المؤلفون: Roberto De Masi, Stefania Orlando, Vincenzo Toni, Maria Carmela Costa

المصدر: International Journal of Molecular Sciences, Vol 24, Iss 3, p 2968 (2023)

مصطلحات موضوعية: parkinsonism, Fluphenazine, neurotoxicity, neuroleptics, extrapyramidal syndrome, memory loss, Biology (General), QH301-705.5, Chemistry, QD1-999

Relation: https://www.mdpi.com/1422-0067/24/3/2968; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/d8dd3732b88e46be95736176e6a16770

الاتاحة: https://doi.org/10.3390/ijms24032968
https://doaj.org/article/d8dd3732b88e46be95736176e6a16770

المؤلفون: Fevga, Christina, Tesson, Christelle, Carreras Mascaro, Ana, Courtin, Thomas, van Coller, Riaan, Sakka, Salma, Ferraro, Federico, Farhat, Nouha, Bardien, Soraya, Damak, Mariem, Carr, Jonathan, Ferrien, Mélanie, Boumeester, Valerie, Hundscheid, Jasmijn, Grillenzoni, Nicola, Kessissoglou, Irini A, Kuipers, Demy J S, Quadri, Marialuisa, Yves Agid, Mathieu Anheim, Michel Borg, Alexis Brice, Emmanuel Broussolle, Jean-Christophe Corvol, Philippe Damier, Luc Defebvre, Alexandra Dürr, Franck Durif, Jean Luc Houeto, Paul Krack, Stephan Klebe, Suzanne Lesage, Ebba Lohmann, Maria Martinez, Graziella Mangone, Louise-Laure Mariani, Pierre Pollak, Olivier Rascol, François Tison, Christine Tranchant, Marc Vérin, François Viallet, and Marie Vidailhet, Murat Emre, Hasmet Hanagasi, Basar Bilgic, Bedia Marangozoğlu, Mustapha Benmahdjoub, Mohammed Arezki, Sofiane A. Bouchetara, Traki Benhassine, Meriem Tazir, Mouna Ben Djebara, Riadh Gouider, Sawssan Ben Romdhan, Chokri Mhiri, Ahmed Bouhouche, Vincenzo Bonifati, Wim Mandemakers, Anneke J. A. Kievit, Agnita J. W. Boon, Joaquim J. Ferreira, Leonor Correia Guedes, Hasmet A. Hanagasi, Zeynep Tufekcioglu, Bülent Elibol, Okan Doğu, Murat Gultekin, Hsin F. Chien, Egberto Barbosa, Laura Bannach Jardim, Carlos R. M. Rieder, Hsiu-Chen Chang, Chin-Song Lu, Yah-Huei Wu-Chou, Tu-Hsueh Yeh, Leonardo Lopiano, Cristina Tassorelli, Claudio Pacchetti, Cristoforo Comi, Francesco Raudino, Laura Bertolasi, Michele Tinazzi, Alberto Bonizzato, Carlo Ferracci, Roberto Marconi, Marco Guidi, Marco Onofrj, Astrid Thomas, Nicola Vanacore, Giuseppe Meco, Edito Fabrizio, Giovanni Fabbrini, Alfredo Berardelli, Fabrizio Stocchi, Laura Vacca, Paolo Barone, Marina Picillo, Giuseppe De Michele, Chiara Criscuolo, Michele De Mari, Claudia Dell'Aquila, Giovanni Iliceto, Vincenzo Toni, Giorgio Trianni, Valeria Saddi, Gianni Cossu, Maurizio Melis, Corvol, Jean-Christophe, Mhiri, Chokri, Hassan, Bassem A, Breedveld, Guido J, Lesage, Suzanne, Mandemakers, Wim, Brice, Alexis, Bonifati, Vincenzo

المساهمون: Christina, Fevga, Christelle, Tesson, Ana, Carreras Mascaro, Thomas, Courtin, Riaan, van Coller, Salma, Sakka, Federico, Ferraro, Nouha, Farhat, Soraya, Bardien, Mariem, Damak, Jonathan, Carr, Mélanie, Ferrien, Valerie, Boumeester, Jasmijn, Hundscheid, Nicola, Grillenzoni, Irini A, Kessissoglou, Demy J S, Kuiper, Marialuisa, Quadri, Agid, Yve, Anheim, Mathieu, Borg, Michel, Brice, Alexi, Broussolle, Emmanuel, Corvol, Jean-Christophe, Damier, Philippe, Defebvre, Luc, Dürr, Alexandra, Durif, Franck, Luc Houeto, Jean, Krack, Paul, Klebe, Stephan, Lesage, Suzanne, Lohmann, Ebba, Martinez, Maria, Mangone, Graziella, Mariani, Louise-Laure, Pollak, Pierre, Rascol, Olivier, Tison, Françoi, Tranchant, Christine, Vérin, Marc, Viallet, Françoi, Marie Vidailhet, And, Emre, Murat, Hanagasi, Hasmet, Bilgic, Basar, Marangozoğlu, Bedia, Benmahdjoub, Mustapha, Arezki, Mohammed, Bouchetara, Sofiane A., Benhassine, Traki, Tazir, Meriem, Ben Djebara, Mouna, Gouider, Riadh, Ben Romdhan, Sawssan, Mhiri, Chokri, Bouhouche, Ahmed, Bonifati, Vincenzo, Mandemakers, Wim, Kievit, Anneke J. A., Boon, Agnita J. W., Ferreira, Joaquim J., Correia Guedes, Leonor, Hanagasi, Hasmet A., Tufekcioglu, Zeynep, Elibol, Bülent, Doğu, Okan, Gultekin, Murat, Chien, Hsin F., Barbosa, Egberto, Bannach Jardim, Laura, Rieder, Carlos R. M., Chang, Hsiu-Chen, Lu, Chin-Song, Wu-Chou, Yah-Huei, Yeh, Tu-Hsueh, Lopiano, Leonardo, Tassorelli, Cristina, Pacchetti, Claudio, Comi, Cristoforo, Raudino, Francesco, Bertolasi, Laura, Tinazzi, Michele, Bonizzato, Alberto, Ferracci, Carlo, Marconi, Roberto, Guidi, Marco, Onofrj, Marco, Thomas, Astrid, Vanacore, Nicola, Meco, Giuseppe, Fabrizio, Edito, Fabbrini, Giovanni, Berardelli, Alfredo, Stocchi, Fabrizio, Vacca, Laura, Barone, Paolo

مصطلحات موضوعية: PP2A, PPP2R4, PTPA, intellectual disability, parkinsonism

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/36073231; info:eu-repo/semantics/altIdentifier/wos/WOS:000928296000001; volume:146; issue:4; firstpage:1496; lastpage:1510; numberofpages:15; journal:BRAIN; https://hdl.handle.net/11562/1102226; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85152396974; https://doi.org/10.1093/brain/awac326

الاتاحة: https://hdl.handle.net/11562/1102226
https://doi.org/10.1093/brain/awac326

المؤلفون: L Grasso, Silvia Ramat, Simone Gallerini, Paolo Barone, G. Di Brigida, D. Fogli, Tommaso Scaravilli, M. Braga, Alessandra Nicoletti, M. Romeno, Paolo Martinelli, G. Gurgone, Cesare Colosimo, E. Pilleri, V. Sorbello, S. Amidei, F. Pennisi, Francesco Iemolo, Giorgio Trianni, Vincenzo Toni, E. Milan, Raffaele Palladino, D. Benincasa, Giovanni Pezzoli, M. G. Randisi, Alfredo Petrone, Arianna Guidubaldi, R. Alfano, Tania P. Avarello, A. Scaglioni, Anna Rita Bentivoglio, C. Modica, L. Ferigo, M. Manfredi, Domenico Consoli, Giuseppe Meco, Giampiero Volpe, S. Griffini, Francesca Morgante, R. Scala, G. Nordera, Angelo Antonini, G. Floris, Roberto Erro, R. Muoio, Salvatore Zappulla, Luigi Bartolomei, Edo Bottacchi, Antonio Pisani, V. Petretta, Giovanni Fabbrini, G. Ciacci, L. Maiello, G. Ceravolo, M. Di Giovanni, V. Nastasi, Rocco Quatrale, D. Tiple, Marcello Deriu, S. Lanfranchi, Marianna Capecci, Alberto Albanese, T. Cuomo, Francesco E. Pontieri, Vincenzo Moschella, G. Sciortino, F. A. De Falco, S. Biguzzi, Leonardo Lopiano, Marina Picillo, C. Alesi, D. De Gaspari, Michele Abrignani, Gabriella Santangelo, Fabrizio Stocchi, R. Luciano, M. Baratti, R. M. Giglia, Cesa Scaglione, B. Troianiello, Giovanni Abbruzzese, M. Mucchiut, F. Pepe, S. Zanini, L. Capus, N. Caravona, Giovanni Cossu, V. Agnetti, G. Albani, L. Kiferle, E. Giaccaglini, Roberto Marconi, M. Iellamo, R. Marano, D. Medici, Monica Ulivelli, G. A. Cocco, M. Perini, P. Del Dotto, Rosa M. Gaglio, Rodolfo Savica, C. Logi, G. Ciccarelli, P. Massimo, M. Pesare, Antonino Cannas, Roberto Ceravolo, P. Simone, Letterio Morgante, P. Soliveri, S. Meoni

المساهمون: Picillo, M., Palladino, R., Erro, R., Alfano, R., Colosimo, C., Marconi, R., Antonini, A., Barone, P., Morgante, L., Benincasa, D., Quatrale, R., Biguzzi, S., Braga, M., Ceravolo, G., Capecci, M., Meco, G., Caravona, N., Scala, R., De Falco, F. A., Pezzoli, G., De Gaspari, D., Bottacchi, E., Di Giovanni, M., Cannas, A., Floris, G., Gallerini, S., Grasso, L., Gaglio, R. M., Gurgone, G., Volpe, G., Zappulla, S., Ceravolo, R., Kiferle, L., Ramat, S., Meoni, S., Pisani, A., Moschella, V., Morgante, F., Savica, R., Pepe, F., Ciccarelli, G., Petretta, V., Giglia, R. M., Randisi, M. G., Iemolo, F., Avarello, T. P., Romeno, M., Santangelo, G., Stocchi, F., Sciortino, G., Sorbello, V., Nicoletti, A., Tiple, D., Fabbrini, G., Bentivoglio, A., Pontieri, F. E., Guidubaldi, A., Muoio, R., Toni, V., Del Dotto, P., Logi, C., Ciacci, G., Ulivelli, M., Perini, M., Lanfranchi, S., Griffini, S., Troianiello, B., Baratti, M., Amidei, S., Consoli, D., Iellamo, M., Cuomo, T., Scaglioni, A., Medici, D., Manfredi, M., Abbruzzese, G., Di Brigida, G., Cocco, G. A., Agnetti, V., Cossu, G., Deriu, M., Abrignani, M., Modica, C., Albani, G., Milan, E., Martinelli, P., Scaglione, C., Mucchiut, M., Zanini, S., Pennisi, F., Soliveri, P., Albanese, A., Massimo, P., Bartolomei, L., Capus, L., Ferigo, L., Marano, R., Nastasi, V., Luciano, R., Maiello, L., Simone, P., Fogli, D., Lopiano, L., Pesare, M., Nordera, G., Pilleri, E., Scaravilli, T., Giaccaglini, E., Alesi, C., Petrone, A., Trianni, G.

المصدر: Journal of Neurology

مصطلحات موضوعية: Male, Neurology, Parkinson's disease, Constipation, Heterogeneity, Parkinson, Phenotype, Prodromal, Sex, PROGRESSION, Disease, 0302 clinical medicine, Apathy, Neuroradiology, Original Communication, Cognition, Parkinson Disease, 030211 gastroenterology & hepatology, Female, medicine.symptom, NONMOTOR SYMPTOMS, Life Sciences & Biomedicine, PRIAMO study group, Human, medicine.medical_specialty, Clinical Neurology, Prodromal Symptoms, Prodromal Symptom, 03 medical and health sciences, Internal medicine, medicine, Humans, Clinical phenotype, Aged, Science & Technology, Neurology & Neurosurgery, business.industry, 1103 Clinical Sciences, Biomarker, medicine.disease, DYSFUNCTION, Biomarkers, Neurology (clinical), Neurosciences & Neurology, business, 1109 Neurosciences, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06fe15decc86532430b7688b9c723a44
http://hdl.handle.net/11570/3207766

المؤلفون: Marialuisa Quadri, Wim Mandemakers, Martyna M Grochowska, Roy Masius, Hanneke Geut, Edito Fabrizio, Guido J Breedveld, Demy Kuipers, Michelle Minneboo, Leonie J M Vergouw, Ana Carreras Mascaro, Ekaterina Yonova-Doing, Erik Simons, Tianna Zhao, Alessio B Di Fonzo, Hsiu-Chen Chang, Piero Parchi, Marta Melis, Leonor Correia Guedes, Chiara Criscuolo, Astrid Thomas, Rutger W W Brouwer, Daphne Heijsman, Angela M T Ingrassia, Giovanna Calandra Buonaura, Janneke P Rood, Sabina Capellari, Annemieke J Rozemuller, Marianna Sarchioto, Hsin Fen Chien, Nicola Vanacore, Simone Olgiati, Yah-Huei Wu-Chou, Tu-Hsueh Yeh, Agnita J W Boon, Susanne E Hoogers, Mehrnaz Ghazvini, Arne S IJpma, Wilfred F J van IJcken, Marco Onofrj, Paolo Barone, David J Nicholl, Andreas Puschmann, Michele De Mari, Anneke J Kievit, Egberto Barbosa, Giuseppe De Michele, Danielle Majoor-Krakauer, John C van Swieten, Frank J de Jong, Joaquim J Ferreira, Giovanni Cossu, Chin-Song Lu, Giuseppe Meco, Pietro Cortelli, Wilma D J van de Berg, Vincenzo Bonifati, Anneke J.A. Kievit, Agnita J.W. Boon, Janneke P.A Rood, Leonie J.M. Vergouw, Frank J. de Jong, John C. van Swieten, Francesco U.S. Mattace-Raso, Klaus L. Leenders, Joaquim J. Ferreira, Emil Ygland, Christer Nilsson, Hsin F. Chien, Laura Bannach Jardim, Carlos R.M. Rieder, Leonardo Lopiano, Cristina Tassorelli, Claudio Pacchetti, Giulio Riboldazzi, Giorgio Bono, Cristoforo Comi, Alessandro Padovani, Barbara Borroni, Francesco Raudino, Emiliana Fincati, Michele Tinazzi, Alberto Bonizzato, Carlo Ferracci, Alessio Dalla Libera, Giovanni Abbruzzese, Roberto Marconi, Marco Guidi, Giovanni Fabbrini, Alfredo Berardelli, Fabrizio Stocchi, Laura Vacca, Marina Picillo, Claudia Dell'Aquila, Gianni Iliceto, Vincenzo Toni, Giorgio Trianni, Monica Gagliardi, Grazia Annesi, Aldo Quattrone, Valeria Saddi, Gianni Cossu, Maurizio Melis

المساهمون: Quadri, Marialuisa, Mandemakers, Wim, Grochowska, Martyna M, Masius, Roy, Geut, Hanneke, Fabrizio, Edito, Breedveld, Guido J, Kuipers, Demy, Minneboo, Michelle, Vergouw, Leonie J M, Carreras Mascaro, Ana, Yonova-Doing, Ekaterina, Simons, Erik, Zhao, Tianna, Di Fonzo, Alessio B, Chang, Hsiu-Chen, Parchi, Piero, Melis, Marta, Correia Guedes, Leonor, Criscuolo, Chiara, Thomas, Astrid, Brouwer, Rutger W W, Heijsman, Daphne, Ingrassia, Angela M T, Calandra Buonaura, Giovanna, Rood, Janneke P, Capellari, Sabina, Rozemuller, Annemieke J, Sarchioto, Marianna, Fen Chien, Hsin, Vanacore, Nicola, Olgiati, Simone, Wu-Chou, Yah-Huei, Yeh, Tu-Hsueh, Boon, Agnita J W, Hoogers, Susanne E, Ghazvini, Mehrnaz, IJpma, Arne S, van IJcken, Wilfred F J, Onofrj, Marco, Barone, Paolo, Nicholl, David J, Puschmann, Andrea, De Mari, Michele, Kievit, Anneke J, Barbosa, Egberto, De Michele, Giuseppe, Majoor-Krakauer, Danielle, van Swieten, John C, de Jong, Frank J, Ferreira, Joaquim J, Cossu, Giovanni, Lu, Chin-Song, Meco, Giuseppe, Cortelli, Pietro, van de Berg, Wilma D J, Bonifati, Vincenzo, Netherlands Institute for Neuroscience (NIN), Amsterdam Neuroscience - Neurodegeneration, Neurology, Anatomy and neurosciences, Pathology, Clinical Genetics, Erasmus MC other, Cell biology, Developmental Biology, Ijpma, Arne S

المصدر: The Lancet Neurology, 17, 597-608. Lancet Publishing Group
The Lancet Neurology, 17(7), 597-608. Lancet Publishing Group
Lancet Neurology, 17(7), 597-608. Lancet Publishing Group
International Parkinsonism Genetics Network 2018, ' LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies : a genome-wide linkage and sequencing study ', The Lancet Neurology, vol. 17, no. 7, pp. 597-608 . https://doi.org/10.1016/S1474-4422(18)30179-0

مصطلحات موضوعية: Lewy Body Disease, Male, Pluripotent Stem Cells, 0301 basic medicine, Proband, Heterozygote, medicine.medical_specialty, Candidate gene, Parkinson's disease, Genetic Linkage, Disease, 03 medical and health sciences, 0302 clinical medicine, Genetic linkage, Internal medicine, medicine, Journal Article, Humans, Dementia, Family, RNA, Messenger, Family history, LDL-Receptor Related Proteins, Chromosomes, Human, Pair 14, Dementia with Lewy bodies, business.industry, Brain, Parkinson Disease, Middle Aged, medicine.disease, Pedigree, 030104 developmental biology, Italy, Female, Neurology (clinical), business, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0e6386fbddbbc669fd451323d5f8502
https://pure.eur.nl/en/publications/3a0201b7-ab58-4167-8432-f3c6b73b8801

المؤلفون: Tu Hsueh Yeh, V. Bonifati, Hsin Fen Chien, Marialuisa Quadri, Cristina Tassorelli, Giovanni Abbruzzese, Fabrizio Stocchi, Giovanni Cossu, Vincenzo Toni, Chin Song Lu, Edito Fabrizio, Giuseppe Meco, Michele De Mari, Joaquim J. Ferreira, Egberto Reis Barbosa, Hsiu Chen Chang, Valeria Saddi, Pietro Cortelli, Janneke P.M.A. Rood, Leonardo Lopiano, Astrid Thomas, Anneke J.A. Kievit, Guido J. Breedveld, Leonor Correia Guedes, Agnita J.W. Boon

المصدر: Movement Disorders. 32:302-304

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Neurology, Parkinson's disease, business.industry, Bioinformatics, medicine.disease, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Common cause and special cause, medicine, Neurology (clinical), business, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::46b306b1ab5f889c2214845ed38dc9ae
https://doi.org/10.1002/mds.26900

المؤلفون: Angelo Antonini, Roberto Marconi, Letterio Morgante, Salvatore Zappulla, Francesco Ernesto Pontieri, Silvia Ramat, Maria Gabriella Ceravolo, Giuseppe Meco, Giulio Cicarelli, Massimo Pederzoli, Michela Manfredi, Roberto Ceravolo, Marco Mucchiut, Giampiero Volpe, Giovanni Abbruzzese, Edo Bottacchi, Luigi Bartolomei, Giuseppe Ciacci, Antonino Cannas, Maria Giovanna Randisi, Alfredo Petrone, Mario Baratti, Vincenzo Toni, Giovanni Cossu, Paolo Del Dotto, Anna Rita Bentivoglio, Michele Abrignani, Rossana Scala, Franco Pennisi, Rocco Quatrale, Rosa Maria Gaglio, Alessandra Nicoletti, Michele Perini, Tania Avarello, Antonio Pisani, Augusto Scaglioni, Paolo Emilio Martinelli, Francesco Iemolo, Laura Ferigo, Pasqualino Simone, Paola Soliveri, Biagio Troianiello, Domenico Consoli, Alessandro Mauro, Leonardo Lopiano, Giuseppe Nastasi, Carlo Colosimo, BARONE, Paolo

المساهمون: Angelo, Antonini, Barone, Paolo, Roberto, Marconi, Letterio, Morgante, Salvatore, Zappulla, Francesco Ernesto, Pontieri, Silvia, Ramat, Maria Gabriella, Ceravolo, Giuseppe, Meco, Giulio, Cicarelli, Massimo, Pederzoli, Michela, Manfredi, Roberto, Ceravolo, Marco, Mucchiut, Giampiero, Volpe, Giovanni, Abbruzzese, Edo, Bottacchi, Luigi, Bartolomei, Giuseppe, Ciacci, Antonino, Canna, Maria Giovanna, Randisi, Alfredo, Petrone, Mario, Baratti, Vincenzo, Toni, Giovanni, Cossu, Paolo Del, Dotto, Anna Rita, Bentivoglio, Michele, Abrignani, Rossana, Scala, Franco, Pennisi, Rocco, Quatrale, Rosa Maria, Gaglio, Alessandra, Nicoletti, Michele, Perini, Tania, Avarello, Antonio, Pisani, Augusto, Scaglioni, Paolo Emilio, Martinelli, Francesco, Iemolo, Laura, Ferigo, Pasqualino, Simone, Paola, Soliveri, Biagio, Troianiello, Domenico, Consoli, Alessandro, Mauro, Leonardo, Lopiano, Giuseppe, Nastasi, Carlo, Colosimo

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000311674300015; volume:259; firstpage:2621; lastpage:2631; journal:JOURNAL OF NEUROLOGY; http://hdl.handle.net/11386/4577066; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84872114319

الاتاحة: http://hdl.handle.net/11386/4577066
https://doi.org/10.1007/s00415-012-6557-8

المؤلفون: BERARDELLI, Alfredo, E. Fabrizio, A. Thomas, Emiliana Fincati, Roberto Marconi, Michele Tinazzi, Guido J. Breedveld, Erik J. Simons, Hsin F. Chien, Joaquim J. Ferreira, Martin W. Horstink, Giovanni Abbruzzese, Barbara Borroni, Giovanni Cossu, A. Dalla Libera, FABBRINI, Giovanni, Marco Guidi, Michele De Mari, Leonardo Lopiano, Emilia Martignoni, Paolo Marini, Marco Onofrj, Alessandro Padovani, Fabrizio Stocchi, Vincenzo Toni, Cristina Sampaio, Egberto R. Barbosa, MECO, Giuseppe, Genetics Network Italian Parkinson, Ben A. Oostra, Vincenzo Bonifati

المساهمون: Berardelli, Alfredo, E., Fabrizio, A., Thoma, Emiliana, Fincati, Roberto, Marconi, Michele, Tinazzi, Guido J., Breedveld, Erik J., Simon, Hsin F., Chien, Joaquim J., Ferreira, Martin W., Horstink, Giovanni, Abbruzzese, Barbara, Borroni, Giovanni, Cossu, A., Dalla Libera, Fabbrini, Giovanni, Marco, Guidi, Michele De, Mari, Leonardo, Lopiano, Emilia, Martignoni, Paolo, Marini, Marco, Onofrj, Alessandro, Padovani, Fabrizio, Stocchi, Vincenzo, Toni, Cristina, Sampaio, Egberto R., Barbosa, Meco, Giuseppe, Genetics Network Italian, Parkinson, Ben A., Oostra, Vincenzo, Bonifati

مصطلحات موضوعية: genetic, gigyf2, mutation, park11, parkinson's disease

Relation: info:eu-repo/semantics/altIdentifier/pmid/19482505; info:eu-repo/semantics/altIdentifier/wos/WOS:000272073300017; volume:15; issue:9; firstpage:703; lastpage:705; numberofpages:3; journal:PARKINSONISM & RELATED DISORDERS; http://hdl.handle.net/11573/118955; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-70350276499; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000272073300017&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.scopus.com/inward/record.url?eid=2-s2.0-70350276499&partnerID=65&md5=d06bd1886a99e9b0ac81ebc0da9c3905

الاتاحة: http://hdl.handle.net/11573/118955
https://doi.org/10.1016/j.parkreldis.2009.05.001
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000272073300017&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.scopus.com/inward/record.url?eid=2-s2.0-70350276499&partnerID=65&md5=d06bd1886a99e9b0ac81ebc0da9c3905

المؤلفون: Alessio Di Fonzo, Cristina Tassorelli, Michele De Mari, Hsin F. Chien, Joaquim Ferreira, Christan F. Rohe, Giulio Riboldazzi, Angelo Antonini, Gianni Albani, Alessandro Mauro, Roberto Marconi, Giovanni Abbruzzese, Leonardo Lopiano, Emiliana Fincati, Marco Guidi, Paolo Marini, Fabrizio Stocchi, Marco Onofrj, Vincenzo Toni, Michele Tinazzi, Paolo Lamberti, Nicola Vanacore, Petra Leitner, Ryan J. Uitti, Zbigniew K. Wszolek, Thomas Gasser, Erik J. Simons, Guido J. Breedveld, Stefano Goldwurm, Gianni Pezzoli, Cristina Sampaio, Egberto Barbosa, Emilia Martignoni, Ben A. Oostra, Vincenzo Bonifati, Italian Parkinson'S Genetics Network, FABBRINI, Giovanni, MECO, Giuseppe

المساهمون: Alessio Di, Fonzo, Cristina, Tassorelli, Michele De, Mari, Hsin F., Chien, Joaquim, Ferreira, Christan F., Rohe, Giulio, Riboldazzi, Angelo, Antonini, Gianni, Albani, Alessandro, Mauro, Roberto, Marconi, Giovanni, Abbruzzese, Leonardo, Lopiano, Emiliana, Fincati, Marco, Guidi, Paolo, Marini, Fabrizio, Stocchi, Marco, Onofrj, Vincenzo, Toni, Michele, Tinazzi, Fabbrini, Giovanni, Paolo, Lamberti, Nicola, Vanacore, Meco, Giuseppe, Petra, Leitner, Ryan J., Uitti, Zbigniew K., Wszolek, Thomas, Gasser, Erik J., Simon, Guido J., Breedveld, Stefano, Goldwurm, Gianni, Pezzoli, Cristina, Sampaio, Egberto, Barbosa, Emilia, Martignoni, Ben A., Oostra, Vincenzo, Bonifati, Italian Parkinson'S Genetics, Network

مصطلحات موضوعية: autosomal dominant, familial, lrrk2, mutation, park8, parkinson

Relation: info:eu-repo/semantics/altIdentifier/pmid/16333314; info:eu-repo/semantics/altIdentifier/wos/WOS:000235499300013; volume:14; issue:3; firstpage:322; lastpage:331; numberofpages:10; journal:EUROPEAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11573/235963; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33645139675; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000235499300013&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.scopus.com/inward/record.url?eid=2-s2.0-33645139675&partnerID=65&md5=23e4a98c003a5a592782218e2b54ef7a

الاتاحة: http://hdl.handle.net/11573/235963
https://doi.org/10.1038/sj.ejhg.5201539
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000235499300013&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
http://www.scopus.com/inward/record.url?eid=2-s2.0-33645139675&partnerID=65&md5=23e4a98c003a5a592782218e2b54ef7a

المؤلفون: Angelo, Antonini, Paolo, Barone, Roberto, Marconi, Letterio, Morgante, Salvatore, Zappulla, Pontieri, FRANCESCO ERNESTO, Silvia, Ramat, Maria Gabriella Ceravolo, Meco, Giuseppe, Giulio, Cicarelli, Massimo, Pederzoli, Michela, Manfredi, Roberto, Ceravolo, Mucchiot, M., Giampiero, Volpe, Giovanni, Abbruzzese, Edo, Bottacchi, Luigi, Bartolomei, Giuseppe, Ciacci, Antonino, Cannas, Maria Giovanna Randisi, Alfredo, Petrone, Mario, Baratti, Vincenzo, Toni, Giovanni, Cossu, Del Dotto, P., Anna Rita Bentivoglio, Michele, Abrignani, Rossana, Scala, Franco, Pennisi, Rocco, Quatrale, Rosa Maria Gaglio, Zappia, M., Michele, Perini, Tania, Avarello, Stanzione, P., Augusto, Scaglioni, Paolo Emilio Martinelli, Francesco, Iemolo, Laura, Ferigo, Pasqualino, Simone, Soliveri, L., Troianello, B., Domenico, Consoli, Alessandro, Mauro, Leonardo, Lopiano, Giuseppe, Nastasi, Colosimo, Carlo, Behalf Of The Priamo Study Group, O. N.

المصدر: Journal of neurology. 259(12)

مصطلحات موضوعية: Male, medicine.medical_specialty, Neurology, Parkinson's disease, Non-motor symptoms, Neurological disorder, Central nervous system disease, Cohort Studies, Disability Evaluation, Cognition, Quality of life, Internal medicine, medicine, 80 and over, Humans, Apathy, Prospective Studies, Mortality, Motor progression, Prospective cohort study, Aged, Aged, 80 and over, Motor Skills Disorders, Disease Progression, Quality of Life, Cross-Sectional Studies, Parkinson Disease, Follow-Up Studies, Middle Aged, Female, parkinson's disease, mortality, quality of life, cognition, motor progression, non-motor symptoms, business.industry, medicine.disease, Physical therapy, Parkinson’s disease, Settore MED/26 - Neurologia, Neurology (clinical), medicine.symptom, business, Motor deterioration

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f2635ba66e80d6087664b4ac002c3bd
https://pubmed.ncbi.nlm.nih.gov/22711157

المؤلفون: Ben A. Oostra, Alessandro Mauro, Giuseppe Meco, Joaquim J. Ferreira, Cristina Sampaio, Ryan J. Uitti, Emilia Martignoni, Michele Tinazzi, Marco Guidi, Gianni Pezzoli, Roberto Marconi, Cristina Tassorelli, Giovanni Fabbrini, Stefano Goldwurm, Zbigniew K. Wszolek, Leonardo Lopiano, P. Marini, Christan F. Rohé, Guido J. Breedveld, Vincenzo Bonifati, Marco Onofrj, Thomas Gasser, Giovanni Abbruzzese, Angelo Antonini, Erik J. Simons, Petra Leitner, Giulio Riboldazzi, Vincenzo Toni, G. Albani, Paolo Lamberti, Fabrizio Stocchi, Alessio Di Fonzo, E. Fincati, Nicola Vanacore, Michele De Mari, Hsin F. Chien, Egberto Reis Barbosa

المساهمون: Clinical Genetics

المصدر: European Journal of Human Genetics, 14(3), 322-331. Nature Publishing Group

مصطلحات موضوعية: Adult, Male, Proband, Parkinson, PARK8, LRRK2, familial, autosomal dominant, mutation, Heterozygote, medicine.medical_specialty, Genotype, Molecular Sequence Data, Protein Serine-Threonine Kinases, Biology, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, medicine.disease_cause, Open Reading Frames, Exon, Genetic linkage, Molecular genetics, Genetics, medicine, Animals, Humans, Amino Acid Sequence, Genetic Testing, Gene, Genetics (clinical), Aged, Genes, Dominant, lrrk2, park8, parkinson, Family Health, Mutation, Polymorphism, Genetic, Models, Genetic, Parkinson Disease, Exons, Middle Aged, Pedigree, Protein Structure, Tertiary, Alternative Splicing, Phenotype, Disease Progression, Medical genetics, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edff0e194ecd2195fde02d268d74751f
http://hdl.handle.net/2318/40925