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Elvira Valeria De Marco
Researcher at National Research Council
Publications - 26
Citations - 2909
Elvira Valeria De Marco is an academic researcher from National Research Council. The author has contributed to research in topics: Parkinsonism & Single-nucleotide polymorphism. The author has an hindex of 17, co-authored 26 publications receiving 2514 citations. Previous affiliations of Elvira Valeria De Marco include University of Catania.
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Journal ArticleDOI
Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
Ellen Sidransky,Mike A. Nalls,Jan O. Aasly,Judith Aharon-Peretz,Grazia Annesi,Egberto Reis Barbosa,Anat Bar-Shira,Daniela Berg,Jose Bras,Jose Bras,Alexis Brice,Alexis Brice,Chiung-Mei Chen,Lorraine N. Clark,Christel Condroyer,Elvira Valeria De Marco,Alexandra Durr,Alexandra Durr,Michael J. Eblan,Stanley Fahn,Matthew J. Farrer,Hon-Chung Fung,Ziv Gan-Or,Thomas Gasser,Ruth Gershoni-Baruch,Ruth Gershoni-Baruch,Nir Giladi,Nir Giladi,Alida Griffith,Tanya Gurevich,Tanya Gurevich,Cristina Januário,Peter Kropp,Anthony E. Lang,Guey Jen Lee-Chen,Suzanne Lesage,Karen Marder,Ignacio F. Mata,Anat Mirelman,Jun Mitsui,Ikuko Mizuta,Giuseppe Nicoletti,Giuseppe Nicoletti,Catarina R. Oliveira,Ruth Ottman,Avi Orr-Urtreger,Lygia da Veiga Pereira,Aldo Quattrone,Aldo Quattrone,Ekaterina Rogaeva,Arndt Rolfs,Hanna Rosenbaum,Roberto Rozenberg,Ali Samii,Ali Samii,Ali Samii,Ted Samaddar,Claudia Schulte,Manu Sharma,Manu Sharma,Andrew B. Singleton,Andrew B. Singleton,Mariana Spitz,Mariana Spitz,Eng-King Tan,Eng-King Tan,Nahid Tayebi,Tatsushi Toda,André R. Troiano,Shoji Tsuji,Matthias Wittstock,Tyra G. Wolfsberg,Yih-Ru Wu,Cyrus P. Zabetian,Yi Zhao,Shira G. Ziegler +75 more
TL;DR: Data collected demonstrate that there is a strong association between GBA mutations and Parkinson's disease, and those with a GBA mutation presented earlier with the disease, were more likely to have affected relatives, and were morelikely to have atypical clinical manifestations.
Journal ArticleDOI
A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies
Mike A. Nalls,Raquel Duran,Grisel Lopez,Marzena Kurzawa-Akanbi,Ian G. McKeith,Patrick F. Chinnery,Christopher Morris,Jessie Theuns,Jessie Theuns,David Crosiers,David Crosiers,Patrick Cras,Sebastiaan Engelborghs,Peter Paul De Deyn,Christine Van Broeckhoven,Christine Van Broeckhoven,David M. A. Mann,Julie S. Snowden,Stuart Pickering-Brown,Nicola Halliwell,Yvonne S Davidson,Linda Gibbons,Jenny Harris,Una-Marie Sheerin,Jose Bras,John Hardy,Lorraine N. Clark,Karen Marder,Lawrence S. Honig,Daniela Berg,Walter Maetzler,Kathrin Brockmann,Thomas Gasser,Fabiana Novellino,Aldo Quattrone,Grazia Annesi,Elvira Valeria De Marco,Ekaterina Rogaeva,Mario Masellis,Mario Masellis,Sandra E. Black,Sandra E. Black,Juan M. Bilbao,Tatiana Foroud,Bernardino Ghetti,William C. Nichols,Nathan Pankratz,Glenda M. Halliday,Suzanne Lesage,Suzanne Lesage,Suzanne Lesage,Stephan Klebe,Alexandra Durr,Charles Duyckaerts,Charles Duyckaerts,Charles Duyckaerts,Alexis Brice,Benoit I. Giasson,John Q. Trojanowski,Howard I. Hurtig,Nahid Tayebi,Claudia Landazabal,Claudia Landazabal,Melanie A. Knight,Margaux F. Keller,Margaux F. Keller,Andrew B. Singleton,Tyra G. Wolfsberg,Ellen Sidransky +68 more
TL;DR: In this paper, the authors found a significant association between GBA1 mutation carrier status and DLB, with an odds ratio of 8.28 (95% CI, 4.78-14.88).
Journal ArticleDOI
Sex differences in clinical and genetic determinants of levodopa peak-dose dyskinesias in Parkinson disease: an exploratory study.
Mario Zappia,Grazia Annesi,Giuseppe Nicoletti,Gennarina Arabia,Ferdinanda Annesi,Demetrio Messina,Pierfrancesco Pugliese,Patrizia Spadafora,Patrizia Tarantino,Sara Carrideo,Donatella Civitelli,Elvira Valeria De Marco,Innocenza C. Cirò-Candiano,Antonio Gambardella,Aldo Quattrone +14 more
TL;DR: Risk factors for PDD, both clinical and genetic, act in different ways for men and women, and a female sex-related effect for the risk of PDD may be so strong that it overcomes any protective effect due to genetic factors.
Sex Differences in Clinical and Genetic Determinants of Levodopa Peak-Dose Dyskinesias in Parkinson Disease
Mario Zappia,Grazia Annesi,Giuseppe Nicoletti,Gennarina Arabia,Ferdinanda Annesi,Demetrio Messina,Pierfrancesco Pugliese,Patrizia Spadafora,Patrizia Tarantino,Sara Carrideo,Donatella Civitelli,Elvira Valeria De Marco,Innocenza C. Cirò-Candiano,Antonio Gambardella,Aldo Quattrone +14 more
TL;DR: In this article, the CA dinucleotide short tandem repeat (CAn-STR) polymorphism located in the dopamine receptor D2 gene (DRD2) was found to have a strong effect on the appearance of PDD when the multivariate analysis was performed in men.
Journal ArticleDOI
Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
Elvira Valeria De Marco,Grazia Annesi,Patrizia Tarantino,Francesca E. Rocca,Giovanni Provenzano,Donatella Civitelli,Innocenza Claudia Cirò Candiano,Ferdinanda Annesi,Sara Carrideo,Francesca Condino,Giuseppe Nicoletti,Demetrio Messina,Fabiana Novellino,Maurizio Morelli,Aldo Quattrone +14 more
TL;DR: It is suggested that Italian carriers of a GBA mutation have an increased risk of developing Parkinson's disease.