Works by Marti-Masso, Jose Felix

Results: 19

Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques.

Published in:

2006

By:

Simón-Sánchez, Javier;
Martí-Massó, José-Félix;
Sánchez-Mut, José Vicente;
Paisán-Ruiz, Coro;
Martínez-Gil, Angel;
Ruiz-Martínez, Javier;
Sáenz, Amets;
Singleton, Andrew B.;
López de Munain, Adolfo;
Pérez-Tur, Jordi;
Simón-Sánchez, Javier;
Martí-Massó, José-Félix;
Sánchez-Mut, José Vicente;
Paisán-Ruiz, Coro;
Martínez-Gil, Angel;
Ruiz-Martínez, Javier;
Sáenz, Amets;
López de Munain, Adolfo;
Pérez-Tur, Jordi

Publication type:

journal article

Higher Frequency of Certain Cancers in LRRK2 G2019S Mutation Carriers With Parkinson Disease A Pooled Analysis.

Published in:

JAMA Neurology, 2015, v. 72, n. 1, p. 58, doi. 10.1001/jamaneurol.2014.1973

By:

Agalliu, Ilir;
San Luciano, Marta;
Mirelman, Anat;
Giladi, Nir;
Waro, Bjorg;
Aasly, Jan;
Inzelberg, Rivka;
Hassin-Baer, Sharon;
Friedman, Eitan;
Ruiz-Martinez, Javier;
Marti-Masso, Jose Felix;
Orr-Urtreger, Avi;
Bressman, Susan;
Saunders-Pullman, Rachel

Publication type:

Article

DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2 R1441G Parkinson's disease.

Published in:

2016

By:

Bergareche, Alberto;
Rodríguez‐Oroz, Maria Cruz;
Estanga, Ainara;
Gorostidi, Ana;
López de Munain, Adolfo;
Castillo‐Triviño, Tamara;
Ruiz‐Martínez, Javier;
Mondragón, Elisabet;
Gaig, Carles;
Lomeña, Francisco;
Sarasqueta, Cristina;
Tolosa, Eduardo;
Martí‐Massó, José Félix

Publication type:

journal article

Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2.

Published in:

Movement Disorders, 2009, v. 24, n. 13, p. 1998, doi. 10.1002/mds.22677

By:

Martí-Massó, José-Félix;
Ruiz-Martínez, Javier;
Bolaño, Maria J.;
Ruiz, Irune;
Gorostidi, Ana;
Moreno, Fermin;
Ferrer, Isidre;
de Munain, Adolfo López

Publication type:

Article

Tremor dominant parkinsonism: Clinical description and LRRK2 mutation screening.

Published in:

Movement Disorders, 2008, v. 23, n. 4, p. 518, doi. 10.1002/mds.21771

By:

Clarimón, Jordi;
Pagonabarraga, Javier;
Paisán-Ruíz, Coro;
Campolongo, Antonia;
Pascual-Sedano, Berta;
Martí-Massó, José-Félix;
Singleton, Andrew B.;
Kulisevsky, Jaime

Publication type:

Article

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

Published in:

2004

By:

Bracco, Fulvio;
Battaglia, Angelo;
Chouza, Carlos;
Dupont, Erik;
Gershanik, Oscar;
Marti Masso, Jose Felix;
Montastruc, Jean-Louis;
PKDS009 Study Group

Publication type:

journal article

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

Published in:

PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043099

By:

Wray, Selina;
Self, Matthew;
Lewis, Patrick A.;
Taanman, Jan-Willem;
Ryan, Natalie S.;
Mahoney, Colin J.;
Yuying Liang;
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.

Publication type:

Article

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

Published in:

PLoS ONE, 2011, v. 6, n. 7, p. 1, doi. 10.1371/journal.pone.0022489

By:

Devine, Michael J.;
Kaganovich, Alice;
Ryten, Mina;
Mamais, Adamantios;
Trabzuni, Daniah;
Manzoni, Claudia;
McGoldrick, Philip;
Diane Chan;
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.

Publication type:

Article

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

Published in:

Journal of Human Genetics, 2015, v. 60, n. 10, p. 637, doi. 10.1038/jhg.2015.69

By:

Ruiz-Martinez, Javier;
Krebs, Catharine E;
Makarov, Vladimir;
Gorostidi, Ana;
Martí-Massó, Jose Félix;
Paisán-Ruiz, Coro

Publication type:

Article

SCN4A pore mutation pathogenetically contributes to autosomal dominant essential tremor and may increase susceptibility to epilepsy.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 24, p. 7111, doi. 10.1093/hmg/ddv410

By:

Bergareche, Alberto;
Bednarz, Marcin;
Sánchez, Elena;
Krebs, Catharine E.;
Ruiz-Martinez, Javier;
La Riva, Patricia De;
Makarov, Vladimir;
Gorostidi, Ana;
Jurkat-Rott, Karin;
Marti-Masso, Jose Felix;
Paisán-Ruiz, Coro

Publication type:

Article

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

Published in:

Frontiers in Human Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnhum.2021.648573

By:

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

Publication type:

Article

The Discovery of the Dardarin Gene 15 Years Later: A Globalized Local History.

Published in:

2020

By:

López de Munain, Adolfo;
Martí Massó, José Félix;
Pérez Tur, Jordi

Publication type:

Letter

The Discovery of the Dardarin Gene 15 Years Later: A Globalized Local History.

Published in:

Movement Disorders, 2020, v. 35, n. 4, p. 708, doi. 10.1002/mds.27969

By:

López de Munain, Adolfo;
Martí Massó, José Félix;
Pérez Tur, Jordi

Publication type:

Article

Antipsychotic prescribing in older people. Which drug?

Published in:

2004

By:

Martí Massó, José Félix

Publication type:

Letter

Inflammatory profile in LRRK2-associated prodromal and clinical PD.

Published in:

2016

By:

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

Publication type:

journal article

SORT1 Mutation Resulting in Sortilin Deficiency and p75<sup>NTR</sup> Upregulation in a Family With Essential Tremor.

Published in:

ASN Neuro, 2015, v. 7, n. 4, p. 1, doi. 10.1177/1759091415598290

By:

Sánchez, Elena;
Bergareche, Alberto;
Krebs, Catharine E.;
Gorostidi, Ana;
Makarov, Vladimir;
Ruiz-Martinez, Javier;
Chorny, Alejo;
de Munain, Adolfo Lopez;
Marti-Masso, Jose Felix;
Paisán-Ruiz, Coro

Publication type:

Article

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

Published in:

Journal of the International Neuropsychological Society, 2012, v. 18, n. 6, p. 1086, doi. 10.1017/S1355617712000823

By:

Barandiaran, Myriam;
Estanga, Ainara;
Moreno, Fermín;
Indakoetxea, Begoña;
Alzualde, Ainhoa;
Balluerka, Nekane;
Martí Massó, José Félix;
de Munain, Adolfo López

Publication type:

Article

Headache and other complications following intrathecal chemotherapy administration.

Published in:

2017

By:

De la Riva, Patricia;
Andres-Marín, Naiara;
Gonzalo-Yubero, Nora;
Tainta-Cuezva, Mikel;
Caminos, Nerea;
Urtasun-Ocariz, Miguel Ángel;
Martí-Massó, Jose Félix

Publication type:

Letter

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

Published in:

Journal of Molecular Medicine, 2013, v. 91, n. 12, p. 1399, doi. 10.1007/s00109-013-1075-4

By:

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

Publication type:

Article