檢索結果 - Stefano Goldwurm

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  1. 1
    Microtubule Destabilization Is Shared by Genetic and Idiopathic Parkinson’s Disease Patient Fibroblasts

    Microtubule Destabilization Is Shared by Genetic and Idiopathic Parkinson’s Disease Patient Fibroblasts 由 Daniele Cartelli, Stefano Goldwurm, Francesca Casagrande, Gianni Pezzoli, Graziella Cappelletti

    出版 2012
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  2. 2
    Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson’s disease

    Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson’s disease 由 Laura Brighina, Chiara Riva, Francesca Bertola, Enrico Saracchi, Silvia Fermi, Stefano Goldwurm, Carlo Ferrarese

    出版 2013
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  3. 3
    Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease

    Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease 由 Corinne Lautier, Stefano Goldwurm, Alexandra Dürr, Barbara Giovannone, William G. Tsiaras, Gianni Pezzoli, Alexis Brice, Robert J. Smith

    出版 2008
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  4. 4
    SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

    SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population 由 Luca Trotta, Ilaria Guella, Giulia Soldà, Francesca Sironi, Silvana Tesei, Margherita Canesi, Gianni Pezzoli, Stefano Goldwurm, Stefano Duga, Rosanna Asselta

    出版 2011
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  5. 5
    Glucocerebrosidase mutations in primary parkinsonism

    Glucocerebrosidase mutations in primary parkinsonism 由 Rosanna Asselta, Valeria Rimoldi, Chiara Siri, Roberto Cilia, Ilaria Guella, Silvana Tesei, Giulia Soldà, Gianni Pezzoli, Stefano Duga, Stefano Goldwurm

    出版 2014
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  6. 6
    GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling

    GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling 由 Barbara Giovannone, William G. Tsiaras, Suzanne de la Monte, J Kłysik, Corinne Lautier, Galina Karashchuk, Stefano Goldwurm, Robert J. Smith

    出版 2009
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  7. 7
    Alpha-Synuclein Expression in the Oligodendrocyte Lineage: an In Vitro and In Vivo Study Using Rodent and Human Models

    Alpha-Synuclein Expression in the Oligodendrocyte Lineage: an In Vitro and In Vivo Study Using Rodent and Human Models 由 Mehdi Djelloul, Staffan Holmqvist, Antonio Boza‐Serrano, Carla Azevedo, Maggie S. Y. Yeung, Stefano Goldwurm, Jonas Frisén, Tomas Deierborg, Laurent Roybon

    出版 2015
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  8. 8
    The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p

    The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p 由 Letizia Straniero, Valeria Rimoldi, Maura Samarani, Stefano Goldwurm, Alessio Di Fonzo, Rejko Krüger, Michela Deleidi, Massimo Aureli, Giulia Soldà, Stefano Duga, Rosanna Asselta

    出版 2017
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  9. 9
    Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases

    Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases 由 Mirella Filocamo, Chiara Baldo, Stefano Goldwurm, Alessandra Renieri, C. Angelini, Maurizio Moggio, Marina Mora, Giuseppe Merla, Luisa Politano, Barbara Garavaglia, Lorena Casareto, Francesca Bricarelli

    出版 2013
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  10. 10
    Cyclin-G-associated kinase modifies -synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study

    Cyclin-G-associated kinase modifies -synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study 由 Alexandra Dumitriu, Christopher D. Pacheco, Jemma B. Wilk, Katherine E. Strathearn, Jeanne C. Latourelle, Stefano Goldwurm, Gianni Pezzoli, Jean‐Christophe Rochet, S Lindquist, Richard H. Myers

    出版 2011
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  11. 11
    LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population

    LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population 由 Roberto Cilia, Chiara Siri, Damiana Rusconi, Roberta Allegra, Andrea Ghiglietti, Giorgio Sacilotto, Michela Zini, Anna Zecchinelli, Rosanna Asselta, Stefano Duga, Anna Maria Paganoni, Gianni Pezzoli, Manuela Seia, Stefano Goldwurm

    出版 2014
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  12. 12
    Genomewide association study for onset age in Parkinson disease

    Genomewide association study for onset age in Parkinson disease 由 Jeanne C. Latourelle, Nathan Pankratz, Alexandra Dumitriu, Jemma B. Wilk, Stefano Goldwurm, Gianni Pezzoli, Claudio Mariani, Anita L. DeStefano, Cheryl Halter, James F. Gusella, William C. Nichols, Richard H. Myers, Tatiana Foroud

    出版 2009
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  13. 13
    Parkin absence accelerates microtubule aging in dopaminergic neurons

    Parkin absence accelerates microtubule aging in dopaminergic neurons 由 Daniele Cartelli, Alida Amadeo, Alessandra Maria Calogero, Francesca Casagrande, Carmelita De Gregorio, M. Gioria, Naoko Kuzumaki, Ilaria Costa, Jenny Sassone, Andrea Ciammola, Nobutaka Hattori, Hideyuki Okano, Stefano Goldwurm, Laurent Roybon, Gianni Pezzoli, Graziella Cappelletti

    出版 2017
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  14. 14
    Creation of a library of induced pluripotent stem cells from Parkinsonian patients

    Creation of a library of induced pluripotent stem cells from Parkinsonian patients 由 Staffan Holmqvist, Šárka Lehtonen, Margarita Chumarina, Katja A. Puttonen, Carla Azevedo, Olga S. Lebedeva, Marika Ruponen, Minna Oksanen, Mehdi Djelloul, Anna Collin, Stefano Goldwurm, Morten Meyer, Maria A. Lagarkova, С. Л. Киселев, Jari Koıstınaho, Laurent Roybon

    出版 2016
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  15. 15
    TNF-α and α-synuclein fibrils differently regulate human astrocyte immune reactivity and impair mitochondrial respiration

    TNF-α and α-synuclein fibrils differently regulate human astrocyte immune reactivity and impair mitochondrial respiration 由 Kaspar Russ, Gabriel Teku, Luc Bousset, Virginie Redeker, Sara Piel, Ekaterina Savchenko, Yuriy Pomeshchik, Jimmy Savistchenko, Tina C. Stummann, Carla Azevedo, Anna Collin, Stefano Goldwurm, Karina Fog, Eskil Elmér, Mauno Vihinen, Ronald Melki, Laurent Roybon

    出版 2021
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  16. 16
    Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians

    Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians 由 Daniele Ghezzi, Cécilia Marelli, Alessandro Achilli, Stefano Goldwurm, Gianni Pezzoli, Paolo Barone, Maria Teresa Pellecchia, Paolo Stanzione, Livia Brusa, Anna Rita Bentivoglio, Ubaldo Bonuccelli, Lucia Petrozzi, Giovanni Abbruzzese, Roberta Marchese, Pietro Cortelli, Daniela Grimaldi, Paolo Martinelli, Carlo Ferrarese, Barbara Garavaglia, Simonetta Sangiorgi, Valério Carelli, Antonio Torroni, Alberto Albanese, Massimo Zeviani

    出版 2005
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  17. 17
    Nonsteroidal <scp>Anti‐inflammatory</scp> Use and <scp><i>LRRK2</i></scp> Parkinson's Disease Penetrance

    Nonsteroidal <scp>Anti‐inflammatory</scp> Use and <scp><i>LRRK2</i></scp> Parkinson's Disease Penetrance 由 Marta San Luciano, Caroline M. Tanner, Cheryl Meng, Connie Marras, Samuel M. Goldman, Anthony E. Lang, Eduardo Tolosa, Birgitt Schüle, J. William Langston, Alexis Brice, Jean‐Christophe Corvol, Stefano Goldwurm, Christine Klein, Simone Brockman, Daniela Berg, Kathrin Brockmann, Joachim J. Ferreira, Mériem Tazir, George D. Mellick, Carolyn M. Sue, Kazuko Hasegawa, Eng King Tan, Susan Bressman, Rachel Saunders‐Pullman

    出版 2020
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  18. 18
    Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

    Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study 由 Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman, Alexis Brice, Jan Aasly, Cyrus P. Zabetian, Stefano Goldwurm, Joaquim J. Ferreira, Eduardo Tolosa, Denise M. Kay, Christine Klein, David R. Williams, Connie Marras, Anthony E. Lang, Zbigniew K. Wszołek, José Berciano, Anthony H.V. Schapira, Timothy Lynch, Kailash P. Bhatia, Thomas Gasser, Andrew J. Lees, Nicholas Wood

    出版 2008
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  19. 19
    Penetrance estimate of <i>LRRK2</i> p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry

    Penetrance estimate of <i>LRRK2</i> p.G2019S mutation in individuals of non‐Ashkenazi Jewish ancestry 由 Annie Lee, Yuanjia Wang, Roy N. Alcalay, Helen Mejia‐Santana, Rachel Saunders‐Pullman, Susan Bressman, Jean‐Christophe Corvol, Alexis Brice, Suzanne Lesage, Graziella Mangone, Eduardo Tolosa, Claustre Pont‐Sunyer, Dolores Vilas, Birgitt Schüle, Farah Kausar, Tatiana Foroud, Daniela Berg, Kathrin Brockmann, Stefano Goldwurm, Chiara Siri, Rosanna Asselta, Javier Ruiz‐Martínez, Elisabet Mondragón, Connie Marras, Taneera Ghate, Nir Giladi, Anat Mirelman, Karen Marder

    出版 2017
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  20. 20
    Frequency of Loss of Function Variants in <i>LRRK2</i> in Parkinson Disease

    Frequency of Loss of Function Variants in <i>LRRK2</i> in Parkinson Disease 由 Cornelis Blauwendraat, Xylena Reed, Demis A. Kia, Ziv Gan‐Or, Suzanne Lesage, Lasse Pihlstrøm, Rita Guerreiro, J. Raphael Gibbs, Marya S. Sabir, Sarah Ahmed, Jinhui Ding, Roy N. Alcalay, Sharon Hassin‐Baer, Alan Pittman, Janet Brooks, Connor Edsall, Dena Hernández, Sun Ju Chung, Stefano Goldwurm, Mathias Toft, Claudia Schulte, José Brás, Nicholas Wood, Alexis Brice, Huw R. Morris, Sonja W. Scholz, Mike A. Nalls, Andrew B. Singleton, Mark Cookson

    出版 2018
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