OpenURL Connection Search

Select item for more details and to access through your institution.

α-Synuclein Levels in Blood Plasma from LRRK2 Mutation Carriers.
Published in:
PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052312
By:
- Gorostidi, Ana;
- Bergareche, Alberto;
- Ruiz-Martínez, Javier;
- Martí-Massó, José F.;
- Cruz, María;
- Varghese, Shiji;
- Qureshi, Mohamed M.;
- Alzahmi, Fatimah;
- Al-Hayani, Abdulmonem;
- de Munáin, Adolfo López;
- El-Agnaf, Omar M. A.
Publication type:
Article
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 9, p. 1119, doi. 10.1093/hmg/11.9.1119
By:
- Morante-Redolat, José M.;
- Gorostidi-Pagola, Ana;
- Piquer-Sirerol, Salomé;
- Sáenz, Amets;
- Poza, Juan J.;
- Galán, Juan;
- Gesk, Stefan;
- Sarafidou, Theologia;
- Mautner, Victor-F.;
- Binelli, Simona;
- Staub, Eike;
- Hinzmann, Bernd;
- French, Lisa;
- Prud'homme, Jean-F.;
- Passarelli, Daniela;
- Scannapieco, Paolo;
- Tassinari, Carlo A.;
- Avanzini, Giuliano;
- Martí-Massó, José F.;
- Kluwe, Lan
Publication type:
Article
Tau/α-synuclein ratio and inflammatory proteins in Parkinson's disease: An exploratory study.
Published in:
2017
By:
- Delgado‐Alvarado, Manuel;
- Gago, Belén;
- Gorostidi, Ana;
- Jiménez‐Urbieta, Haritz;
- Dacosta‐Aguayo, Rosalía;
- Navalpotro‐Gómez, Irene;
- Ruiz‐Martínez, Javier;
- Bergareche, Alberto;
- Martí‐Massó, José F.;
- Martínez‐Lage, Pablo;
- Izagirre, Andrea;
- Rodríguez‐Oroz, María C.
Publication type:
journal article
Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2.
Published in:
Movement Disorders, 2014, v. 29, n. 6, p. 750, doi. 10.1002/mds.25778
By:
- Ruiz‐Martínez, Javier;
- de la Riva, Patricia;
- Rodríguez‐Oroz, Maria C.;
- Mondragón Rezola, Elisabet;
- Bergareche, Alberto;
- Gorostidi, Ana;
- Gago, Belen;
- Estanga, Ainara;
- Larrañaga, Nerea;
- Sarasqueta, Cristina;
- López de Munain, Adolfo;
- Martí Massó, José F.
Publication type:
Article
Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations.
Published in:
2011
By:
- Ruiz-Martínez J;
- Gorostidi A;
- Goyenechea E;
- Alzualde A;
- Poza JJ;
- Rodríguez F;
- Bergareche A;
- Moreno F;
- López de Munain A;
- Martí Massó JF;
- Ruiz-Martínez, Javier;
- Gorostidi, Ana;
- Goyenechea, Estibaliz;
- Alzualde, Ainhoa;
- Poza, Juan José;
- Rodríguez, Francisco;
- Bergareche, Alberto;
- Moreno, Fermín;
- López de Munain, Adolfo;
- Martí Massó, José F
Publication type:
journal article
Olfactory deficits and cardiac <sup>123</sup>I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations.
Published in:
Movement Disorders, 2011, v. 26, n. 11, p. 2026, doi. 10.1002/mds.23773
By:
- Ruiz-Martínez, Javier;
- Gorostidi, Ana;
- Goyenechea, Estibaliz;
- Alzualde, Ainhoa;
- Poza, Juan José;
- Rodríguez, Francisco;
- Bergareche, Alberto;
- Moreno, Fermín;
- López de Munain, Adolfo;
- Martí Massó, José F.
Publication type:
Article
Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain).
Published in:
Movement Disorders, 2010, v. 25, n. 14, p. 2340, doi. 10.1002/mds.23278
By:
- Ruiz-Martínez, Javier;
- Gorostidi, Ana;
- Ibañez, Berta;
- Alzualde, Ainhoa;
- Otaegui, David;
- Moreno, Fermin;
- de Munain, Adolfo López;
- Bergareche, Alberto;
- Gómez-Esteban, Juan Carlos;
- Massó, José F. Martí
Publication type:
Article
Identification of a novel THAP1 mutation at R29 amino-acid residue in sporadic patients with early-onset dystonia.
Published in:
Movement Disorders, 2009, v. 24, n. 16, p. 2428, doi. 10.1002/mds.22849
By:
- Paisán-Ruiz, Coro;
- Ruiz-Martinez, Javier;
- Ruibal, Marta;
- Mok, Kin Y.;
- Indakoetxea, Begona;
- Gorostidi, Ana;
- Massó, José F. Martí
Publication type:
Article
Cinnarizine-induced parkinsonism: Ten years later.
Published in:
Movement Disorders, 1998, v. 13, n. 3, p. 453, doi. 10.1002/mds.870130313
By:
- Martí-Massó, José F.;
- Poza, Juan J.
Publication type:
Article
The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics.
Published in:
PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0178093
By:
- Moreno, Fermin;
- Indakoetxea, Begoña;
- Barandiaran, Myriam;
- Caballero, María Cristina;
- Gorostidi, Ana;
- Calafell, Francesc;
- Gabilondo, Alazne;
- Tainta, Mikel;
- Zulaica, Miren;
- Martí Massó, José F.;
- López de Munain, Adolfo;
- Sánchez-Juan, Pascual;
- Lee, Suzee E.
Publication type:
Article

Found: 10