Microtubule Destabilization Is Shared by Genetic and Idiopathic Parkinson’s Disease Patient Fibroblasts

Por Cartelli, Daniele, Goldwurm, Stefano, Casagrande, Francesca, Pezzoli, Gianni, Cappelletti, Graziella
Publicado em 2012

Correction: Microtubule Destabilization Is Shared by Genetic and Idiopathic Parkinson’s Disease Patient Fibroblasts

Por Cartelli, Daniele, Goldwurm, Stefano, Casagrande, Francesca, Pezzoli, Gianni, Cappelletti, Graziella
Publicado em 2012

Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson’s disease

Por Brighina, Laura, Riva, Chiara, Bertola, Francesca, Saracchi, Enrico, Fermi, Silvia, Goldwurm, Stefano, Ferrarese, Carlo
Publicado em 2013

Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease

Por Lautier, Corinne, Goldwurm, Stefano, Dürr, Alexandra, Giovannone, Barbara, Tsiaras, William G., Pezzoli, Gianni, Brice, Alexis, Smith, Robert J.
Publicado em 2008

Association analysis of PARP1 polymorphisms with Parkinson’s disease

Por Brighina, Laura, Riva, Chiara, Bertola, Francesca, Fermi, Silvia, Saracchi, Enrico, Piolti, Roberto, Goldwurm, Stefano, Pezzoli, Gianni, Ferrarese, Carlo
Publicado em 2011

Alpha-Synuclein Expression in the Oligodendrocyte Lineage: an In Vitro and In Vivo Study Using Rodent and Human Models

Por Djelloul, Mehdi, Holmqvist, Staffan, Boza-Serrano, Antonio, Azevedo, Carla, Yeung, Maggie S., Goldwurm, Stefano, Frisén, Jonas, Deierborg, Tomas, Roybon, Laurent
Publicado no Stem Cell Reports (2015)

GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling

Por Giovannone, Barbara, Tsiaras, William G., de la Monte, Suzanne, Klysik, Jan, Lautier, Corinne, Karashchuk, Galina, Goldwurm, Stefano, Smith, Robert J.
Publicado em 2009

SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

Por Trotta, Luca, Guella, Ilaria, Soldà, Giulia, Sironi, Francesca, Tesei, Silvana, Canesi, Margherita, Pezzoli, Gianni, Goldwurm, Stefano, Duga, Stefano, Asselta, Rosanna
Publicado em 2012

DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients()

Por Sironi, Francesca, Primignani, Paola, Ricca, Sara, Tunesi, Sara, Zini, Michela, Tesei, Silvana, Cilia, Roberto, Pezzoli, Gianni, Seia, Manuela, Goldwurm, Stefano
Publicado em 2013

Glucocerebrosidase mutations in primary parkinsonism

Por Asselta, Rosanna, Rimoldi, Valeria, Siri, Chiara, Cilia, Roberto, Guella, Ilaria, Tesei, Silvana, Soldà, Giulia, Pezzoli, Gianni, Duga, Stefano, Goldwurm, Stefano
Publicado no Parkinsonism Relat Disord (2014)

Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson's Disease and Other Movement Disorders

Por Castiglioni, Emanuela, Finazzi, Dario, Goldwurm, Stefano, Pezzoli, Gianni, Forni, Gianluca, Girelli, Domenico, Maccarinelli, Federica, Poli, Maura, Ferrari, Maurizio, Cremonesi, Laura, Arosio, Paolo
Publicado em 2010

Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases

Por Filocamo, Mirella, Baldo, Chiara, Goldwurm, Stefano, Renieri, Alessandra, Angelini, Corrado, Moggio, Maurizio, Mora, Marina, Merla, Giuseppe, Politano, Luisa, Garavaglia, Barbara, Casareto, Lorena, Bricarelli, Francesca Dagna
Publicado em 2013

Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study

Por Dumitriu, Alexandra, Pacheco, Chris D., Wilk, Jemma B., Strathearn, Katherine E., Latourelle, Jeanne C., Goldwurm, Stefano, Pezzoli, Gianni, Rochet, Jean-Christophe, Lindquist, Susan, Myers, Richard H.
Publicado em 2011

LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population

Por Cilia, Roberto, Siri, Chiara, Rusconi, Damiana, Allegra, Roberta, Ghiglietti, Andrea, Sacilotto, Giorgio, Zini, Michela, Zecchinelli, Anna L., Asselta, Rosanna, Duga, Stefano, Paganoni, Anna M., Pezzoli, Gianni, Seia, Manuela, Goldwurm, Stefano
Publicado em 2014

Genomewide association study for onset age in Parkinson disease

Por Latourelle, Jeanne C, Pankratz, Nathan, Dumitriu, Alexandra, Wilk, Jemma B, Goldwurm, Stefano, Pezzoli, Gianni, Mariani, Claudio B, DeStefano, Anita L, Halter, Cheryl, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana
Publicado em 2009

The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks

Por Baldo, Chiara, Casareto, Lorena, Renieri, Alessandra, Merla, Giuseppe, Garavaglia, Barbara, Goldwurm, Stefano, Pegoraro, Elena, Moggio, Maurizio, Mora, Marina, Politano, Luisa, Sangiorgi, Luca, Mazzotti, Raffaella, Viotti, Valeria, Meloni, Ilaria, Pellico, Maria Teresa, Barzaghi, Chiara, Wang, Chiuhui Mary, Monaco, Lucia, Filocamo, Mirella
Publicado no Orphanet J Rare Dis (2016)

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Por Healy, Daniel G, Falchi, Mario, O'Sullivan, Sean S, Bonifati, Vincenzo, Durr, Alexandra, Bressman, Susan, Brice, Alexis, Aasly, Jan, Zabetian, Cyrus P, Goldwurm, Stefano, Ferreira, Joaquim J, Tolosa, Eduardo, Kay, Denise M, Klein, Christine, Williams, David R, Marras, Connie, Lang, Anthony E, Wszolek, Zbigniew K, Berciano, Jose, Schapira, Anthony HV, Lynch, Timothy, Bhatia, Kailash P, Gasser, Thomas, Lees, Andrew J, Wood, Nicholas W
Publicado em 2008

Alpha-synuclein REP1 variants and survival in Parkinson’s disease

Por Chung, Sun Ju, Biernacka, Joanna M., Armasu, Sebastian M., Anderson, Kari, Frigerio, Roberta, Aasly, Jan O., Annesi, Grazia, Bentivoglio, Anna Rita, Brighina, Laura, Chartier-Harlin, Marie-Christine, Goldwurm, Stefano, Hadjigeorgiou, Georgios, Jasinska-Myga, Barbara, Jeon, Beom Seok, Kim, Yun Joong, Krüger, Rejko, Lesage, Suzanne, Markopoulou, Katerina, Mellick, George, Morrison, Karen E., Puschmann, Andreas, Tan, Eng-King, Theuns, Jessie, Wirdefeldt, Karin, Wszolek, Zbigniew K., Elbaz, Alexis, Maraganore, Demetrius M.
Publicado em 2014

Single-Cell Expression Profiling of Dopaminergic Neurons Combined with Association Analysis Identifies Pyridoxal Kinase as Parkinson’s Disease Gene

Por Elstner, Matthias, Morris, Christopher M., Heim, Katharina, Lichtner, Peter, Bender, Andreas, Mehta, Divya, Schulte, Claudia, Sharma, Manu, Hudson, Gavin, Goldwurm, Stefano, Giovanetti, Alessandro, Zeviani, Massimo, Burn, David J., McKeith, Ian G., Perry, Robert H., Jaros, E., Krüger, Rejko, Wichmann, H.-Erich, Schreiber, Stefan, Campbell, Harry, Wilson, James F., Wright, Alan F., Dunlop, Malcolm, Pistis, Giorgio, Toniolo, Daniela, Chinnery, Patrick F., Gasser, Thomas, Klopstock, Thomas, Meitinger, Thomas, Prokisch, Holger, Turnbull, Douglass M.
Publicado em 2009

The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases

Por Mora, Marina, Angelini, Corrado, Bignami, Fabrizia, Bodin, Anne-Mary, Crimi, Marco, Di Donato, Jeanne- Hélène, Felice, Alex, Jaeger, Cécile, Karcagi, Veronika, LeCam, Yann, Lynn, Stephen, Meznaric, Marija, Moggio, Maurizio, Monaco, Lucia, Politano, Luisa, de la Paz, Manuel Posada, Saker, Safaa, Schneiderat, Peter, Ensini, Monica, Garavaglia, Barbara, Gurwitz, David, Johnson, Diana, Muntoni, Francesco, Puymirat, Jack, Reza, Mojgan, Voit, Thomas, Baldo, Chiara, Bricarelli, Franca Dagna, Goldwurm, Stefano, Merla, Giuseppe, Pegoraro, Elena, Renieri, Alessandra, Zatloukal, Kurt, Filocamo, Mirella, Lochmüller, Hanns
Publicado no Eur J Hum Genet (2015)