novelli, A., Romano, A., Romaniello, R., Stanzial, F., Signorini, S., Strisciuglio, P., Gana, S., Mazza, T., Doherty, D., Valente, E. M.

مصطلحات موضوعية: Cerebellar Disease, Founder Effect, Gene Frequency, Genetic Carrier Screening, Genotype

Relation: info:eu-repo/semantics/altIdentifier/pmid/36788019; volume:60; issue:9; firstpage:885; lastpage:893; numberofpages:9; journal:JOURNAL OF MEDICAL GENETICS; https://hdl.handle.net/11571/1497644; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85159312262

الاتاحة: https://hdl.handle.net/11571/1497644
https://doi.org/10.1136/jmg-2022-108725

المؤلفون: De Michele G., Palmieri G. R., Pane C., Valente E. M., Palmieri I., Dello Iacovo C. D. P., Cuomo N., Giglio A., De Lucia N., Fico T., Perillo S., De Rosa A.

المساهمون: De Michele, G., Palmieri, G. R., Pane, C., Valente, E. M., Palmieri, I., Dello Iacovo, C. D. P., Cuomo, N., Giglio, A., De Lucia, N., Fico, T., Perillo, S., De Rosa, A.

مصطلحات موضوعية: Dementia, GBA gene, Non-motor symptom, Parkinson’ s disease, Psychosis

Relation: info:eu-repo/semantics/altIdentifier/pmid/36609835; volume:123; issue:1; firstpage:221; lastpage:226; numberofpages:6; journal:ACTA NEUROLOGICA BELGICA; https://hdl.handle.net/11571/1497642; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85145851946

الاتاحة: https://hdl.handle.net/11571/1497642
https://doi.org/10.1007/s13760-022-02165-y

المؤلفون: De Filippi P., Errichiello E., Toscano A., Mongini T., Moggio M., Ravaglia S., Filosto M., Servidei S., Musumeci O., Giannini F., Piperno A., Siciliano G., Ricci G., Di Muzio A., Rigoldi M., Tonin P., Croce M. G., Pegoraro E., Politano L., Maggi L., Telese R., Lerario A., Sancricca C., Vercelli L., Semplicini C., Pasanisi B., Bembi B., Dardis A., Palmieri I., Cereda C., Valente E. M., Danesino C.

المساهمون: De Filippi, P., Errichiello, E., Toscano, A., Mongini, T., Moggio, M., Ravaglia, S., Filosto, M., Servidei, S., Musumeci, O., Giannini, F., Piperno, A., Siciliano, G., Ricci, G., Di Muzio, A., Rigoldi, M., Tonin, P., Croce, M. G., Pegoraro, E., Politano, L., Maggi, L., Telese, R., Lerario, A., Sancricca, C., Vercelli, L., Semplicini, C., Pasanisi, B., Bembi, B., Dardis, A., Palmieri, I., Cereda, C., Valente, E. M., Danesino, C.

مصطلحات موضوعية: exonic variant, genetic modifier, genotype–phenotype correlate, glycogen catabolism, glycogen synthesi, late-onset Pompe disease (LOPD)

Relation: info:eu-repo/semantics/altIdentifier/pmid/37185710; info:eu-repo/semantics/altIdentifier/wos/WOS:000977779200001; volume:45; issue:4; firstpage:2847; lastpage:2860; numberofpages:14; journal:CURRENT ISSUES IN MOLECULAR BIOLOGY; https://hdl.handle.net/11571/1477494; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85153758430

الاتاحة: https://hdl.handle.net/11571/1477494
https://doi.org/10.3390/cimb45040186

المؤلفون: Brunetti S., Micheletti S., Palmieri I., Valente E. M., Fazzi E.

المساهمون: Brunetti, S., Micheletti, S., Palmieri, I., Valente, E. M., Fazzi, E.

مصطلحات موضوعية: chorea, dystonia, HPCA, hyperkinetic movement disorder

Relation: info:eu-repo/semantics/altIdentifier/pmid/36704070; info:eu-repo/semantics/altIdentifier/wos/WOS:000865478500001; volume:10; issue:1; firstpage:130; lastpage:134; numberofpages:5; journal:MOVEMENT DISORDERS CLINICAL PRACTICE; https://hdl.handle.net/11571/1477493; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85139453888

الاتاحة: https://hdl.handle.net/11571/1477493
https://doi.org/10.1002/mdc3.13572

المؤلفون: Petrucci S., Ginevrino M., Trezzi I., Monfrini E., Albanese A., Avenali M., Barone P., Bentivoglio A. R., Bonifati V., Bove F., Bonanni L., Brusa L., Cereda C., Cossu G., Criscuolo C., Dati G., De Rosa A., Eleopra R., Fabbrini G., Fadda L., Garbellini M., Minafra B., Onofrj M., Pacchetti C., Palmieri I., Pellecchia M. T., Petracca M., Picillo M., Pisani A., Vallelunga A., Zangaglia R., Di Fonzo A., Morgante F., Valente E. M., Ricciardi L.

المساهمون: Petrucci, S., Ginevrino, M., Trezzi, I., Monfrini, E., Albanese, A., Avenali, M., Barone, P., Bentivoglio, A. R., Bonifati, V., Bove, F., Bonanni, L., Brusa, L., Cereda, C., Cossu, G., Criscuolo, C., Dati, G., De Rosa, A., Eleopra, R., Fabbrini, G., Fadda, L., Garbellini, M., Minafra, B., Onofrj, M., Pacchetti, C., Palmieri, I., Pellecchia, M. T., Petracca, M., Picillo, M., Pisani, A., Vallelunga, A., Zangaglia, R., Di Fonzo, A., Morgante, F., Valente, E. M., Ricciardi, L.

مصطلحات موضوعية: dementia, GBA, genotype–phenotype correlate, impulsive–compulsive behavior, Parkinson's disease

Relation: info:eu-repo/semantics/altIdentifier/pmid/32658388; info:eu-repo/semantics/altIdentifier/wos/WOS:000547743300001; firstpage:1; lastpage:10; numberofpages:10; journal:MOVEMENT DISORDERS; https://hdl.handle.net/11386/4753625; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85087789720

الاتاحة: https://hdl.handle.net/11386/4753625
https://doi.org/10.1002/mds.28195

المؤلفون: Petrucci S, Ginevrino M, Trezzi I, Monfrini E, Ricciardi L, Albanese A, Avenali M, Barone P, Bentivoglio AR, Bonifati V, Bove F, Bonanni L, Brusa L, Cereda C, Cossu G, Criscuolo C, Dati G, De Rosa A, Eleopra R, Fabbrini G, Fadda L, Garbellini M, Minafra B, Onofrj M, Pacchetti C, Palmieri I, Pellecchia MT, Petracca M, Picillo M, Pisani A, Vallelunga A, Zangaglia R, Di Fonzo A, Morgante F, Valente EM, ITA-GENE-PD Study Group

المساهمون: Petrucci, S, Ginevrino, M, Trezzi, I, Monfrini, E, Ricciardi, L, Albanese, A, Avenali, M, Barone, P, Bentivoglio, A, Bonifati, V, Bove, F, Bonanni, L, Brusa, L, Cereda, C, Cossu, G, Criscuolo, C, Dati, G, De Rosa, A, Eleopra, R, Fabbrini, G, Fadda, L, Garbellini, M, Minafra, B, Onofrj, M, Pacchetti, C, Palmieri, I, Pellecchia, M, Petracca, M, Picillo, M, Pisani, A, Vallelunga, A, Zangaglia, R, Di Fonzo, A, Morgante, F, Valente, E, ITA-GENE-PD Study, G

مصطلحات موضوعية: Settore MED/05 - PATOLOGIA CLINICA

Relation: volume:35; issue:11; firstpage:2106; lastpage:2111; numberofpages:6; journal:MOVEMENT DISORDERS; http://hdl.handle.net/2108/275011; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85087789720

الاتاحة: http://hdl.handle.net/2108/275011

المؤلفون: Petrucci, S., Ginevrino, M., Trezzi, I., Monfrini, E., Ricciardi, L., Albanese, A., Avenali, M., Barone, P., Bentivoglio, A. R., Bonifati, V., Bove, F., Bonanni, L., Brusa, L., Cereda, C., Cossu, G., Criscuolo, C., Dati, G., De Rosa, A., Eleopra, R., Fabbrini, G., Fadda, L., Garbellini, M., Minafra, B., Onofrj, M., Pacchetti, C., Palmieri, I., Pellecchia, M. T., Petracca, M., Picillo, M., Pisani, A., Vallelunga, A., Zangaglia, R., Di Fonzo, A., Morgante, F., Valente, E. M., Altavista, M. C., Amboni, M., Ardolino, G., Berardelli, A., Cogiamanian, F., Colosimo, C., Costanti, D., De Michele, G., Bonaventura, C. D., Di Lazzaro, G., Di Lazzaro, V., Emanuele Elia, A., Erro, R., Ferrazzano, G., Guerra, A., Ialongo, T., Malaguti, M. C., Melis, M., Moro, E., Oppo, V., Ottaviani, D., Peluso, S., Quadri, M. L., Romito, L. M., Sarchioto, M., Schirinzi, T., Sorbera, C., Stefani, A., Thomas, A., Valente, M. L., Volpe, G, ITA-GENE-PD Study, Group.

المساهمون: Petrucci, S, Ginevrino, M, Trezzi, I, Monfrini, E, Ricciardi, L, Albanese, A, Avenali, M, Barone, P, Bentivoglio, Ar, Bonifati, V, Bove, F, Bonanni, L, Brusa, L, Cereda, C, Cossu, G, Criscuolo, C, Dati, G, De Rosa, A, Eleopra, R, Fabbrini, G, Fadda, L, Garbellini, M, Minafra, B, Onofrj, M, Pacchetti, C, Palmieri, I, Pellecchia, Mt, Petracca, M, Picillo, M, Pisani, A, Vallelunga, A, Zangaglia, R, Di Fonzo, A, Morgante, F, Valente, Em, Clinical Genetics, Erasmus MC other, Radiology & Nuclear Medicine

المصدر: Movement Disorders, 35(11), 2106-2111. John Wiley & Sons Inc.

مصطلحات موضوعية: 0301 basic medicine, Oncology, medicine.medical_specialty, Parkinson's disease, Genotype, genotype–phenotype correlates, Disease, Settore MED/05, Genotype phenotype, dementia, GBA, impulsive–compulsive behavior, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Internal medicine, medicine, Dementia, Humans, Sanger sequencing, business.industry, Dissection, Parkinson Disease, medicine.disease, Phenotype, Settore MED/26 - NEUROLOGIA, 030104 developmental biology, Glucosylceramidase, Italy, Mutation, Neurology, Cohort, symbols, Neurology (clinical), business, 030217 neurology & neurosurgery

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15201de07228c517e94cdeb076d6fa07
http://hdl.handle.net/11588/814735

المؤلفون: Petrucci, S, Ginevrino, M, Trezzi, I, Monfrini, E, Ricciardi, L, Albanese, A, Avenali, M, Barone, P, Bentivoglio, AR, Bonifati, V, Bove, F, Bonanni, L, Brusa, L, Cereda, C, Cossu, G, Criscuolo, C, Dati, G, De Rosa, A, Eleopra, R, Fabbrini, G, Fadda, L, Garbellini, M, Minafra, B, Onofrj, M, Pacchetti, C, Palmieri, I, Pellecchia, MT, Petracca, M, Picillo, M, Pisani, A, Vallelunga, A, Zangaglia, R, Di Fonzo, A, Morgante, F, Valente, EM

وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document; image/tiff

Relation: https://openaccess.sgul.ac.uk/id/eprint/112007/1/GBA%20Manuscript_14BR_%20Main%20document.docx; https://openaccess.sgul.ac.uk/id/eprint/112007/3/GBA%20Manuscript_14BR_Supplementary%20Material.docx; https://openaccess.sgul.ac.uk/id/eprint/112007/5/GBA%20Manuscript_14BR_Figure%201.tiff; https://openaccess.sgul.ac.uk/id/eprint/112007/10/GBA%20Manuscript_14BR_Figure%202.tiff; Petrucci, S; Ginevrino, M; Trezzi, I; Monfrini, E; Ricciardi, L; Albanese, A; Avenali, M; Barone, P; Bentivoglio, AR; Bonifati, V; et al. Petrucci, S; Ginevrino, M; Trezzi, I; Monfrini, E; Ricciardi, L; Albanese, A; Avenali, M; Barone, P; Bentivoglio, AR; Bonifati, V; Bove, F; Bonanni, L; Brusa, L; Cereda, C; Cossu, G; Criscuolo, C; Dati, G; De Rosa, A; Eleopra, R; Fabbrini, G; Fadda, L; Garbellini, M; Minafra, B; Onofrj, M; Pacchetti, C; Palmieri, I; Pellecchia, MT; Petracca, M; Picillo, M; Pisani, A; Vallelunga, A; Zangaglia, R; Di Fonzo, A; Morgante, F; Valente, EM (2020) GBA ‐Related Parkinson's Disease: Dissection of Genotype–Phenotype Correlates in a Large Italian Cohort. MOVEMENT DISORDERS, 35 (11). pp. 2106-2111. ISSN 0885-3185 https://doi.org/10.1002/mds.28195 SGUL Authors: Morgante, Francesca

الاتاحة: https://openaccess.sgul.ac.uk/id/eprint/112007/
https://openaccess.sgul.ac.uk/id/eprint/112007/1/GBA%20Manuscript_14BR_%20Main%20document.docx
https://openaccess.sgul.ac.uk/id/eprint/112007/3/GBA%20Manuscript_14BR_Supplementary%20Material.docx
https://openaccess.sgul.ac.uk/id/eprint/112007/5/GBA%20Manuscript_14BR_Figure%201.tiff
https://openaccess.sgul.ac.uk/id/eprint/112007/10/GBA%20Manuscript_14BR_Figure%202.tiff

المؤلفون: Petrucci, S., Ginevrino, M., Trezzi, I., Monfrini, E., Ricciardi, L., Albanese, A., Avenali, M., Barone, P., Bentivoglio, A. R., Bonifati, V., Bove, F., Bonanni, L., Brusa, L., Cereda, C., Cossu, G., Criscuolo, C., Dati, G., De Rosa, A., Eleopra, R., Fabbrini, G., Fadda, L., Garbellini, M., Minafra, B., Onofrj, M., Pacchetti, C., Palmieri, I., Pellecchia, M. T., Petracca, M., Picillo, M., Pisani, A., Vallelunga, A., Zangaglia, R., Di Fonzo, A., Morgante, F., Valente, E. M.

مصطلحات موضوعية: dementia, GBA, genotype–phenotype correlates, impulsive–compulsive behavior, Parkinson's disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3686::64dbdf18fee0f670d444c562b131beba
http://hdl.handle.net/11573/1433077

المؤلفون: Filippidou, S., Junier, T., Wunderlin, T., Kooli, W.M., Palmieri, I., Al-Dourobi, A., Molina, V., Lienhard, R., Spangenberg, J.E., Johnson, S. L., Chain, P.S.G., Dorador, C., Junier, P.

المصدر: Frontiers in Microbiology, vol. 10

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/30804904; info:eu-repo/semantics/altIdentifier/pissn/1664-302X; info:eu-repo/grantAgreement/SNF/////; https://serval.unil.ch/notice/serval:BIB_E248CF6E3112; https://serval.unil.ch/resource/serval:BIB_E248CF6E3112.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_E248CF6E3112
https://doi.org/10.3389/fmicb.2019.00102
https://serval.unil.ch/resource/serval:BIB_E248CF6E3112.P001/REF.pdf

المؤلفون: PALMIERI I, ROCCELLA, Michele, GARRO, Maria

المساهمون: PALMIERI I, ROCCELLA M, GARRO M

Relation: XIII Congresso Nazionale AIAMC - IX Congresso Latini Dies - Milano; volume:I; firstpage:107; lastpage:107; http://hdl.handle.net/10447/8200

الاتاحة: http://hdl.handle.net/10447/8200

المؤلفون: Filippidou, S., Jaussi, M., Junier, T., Wunderlin, T., Jeanneret, N., Palmieri, F., Palmieri, I., Roussel-Delif, L., Vieth-Hillebrand, A., Vetter, A., Chain, P., Regenspurg, S., Junier, P.

المصدر: International Journal of Systematic and Evolutionary Microbiology

Relation: info:eu-repo/semantics/altIdentifier/urn/http://doi.crossref.org/servlet/query?format=unixref&pid=bib@gfz-potsdam.de&id=10.1099/ijsem.0.001125; https://gfzpublic.gfz-potsdam.de/pubman/item/item_1856889

الاتاحة: https://gfzpublic.gfz-potsdam.de/pubman/item/item_1856889