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Psychiatric symptoms in Parkinson's disease assessed with the SCL-90R self-reported questionnaire.
Published in:
2010
By:
- Siri C;
- Cilia R;
- De Gaspari D;
- Villa F;
- Goldwurm S;
- Marco C;
- Pezzoli G;
- Antonini A;
- Siri, Chiara;
- Cilia, Roberto;
- De Gaspari, Danilo;
- Villa, Federica;
- Goldwurm, Stefano;
- Marco, Catalano;
- Pezzoli, Gianni;
- Antonini, Angelo
Publication type:
journal article
Psychiatric symptoms in Parkinson’s disease assessed with the SCL-90R self-reported questionnaire.
Published in:
Neurological Sciences, 2010, v. 31, n. 1, p. 35, doi. 10.1007/s10072-009-0165-0
By:
- Siri, Chiara;
- Cilia, Roberto;
- De Gaspari, Danilo;
- Villa, Federica;
- Goldwurm, Stefano;
- Marco, Catalano;
- Pezzoli, Gianni;
- Antonini, Angelo
Publication type:
Article
VEGF Haplotypes are Associated with Increased Risk to Progressive Supranuclear Palsy and Corticobasal Syndrome.
Published in:
Journal of Alzheimer's Disease, 2010, v. 21, n. 1, p. 87, doi. 10.3233/JAD-2010-091615
By:
- Borroni, Barbara;
- Del Bo, Roberto;
- Goldwurm, Stefano;
- Archetti, Silvana;
- Bonvicini, Cristian;
- Agosti, Chiara;
- Bigni, Barbara;
- Papetti, Alice;
- Ghezzi, Serena;
- Sacilotto, Giorgio;
- Pezzoli, Gianni;
- Gennarelli, Massimo;
- Bresolin, Nereo;
- Comi, Giacomo Pietro;
- Padovania, Alessandro
Publication type:
Article
The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks.
Published in:
Orphanet Journal of Rare Diseases, 2016, v. 11, p. 1, doi. 10.1186/s13023-016-0527-7
By:
- 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
Publication type:
Article
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases.
Published in:
Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-129
By:
- 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
Publication type:
Article
Telethon Network of Genetic Biobanks: a key service for diagnosis and research on rare diseases.
Published in:
2013
By:
- 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;
- for Telethon Network of Genetic Biobanks Staff;
- Telethon Network of Genetic Biobanks Staff
Publication type:
journal article
Analysis of ferritin genes in Parkinson disease.
Published in:
Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 11, p. 1450, doi. 10.1515/CCLM.2007.307
By:
- Foglieni, Barbara;
- Ferrari, Francesca;
- Goldwurm, Stefano;
- Santambrogio, Paolo;
- Castiglioni, Emanuela;
- Sessa, Maria;
- Volontè, Maria Antonietta;
- Lalli, Stefania;
- Galli, Carlo;
- Xin-Sheng Wang;
- Connor, James;
- Sironi, Francesca;
- Canesi, Margherita;
- Biasiotto, Giorgio;
- Pezzoli, Gianni;
- Levi, Sonia;
- Ferrari, Maurizio;
- Arosio, Paolo;
- Cremonesi, Laura
Publication type:
Article
The LRRK2 Variant E193K Prevents Mitochondrial Fission Upon MPP+ Treatment by Altering LRRK2 Binding to DRP1.
Published in:
Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00064
By:
- Perez Carrion, Maria;
- Pischedda, Francesca;
- Biosa, Alice;
- Russo, Isabella;
- Straniero, Letizia;
- Civiero, Laura;
- Guida, Marianna;
- Gloeckner, Christian J.;
- Ticozzi, Nicola;
- Tiloca, Cinzia;
- Mariani, Claudio;
- Pezzoli, Gianni;
- Duga, Stefano;
- Pichler, Irene;
- Pan, Lifeng;
- Landers, John E.;
- Greggio, Elisa;
- Hess, Michael W.;
- Goldwurm, Stefano;
- Piccoli, Giovanni
Publication type:
Article
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
Published in:
Nature Genetics, 2011, v. 43, n. 7, p. 699, doi. 10.1038/ng.859
By:
- Höglinger, Günter U.;
- Melhem, Nadine M.;
- Dickson, Dennis W.;
- Sleiman, Patrick M. A.;
- Li-San Wang;
- Klei, Lambertus;
- Rademakers, Rosa;
- de Silva, Rohan;
- Litvan, Irene;
- Riley, David E.;
- van Swieten, John C.;
- Heutink, Peter;
- Wszolek, Zbigniew K.;
- Uitti, Ryan J.;
- Vandrovcova, Jana;
- Hurtig, Howard I.;
- Gross, Rachel G.;
- Maetzler, Walter;
- Goldwurm, Stefano;
- Tolosa, Eduardo
Publication type:
Article
Do Tardive Dyskinesia and l-Dopa Induced Dyskinesia Share Common Genetic Risk Factors? An Exploratory Study.
Published in:
Journal of Molecular Neuroscience, 2013, v. 51, n. 2, p. 380, doi. 10.1007/s12031-013-0020-x
By:
- Greenbaum, Lior;
- Goldwurm, Stefano;
- Zozulinsky, Polina;
- Lifschytz, Tzuri;
- Cohen, Oren;
- Yahalom, Gilad;
- Cilia, Roberto;
- Tesei, Silvana;
- Asselta, Rosanna;
- Inzelberg, Rivka;
- Kohn, Yoav;
- Hassin-Baer, Sharon;
- Lerer, Bernard
Publication type:
Article
Microtubule Destabilization Is Shared by Genetic and Idiopathic Parkinson's Disease Patient Fibroblasts.
Published in:
PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037467
By:
- Cartelli, Daniele;
- Goldwurm, Stefano;
- Casagrande, Francesca;
- Pezzoli, Gianni;
- Cappelletti, Graziella
Publication type:
Article
Replication of association between ELAVL4 and Parkinson disease: the GenePD study.
Published in:
Human Genetics, 2008, v. 124, n. 1, p. 95, doi. 10.1007/s00439-008-0526-4
By:
- DeStefano, Anita L.;
- Latourelle, Jeanne;
- Lew, Mark F.;
- Suchowersky, Oksana;
- Klein, Christine;
- Golbe, Lawrence I.;
- Mark, Margery H.;
- Growdon, John H.;
- Wooten, G. Frederick;
- Watts, Ray;
- Guttman, Mark;
- Racette, Brad A.;
- Perlmutter, Joel S.;
- Marlor, Lynn;
- Shill, Holly A.;
- Singer, Carlos;
- Goldwurm, Stefano;
- Pezzoli, Gianni;
- Saint-Hilaire, Marie H.;
- Hendricks, Audrey E.
Publication type:
Article
Cellular alterations identified in pluripotent stem cell-derived midbrain spheroids generated from a female patient with progressive external ophthalmoplegia and parkinsonism who carries a novel variation (p.Q811R) in the POLG1 gene.
Published in:
Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. 1, doi. 10.1186/s40478-019-0863-7
By:
- Chumarina, Margarita;
- Russ, Kaspar;
- Azevedo, Carla;
- Heuer, Andreas;
- Pihl, Maria;
- Collin, Anna;
- Frostner, Eleonor Åsander;
- Elmer, Eskil;
- Hyttel, Poul;
- Cappelletti, Graziella;
- Zini, Michela;
- Goldwurm, Stefano;
- Roybon, Laurent
Publication type:
Article
TARDBP mutations in a cohort of Italian patients with Parkinson’s disease and atypical parkinsonisms.
Published in:
Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.1020948
By:
- Tiloca, Cinzia;
- Goldwurm, Stefano;
- Calcagno, Narghes;
- Verde, Federico;
- Peverelli, Silvia;
- Calini, Daniela;
- Zecchinelli, Anna Lena;
- Sangalli, Davide;
- Ratti, Antonia;
- Pezzoli, Gianni;
- Silani, Vincenzo;
- Ticozzi, Nicola
Publication type:
Article
Mitochondrial DNA haplogroup K is associated with a lower risk of Parkinson's disease in Italians.
Published in:
European Journal of Human Genetics, 2005, v. 13, n. 6, p. 748, doi. 10.1038/sj.ejhg.5201425
By:
- Ghezzi, Daniele;
- Marelli, Cecilia;
- Achilli, Alessandro;
- Goldwurm, Stefano;
- Pezzoli, Gianni;
- Barone, Paolo;
- Pellecchia, Maria Teresa;
- Stanzione, Paolo;
- Brusa, Livia;
- Bentivoglio, Anna Rita;
- Bonuccelli, Ubaldo;
- Petrozzi, Lucia;
- Abbruzzese, Giovanni;
- Marchese, Roberta;
- Cortelli, Pietro;
- Grimaldi, Daniela;
- Martinelli, Paolo;
- Ferrarese, Carlo;
- Garavaglia, Barbara;
- Sangiorgi, Simonetta
Publication type:
Article
Generation of a transcription map distal to HLA-F.
Published in:
European Journal of Human Genetics, 1998, v. 6, n. 5, p. 475, doi. 10.1038/sj.ejhg.5200211
By:
- Goldwurm, Stefano;
- Van der Griend, Benjamin FH;
- Banyer, Joanne L;
- Cullen, Lara M;
- Zournazi, Anna;
- Menzies, Moira L;
- Busfield, Frances;
- Little, Peter FR;
- Jazwinska, Elizabeth C
Publication type:
Article
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.
Published in:
JAMA Neurology, 2018, v. 75, n. 11, p. 1416, doi. 10.1001/jamaneurol.2018.1885
By:
- Blauwendraat, Cornelis;
- Reed, Xylena;
- Kia, Demis A.;
- Gan-Or, Ziv;
- Lesage, Suzanne;
- Pihlstrøm, Lasse;
- Guerreiro, Rita;
- Gibbs, J. Raphael;
- Sabir, Marya;
- Ahmed, Sarah;
- Ding, Jinhui;
- Alcalay, Roy N.;
- Hassin-Baer, Sharon;
- Pittman, Alan M.;
- Brooks, Janet;
- Edsall, Connor;
- Hernandez, Dena G.;
- Chung, Sun Ju;
- Goldwurm, Stefano;
- Toft, Mathias
Publication type:
Article
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
Published in:
2021
By:
- Lai, Dongbing;
- Alipanahi, Babak;
- Fontanillas, Pierre;
- Schwantes‐An, Tae‐Hwi;
- Aasly, Jan;
- Alcalay, Roy N.;
- Beecham, Gary W.;
- Berg, Daniela;
- Bressman, Susan;
- Brice, Alexis;
- Brockman, Kathrin;
- Clark, Lorraine;
- Cookson, Mark;
- Das, Sayantan;
- Van Deerlin, Vivianna;
- Follett, Jordan;
- Farrer, Matthew J.;
- Trinh, Joanne;
- Gasser, Thomas;
- Goldwurm, Stefano
Publication type:
journal article
DNAJC12 and dopa-responsive nonprogressive parkinsonism.
Published in:
2017
By:
- Straniero, Letizia;
- Guella, Ilaria;
- Cilia, Roberto;
- Parkkinen, Laura;
- Rimoldi, Valeria;
- Young, Alexander;
- Asselta, Rosanna;
- Soldà, Giulia;
- Sossi, Vesna;
- Stoessl, A. Jon;
- Priori, Alberto;
- Nishioka, Kenya;
- Hattori, Nobutaka;
- Follett, Jordan;
- Rajput, Alex;
- Blau, Nenad;
- Pezzoli, Gianni;
- Farrer, Matthew J.;
- Goldwurm, Stefano;
- Rajput, Ali H.
Publication type:
journal article
Single-cell expression profiling of dopaminergic neurons combined with association analysis identifies pyridoxal kinase as Parkinson's disease gene.
Published in:
Annals of Neurology, 2009, v. 66, n. 6, p. 792, doi. 10.1002/ana.21780
By:
- 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
Publication type:
Article
Beyond 35 years of Parkinson’s disease: a comprehensive clinical and instrumental assessment.
Published in:
Journal of Neurology, 2018, v. 265, n. 9, p. 1989, doi. 10.1007/s00415-018-8955-z
By:
- Romagnolo, Alberto;
- Fabbri, Margherita;
- Merola, Aristide;
- Montanaro, Elisa;
- Palermo, Sara;
- Martone, Tiziana;
- Seresini, Agostino;
- Goldwurm, Stefano;
- Rizzone, Mario Giorgio;
- Lopiano, Leonardo
Publication type:
Article
Screening LRRK2 gene mutations in patients with Parkinson's disease in Ghana.
Published in:
2012
By:
- Cilia, Roberto;
- Sironi, Francesca;
- Akpalu, Albert;
- Cham, Momodou;
- Sarfo, Fred;
- Brambilla, Tiziana;
- Bonetti, Alba;
- Amboni, Marianna;
- Goldwurm, Stefano;
- Pezzoli, Gianni
Publication type:
Letter
Penetrance of Glucocerebrosidase (GBA) Mutations in Parkinson's Disease: A Kin Cohort Study.
Published in:
Movement Disorders, 2020, v. 35, n. 11, p. 2111, doi. 10.1002/mds.28200
By:
- Balestrino, Roberta;
- Tunesi, Sara;
- Tesei, Silvana;
- Lopiano, Leonardo;
- Zecchinelli, Anna L.;
- Goldwurm, Stefano
Publication type:
Article
Nonsteroidal Anti‐inflammatory Use and LRRK2 Parkinson's Disease Penetrance.
Published in:
Movement Disorders, 2020, v. 35, n. 10, p. 1755, doi. 10.1002/mds.28189
By:
- San Luciano, Marta;
- Tanner, Caroline M.;
- Meng, Cheryl;
- Marras, Connie;
- Goldman, Samuel M.;
- Lang, Anthony E.;
- Tolosa, Eduardo;
- Schüle, Birgitt;
- Langston, J. William;
- Brice, Alexis;
- Corvol, Jean‐Christophe;
- Goldwurm, Stefano;
- Klein, Christine;
- Brockman, Simone;
- Berg, Daniela;
- Brockmann, Kathrin;
- Ferreira, Joachim J.;
- Tazir, Meriem;
- Mellick, George D.;
- Sue, Carolyn M.
Publication type:
Article
Lewy body pathology and typical Parkinson disease in a patient with a heterozygous (R275W) mutation in the Parkin gene ( PARK2).
Published in:
2012
By:
- Ruffmann, Claudio;
- Zini, Michela;
- Goldwurm, Stefano;
- Bramerio, Manuela;
- Spinello, Sonia;
- Rusconi, Damiana;
- Gambacorta, Marcello;
- Tagliavini, Fabrizio;
- Pezzoli, Gianni;
- Giaccone, Giorgio
Publication type:
Letter
A human minisatellite hosts an alternative transcription start site for NPRL3 driving its expression in a repeat number‐dependent manner.
Published in:
Human Mutation, 2020, v. 41, n. 4, p. 807, doi. 10.1002/humu.23974
By:
- Bertuzzi, Maria;
- Tang, Dave;
- Calligaris, Raffaella;
- Vlachouli, Christina;
- Finaurini, Sara;
- Sanges, Remo;
- Goldwurm, Stefano;
- Catalan, Mauro;
- Antonutti, Lucia;
- Manganotti, Paolo;
- Pizzolato, Gilberto;
- Pezzoli, Gianni;
- Persichetti, Francesca;
- Carninci, Piero;
- Gustincich, Stefano
Publication type:
Article
Whole gene deletion and splicing mutations expand the PINK1 genotypic spectrum.
Published in:
Human Mutation, 2007, v. 28, n. 1, p. 98, doi. 10.1002/humu.9472
By:
- Marongiu, Roberta;
- Brancati, Francesco;
- Antonini, Angelo;
- Ialongo, Tamara;
- Ceccarini, Caterina;
- Scarciolla, Oronzo;
- Capalbo, Anna;
- Benti, Riccardo;
- Pezzoli, Gianni;
- Dallapiccola, Bruno;
- Goldwurm, Stefano;
- Valente, Enza Maria
Publication type:
Article
Cyclin-G-associated kinase modifies α-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 8, p. 1478, doi. 10.1093/hmg/ddr026
By:
- 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.
Publication type:
Article
GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling.
Published in:
Human Molecular Genetics, 2009, v. 18, n. 23, p. 4629, doi. 10.1093/hmg/ddp430
By:
- Giovannone, Barbara;
- Tsiaras, William G.;
- de la Monte, Suzanne;
- Klysik, Jan;
- Lautier, Corinne;
- Karashchuk, Galina;
- Goldwurm, Stefano;
- Smith, Robert J.
Publication type:
Article
Analysis of Nucleotide Variations in Genes of Iron Management in Patients of Parkinson's Disease and Other Movement Disorders.
Published in:
Parkinson's Disease (20420080), 2011, p. 1, doi. 10.4061/2011/827693
By:
- Castiglioni, Emanuela;
- Finazzi, Dario;
- Goldwurm, Stefano;
- Pezzoli, Gianni;
- Forni, Gianluca;
- Girelli, Domenico;
- Maccarinelli, Federica;
- Poli, Maura;
- Ferrari, Maurizio;
- Cremonesi, Laura;
- Arosio, Paolo
Publication type:
Article
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis.
Published in:
Neurogenetics, 2007, v. 8, n. 2, p. 103, doi. 10.1007/s10048-006-0072-y
By:
- Grünewald, Anne;
- Breedveld, Guido;
- Lohmann-Hedrich, Katja;
- Rohé, Christan;
- König, Inke;
- Hagenah, Johann;
- Vanacore, Nicola;
- Meco, Giuseppe;
- Antonini, Angelo;
- Goldwurm, Stefano;
- Lesage, Suzanne;
- Dürr, Alexandra;
- Binkofski, Ferdinand;
- Siebner, Hartwig;
- Münchau, Alexander;
- Brice, Alexis;
- Oostra, Ben;
- Klein, Christine;
- Bonifati, Vincenzo
Publication type:
Article
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.
Published in:
2017
By:
- Lee, Annie J.;
- Wang, Yuanjia;
- Alcalay, Roy N.;
- Mejia‐Santana, Helen;
- Saunders‐Pullman, Rachel;
- Bressman, Susan;
- Corvol, Jean‐Christophe;
- Brice, Alexis;
- Lesage, Suzanne;
- Mangone, Graziella;
- Tolosa, Eduardo;
- Pont‐Sunyer, Claustre;
- Vilas, Dolores;
- Schüle, Birgitt;
- Kausar, Farah;
- Foroud, Tatiana;
- Berg, Daniela;
- Brockmann, Kathrin;
- Goldwurm, Stefano;
- Siri, Chiara
Publication type:
journal article
Protein-redistribution diet in a case of tyrosine hydroxylase enzyme deficiency.
Published in:
2017
By:
- Cassani, Erica;
- Barichella, Michela;
- Ferri, Valentina;
- Pusani, Chiara;
- Goldwurm, Stefano;
- Siri, Chiara;
- Zini, Michela;
- Zorzi, Giovanna Simonetta;
- Cereda, Emanuele;
- Iorio, Laura;
- Pinelli, Giovanna;
- Sacilotto, Giorgio;
- Pezzoli, Gianni
Publication type:
Case Study
LRRK2-G2019S mutation is not associated with an increased cancer risk: A kin-cohort study.
Published in:
Movement Disorders, 2014, v. 29, n. 10, p. 1325, doi. 10.1002/mds.25969
By:
- Allegra, Roberta;
- Tunesi, Sara;
- Cilia, Roberto;
- Pezzoli, Gianni;
- Goldwurm, Stefano
Publication type:
Article
Alpha-synuclein repeat variants and survival in Parkinson's disease.
Published in:
Movement Disorders, 2014, v. 29, n. 8, p. 1053, doi. 10.1002/mds.25841
By:
- 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.
Publication type:
Article
The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.
Published in:
Movement Disorders, 2012, v. 27, n. 6, p. 800, doi. 10.1002/mds.24927
By:
- Guella, Ilaria;
- Soldà, Giulia;
- Cilia, Roberto;
- Pezzoli, Gianni;
- Asselta, Rosanna;
- Duga, Stefano;
- Goldwurm, Stefano
Publication type:
Article
Kin-cohort analysis of LRRK2-G2019S penetrance in Parkinson's disease.
Published in:
Movement Disorders, 2011, v. 26, n. 11, p. 2144, doi. 10.1002/mds.23807
By:
- Goldwurm, Stefano;
- Tunesi, Sara;
- Tesei, Silvana;
- Zini, Michela;
- Sironi, Francesca;
- Primignani, Paola;
- Magnani, Corrado;
- Pezzoli, Gianni
Publication type:
Article
Striatal dopamine transporter binding in Parkinson's disease associated with the LRRK2 Gly2019Ser mutation.
Published in:
Movement Disorders, 2006, v. 21, n. 8, p. 1144, doi. 10.1002/mds.20909
By:
- Isaias, Ioannis U.;
- Benti, Riccardo;
- Goldwurm, Stefano;
- Zini, Michela;
- Cilia, Roberto;
- Gerundini, Paolo;
- Di Fonzo, Alessio;
- Bonifati, Vincenzo;
- Pezzoli, Gianni;
- Antonini, Angelo
Publication type:
Article
Genetic, clinical, and imaging characterization of one patient with late-onset, slowly progressive, pantothenate kinase-associated neurodegeneration.
Published in:
Movement Disorders, 2006, v. 21, n. 3, p. 417, doi. 10.1002/mds.20774
By:
- Antonini, Angelo;
- Goldwurm, Stefano;
- Benti, Riccardo;
- Prokisch, Holger;
- Ebhardt, Monika;
- Cilia, Roberto;
- Zini, Michela;
- Righini, Andrea;
- Cossu, Giovanni;
- Pezzoli, Gianni
Publication type:
Article
The Length of SNCA Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's Disease.
Published in:
Frontiers in Neurology, 2018, p. 1, doi. 10.3389/fneur.2018.00213
By:
- Corrado, Lucia;
- De Marchi, Fabiola;
- Tunesi, Sara;
- Oggioni, Gaia Donata;
- Carecchio, Miryam;
- Magistrelli, Luca;
- Tesei, Silvana;
- Riboldazzi, Giulio;
- Di Fonzo, Alessio;
- Locci, Clarissa;
- Trezzi, Ilaria;
- Zangaglia, Roberta;
- Cereda, Cristina;
- D'Alfonso, Sandra;
- Magnani, Corrado;
- Comi, Giacomo P.;
- Bono, Giorgio;
- Pacchetti, Claudio;
- Cantello, Roberto;
- Goldwurm, Stefano
Publication type:
Article

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