Catene di Markov e applicazioni algoritmiche

Por Goldwurm, Massimiliano
Publicado em 2024-01-31

Catene di Markov e applicazioni algoritmiche

Por Goldwurm, Massimiliano
Publicado em 2024-01-31

Haemochromatosis after the discovery of HFE ("HLA-H")

Por GOLDWURM, S, POWELL, L
Publicado em 1997

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

Generation of an induced pluripotent stem cell line (CSC-44) from a Parkinson's disease patient carrying a compound heterozygous mutation (c.823C>T and EX6 del) in the PARK2 gene

Por Ana Marote, Yuriy Pomeshchik, Stefano Goldwurm, Anna Collin, Nuno J. Lamas, Luísa Pinto, António J. Salgado, Laurent Roybon
Publicado em 2018-03-01

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)

Molybdenum(VI) salts convert the xanthine oxidoreductase apoprotein into the active enzyme in mouse L929 fibroblastic cells.

Por Falciani, F, Terao, M, Goldwurm, S, Ronchi, A, Gatti, A, Minoia, C, Li Calzi, M, Salmona, M, Cazzaniga, G, Garattini, E
Publicado em 1994

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

Haplotype analysis in Australian hemochromatosis patients: evidence for a predominant ancestral haplotype exclusively associated with hemochromatosis.

Por Jazwinska, E C, Pyper, W R, Burt, M J, Francis, J L, Goldwurm, S, Webb, S I, Lee, S C, Halliday, J W, Powell, L W
Publicado em 1995

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