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16 results for Marti-Masso,+Jose-Felix

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ArticlesPeer ReviewedFull Text
Inflammatory profile in LRRK2-associated prodromal and clinical PD
Author / Creator:Brockmann, Kathrin ; Apel, Anja ; Schulte, Claudia ; Schneiderhan-Marra, Nicole ; Pont-Sunyer, Claustre ; Vilas, Dolores ; Ruiz-Martinez, Javier ; Langkamp, Markus ; Corvol, Jean-Christophe ; Cormier, Florence ; Knorpp, Thomas ; Joos, Thomas O. ; Gasser, Thomas ; Schüle, Birgitt ; Aasly, Jan O. ; Foroud, Tatiana ; Marti-Masso, Jose Felix ; Brice, Alexis ; Tolosa, Eduardo ; Marras, Connie ; Berg, Daniela ; Maetzler, Walter
Publisher:England: BioMed Central Ltd
Journal title:Journal of neuroinflammation, 2016-05, Vol.13 (1), p.122-122, Article 122
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The long-acting dopamine receptor agonist Cabergoline in early Parkinson's disease: Final results of a 5-year, double-blind, levodopa-controlled study
Author / Creator:BRACCO, Fulvio ; BATTAGLIA, Angelo ; CHOUZA, Carlos ; DUPONT, Erik ; GERSHANIK, Oscar ; MASSO, Jose Felix ; MONTASTRUC, Jean-Louis
Publisher:Hong Kong: Adis International
Journal title:CNS drugs, 2004-01, Vol.18 (11), p.733-746
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Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue
Author / Creator:Devine, Michael J. ; Kaganovich, Alice ; Ryten, Mina ; Mamais, Adamantios ; Trabzuni, Daniah ; Manzoni, Claudia ; McGoldrick, Philip ; Chan, Diane ; Dillman, Allissa ; Zerle, Julia ; Horan, Susannah ; Taanman, Jan-Willem ; Hardy, John ; Marti-Masso, Jose-Felix ; Healey, Daniel ; Schapira, Anthony H. ; Wolozin, Benjamin ; Bandopadhyay, Rina ; Cookson, Mark R. ; van der Brug, Marcel P. ; Lewis, Patrick A.
Publisher:United States: Public Library of Science
Journal title:PloS one, 2011-07, Vol.6 (7), p.e22489-e22489
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Correction: Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue
Author / Creator:Devine, Michael J. ; Kaganovich, Alice ; Ryten, Mina ; Mamais, Adamantios ; Trabzuni, Daniah ; Manzoni, Claudia ; McGoldrick, Philip ; Chan, Diane ; Dillman, Allissa ; Zerle, Julia ; Horan, Susannah ; Taanman, Jan-Willem ; Hardy, John ; Marti-Masso, Jose-Felix ; Healy, Daniel ; Schapira, Anthony H. ; Wolozin, Benjamin ; Bandopadhyay, Rina ; Cookson, Mark R. ; van der Brug, Marcel P. ; Lewis, Patrick A.
Publisher:San Francisco: Public Library of Science
Journal title:PloS one, 2012-01, Vol.7 (1)
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Selection of entropy based features for the analysis of the Archimedes' spiral applied to essential tremor
Author / Creator:López-De-Ipiña, Karmele ; Bergareche, Alberto ; De La Riva, Patricia ; Sole-Casals, Jordi ; Faundez-Zanuy, Marcos ; Jose Felix Marti-Masso ; Iturrate, Mikel ; Beitia, Blanca ; Calvo, Pilar ; Sesa-Nogueras, Enric ; Roure, Josep ; Gurrutxaga, Itziar ; Garcia-Melero, Joseba
Publisher:Ithaca: Cornell University Library, arXiv.org
Journal title:arXiv.org, 2022-03
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The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism
Author / Creator:Martí-Massó, Jose Felix ; Bergareche, Alberto ; Makarov, Vladimir ; Ruiz-Martinez, Javier ; Gorostidi, Ana ; de Munain, Adolfo López ; Poza, Juan Jose ; Striano, Pasquale ; Buxbaum, Joseph D. ; Paisán-Ruiz, Coro
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of molecular medicine (Berlin, Germany), 2013-12, Vol.91 (12), p.1399-1406
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GIGYF2 mutation in late-onset Parkinson’s disease with cognitive impairment
Author / Creator:Ruiz-Martinez, Javier ; Krebs, Catharine E ; Makarov, Vladimir ; Gorostidi, Ana ; Martí-Massó, Jose Félix ; Paisán-Ruiz, Coro
Publisher:England: Nature Publishing Group
Journal title:Journal of human genetics, 2015-10, Vol.60 (10), p.637-640
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Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research
Author / Creator:Wray, Selina ; Self, Matthew ; Lewis, Patrick A. ; Taanman, Jan-Willem ; Ryan, Natalie S. ; Mahoney, Colin J. ; Liang, Yuying ; Devine, Michael J. ; Sheerin, Una-Marie ; Houlden, Henry ; Morris, Huw R. ; Healy, Daniel ; Marti-Masso, Jose-Felix ; Preza, Elisavet ; Barker, Suzanne ; Sutherland, Margaret ; Corriveau, Roderick A. ; D'Andrea, Michael ; Schapira, Anthony H. V. ; Uitti, Ryan J. ; Guttman, Mark ; Opala, Grzegorz ; Jasinska-Myga, Barbara ; Puschmann, Andreas ; Nilsson, Christer ; Espay, Alberto J. ; Slawek, Jaroslaw ; Gutmann, Ludwig ; Boeve, Bradley F. ; Boylan, Kevin ; Stoessl, A. Jon ; Ross, Owen A. ; Maragakis, Nicholas J. ; Van Gerpen, Jay ; Gerstenhaber, Melissa ; Gwinn, Katrina ; Dawson, Ted M. ; Isacson, Ole ; Marder, Karen S. ; Clark, Lorraine N. ; Przedborski, Serge E. ; Finkbeiner, Steven ; Rothstein, Jeffrey D. ; Wszolek, Zbigniew K. ; Rossor, Martin N. ; Hardy, John
Publisher:United States: Public Library of Science
Journal title:PloS one, 2012-08, Vol.7 (8), p.e43099
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Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia
Author / Creator:Marti-Masso, Jose Felix ; Ruiz-Martínez, Javier ; Makarov, Vladimir ; de Munain, Adolfo López ; Gorostidi, Ana ; Bergareche, Alberto ; Yoon, Seungtai ; Buxbaum, Joseph D. ; Paisán-Ruiz, Coro
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Human genetics, 2012-03, Vol.131 (3), p.435-442
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Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants
Author / Creator:Alcalay, Roy N. ; Aasly, Jan ; Berg, Daniela ; Bressman, Susan ; Brice, Alexis ; Brockmann, Kathrin ; Chan, Piu ; Clark, Lorraine ; Cormier, Florence ; Corvol, Jean-Christophe ; Durr, Alexandra ; Facheris, Maurizio ; Farrer, Matthew ; Foroud, Tatiana M. ; Gasser, Thomas ; Giladi, Nir ; Halter, Cheryl ; Lang, Anthony ; Langston, J. William ; Marras, Connie ; Marti-Masso, Jose-Felix ; Ruiz Martinez, Javier ; Mejia-Santana, Helen ; Mirelman, Anat ; Pont-Sunyer, Claustre ; Orr-Urtreger, Avi ; Raymond, Deborah ; Saunders-Pullman, Rachel ; Schüle, Birgitt ; Tanner, Caroline ; Tolosa, Eduardo ; Urkowitz, Alison ; Vilas, Dolores ; Wise, Adina ; Marder, Karen
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2014-08, Vol.16 (8), p.644-645
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Michael J. Fox Foundation Consortium: Geographical Differences in Returning Genetic Research Data to Study Participants
Author / Creator:Alcalay, Roy N. ; Aasly, Jan ; Berg, Daniela ; Bressman, Susan ; Brice, Alexis ; Brockmann, Kathrin ; Chan, Piu ; Clark, Lorraine ; Corvol, Jean-Christophe ; Durr, Alexandra ; Farrer, Matthew ; Foroud, Tatiana M. ; Gasser, Thomas ; Giladi, Nir ; Halter, Cheryl ; Hentati, Fayçal ; Lang, Anthony ; Langston, J. William ; Marder, Karen ; Marras, Connie ; Marti-Masso, Jose-Felix ; Martinez, Javier Ruiz ; Mejia-Santana, Helen ; Mirelman, Anat ; Pont, Claustre ; Orr-Urtreger, Avi ; Raymond, Deborah ; Saunders-Pullman, Rachel ; Schüle, Birgitt ; Tanner, Caroline ; Tolosa, Eduardo ; Vilas, Dolores ; Wise, Adina ; Facheris, Maurizio
Journal title:Genetics in medicine, 2014-08, Vol.16 (8), p.644-645
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ArticlesPeer ReviewedFull Text
The Long-Acting Dopamine Receptor Agonist Cabergoline in Early Parkinson???s Disease: Final Results of a 5-Year, Double-Blind, Levodopa-Controlled Study
Author / Creator:Bracco, Fulvio ; Battaglia, Angelo ; Chouza, Carlos ; Dupont, Erik ; Gershanik, Oscar ; Marti Masso, Jose Felix ; Montastruc, Jean-Louis
Journal title:CNS drugs, 2004, Vol.18 (11), p.733-746
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Analysis of Fine Motor Skills in Essential Tremor: Combining Neuroimaging and Handwriting Biomarkers for Early Management
Author / Creator:Lopez-de-Ipina, Karmele ; Solé-Casals, Jordi ; Sánchez-Méndez, José Ignacio ; Romero-Garcia, Rafael ; Fernandez, Elsa ; Requejo, Catalina ; Poologaindran, Anujan ; Faúndez-Zanuy, Marcos ; Martí-Massó, José Félix ; Bergareche, Alberto ; Suckling, John
Publisher:Lausanne: Frontiers Research Foundation
Journal title:Frontiers in human neuroscience, 2021-06, Vol.15, p.648573-648573
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Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels
Author / Creator:Gorostidi, Ana ; Martí-Massó, José Félix ; Bergareche, Alberto ; Rodríguez-Oroz, Mari Cruz ; López de Munain, Adolfo ; Ruiz-Martínez, Javier
Publisher:Cham: Springer International Publishing
Journal title:Molecular diagnosis & therapy, 2016-10, Vol.20 (5), p.481-491
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Neuropsychological Features of Asymptomatic c.709-1G>A Progranulin Mutation Carriers
Author / Creator:Barandiaran, Myriam ; Estanga, Ainara ; Moreno, Fermín ; Indakoetxea, Begoña ; Alzualde, Ainhoa ; Balluerka, Nekane ; Martí Massó, José Félix ; de Munain, Adolfo López
Publisher:New York, USA: Cambridge University Press
Journal title:Journal of the International Neuropsychological Society, 2012-11, Vol.18 (6), p.1086-1090
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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
Author / Creator:Nalls, Mike A, PhD ; McLean, Cory Y, PhD ; Rick, Jacqueline, PhD ; Eberly, Shirley, MS ; Hutten, Samantha J, PhD ; Gwinn, Katrina, MD ; Sutherland, Margaret, PhD ; Martinez, Maria, PhD ; Heutink, Peter, PhD ; Williams, Nigel M, PhD ; Hardy, John, PhD ; Gasser, Thomas, MD ; Brice, Alexis, MD ; Price, T Ryan, MS ; Nicolas, Aude, PhD ; Keller, Margaux F, PhD ; Molony, Cliona, PhD ; Gibbs, J Raphael, MS ; Chen-Plotkin, Alice, MD ; Suh, Eunran, PhD ; Letson, Christopher, BS ; Fiandaca, Massimo S, MD ; Mapstone, Mark, PhD ; Federoff, Howard J, MD ; Noyce, Alastair J, MRCP ; Morris, Huw, MD ; Van Deerlin, Vivianna M, MD ; Weintraub, Daniel, MD ; Zabetian, Cyrus, MD ; Hernandez, Dena G, MS ; Lesage, Suzanne, PhD ; Mullins, Meghan, BA ; Conley, Emily Drabant, PhD ; Northover, Carrie A M, PhD ; Frasier, Mark, PhD ; Marek, Ken, MD ; Day-Williams, Aaron G, PhD ; Stone, David J, PhD ; Ioannidis, John P A, Prof ; Singleton, Andrew B, Dr
Publisher:England: Elsevier Ltd
Journal title:Lancet neurology, 2015-10, Vol.14 (10), p.1002-1009
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Inflammatory profile in LRRK2-associated prodromal and clinical PD

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The long-acting dopamine receptor agonist Cabergoline in early Parkinson's disease: Final results of a 5-year, double-blind, levodopa-controlled study

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Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue

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Correction: Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue

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Selection of entropy based features for the analysis of the Archimedes' spiral applied to essential tremor

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The ACMSD gene, involved in tryptophan metabolism, is mutated in a family with cortical myoclonus, epilepsy, and parkinsonism

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GIGYF2 mutation in late-onset Parkinson’s disease with cognitive impairment

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Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

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Exome sequencing identifies GCDH (glutaryl-CoA dehydrogenase) mutations as a cause of a progressive form of early-onset generalized dystonia

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Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants

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Michael J. Fox Foundation Consortium: Geographical Differences in Returning Genetic Research Data to Study Participants

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The Long-Acting Dopamine Receptor Agonist Cabergoline in Early Parkinson???s Disease: Final Results of a 5-Year, Double-Blind, Levodopa-Controlled Study

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Analysis of Fine Motor Skills in Essential Tremor: Combining Neuroimaging and Handwriting Biomarkers for Early Management

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Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels

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Neuropsychological Features of Asymptomatic c.709-1G>A Progranulin Mutation Carriers

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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

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