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Transcriptome analysis in LRRK2 and idiopathic Parkinson’s disease at different glucose levels.
Published in:
NPJ Parkinson's Disease, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41531-021-00255-x
By:
- Fernández-Santiago, Rubén;
- Esteve-Codina, Anna;
- Fernández, Manel;
- Valldeoriola, Francesc;
- Sanchez-Gómez, Almudena;
- Muñoz, Esteban;
- Compta, Yaroslau;
- Tolosa, Eduardo;
- Ezquerra, Mario;
- Martí, María J.
Publication type:
Article
Alcohol consumption and lung cancer risk in never smokers: a pooled analysis of case-control studies.
Published in:
European Journal of Public Health, 2018, v. 28, n. 3, p. 521, doi. 10.1093/eurpub/ckx196
By:
- García Lavandeira, José A.;
- Ruano-Ravina, Alberto;
- Kelsey, Karl T.;
- Torres-Durán, María;
- Parente-Lamelas, Isaura;
- Leiro-Fernandez, Virginia;
- Zapata, Maruxa;
- Abal-Arca, Jose;
- Vidal-García, Iria;
- Montero-Martínez, Carmen;
- Amenedo, Margarita;
- Castro-Anón, Olalla;
- Golpe-Gomez, Antonio;
- Guzman-Taveras, Rosirys;
- Martínez, Cristina;
- Provencio, Mariano;
- Mejuto-Martí, María J.;
- García-García, Silvia;
- Fernandez-Villar, Alberto;
- Piíñeiro, María
Publication type:
Article
Upper-limb dystonia secondary to a midbrain hemorrhage.
Published in:
Movement Disorders, 1996, v. 11, n. 1, p. 96, doi. 10.1002/mds.870110119
By:
- Muñoz, J. Esteban;
- Tolosa, Eduardo;
- Saiz, Albert;
- Vila, Nicolás;
- Martí, María J.;
- Blesa, Rafael
Publication type:
Article
Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies.
Published in:
2022
By:
- Pérez‐Oliveira, Sergio;
- Álvarez, Ignacio;
- Rosas, Irene;
- Menendez‐González, Manuel;
- Blázquez‐Estrada, Marta;
- Aguilar, Miquel;
- Corte, Daniela;
- Buongiorno, Mariateresa;
- Molina‐Porcel, Laura;
- Aldecoa, Iban;
- Martí, María J.;
- Sánchez‐Juan, Pascual;
- Infante, Jon;
- González‐Aramburu, Isabel;
- García‐González, Pablo;
- Rosende‐Roca, Maitée;
- Boada, Mercè;
- Ruiz, Agustín;
- Periñán, María Teresa;
- Macías‐García, Daniel
Publication type:
journal article
LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.
Published in:
Movement Disorders, 2012, v. 27, n. 1, p. 146, doi. 10.1002/mds.23968
By:
- Lorenzo-Betancor, Oswaldo;
- Samaranch, Lluís;
- Ezquerra, Mario;
- Tolosa, Eduardo;
- Lorenzo, Elena;
- Irigoyen, Jaione;
- Gaig, Carles;
- Pastor, María A.;
- Soto-Ortolaza, Alexandra I.;
- Ross, Owen A.;
- Rodríguez-Oroz, María C.;
- Valldeoriola, Francesc;
- Martí, María J.;
- Luquin, María R.;
- Perez-Tur, Jordi;
- Burguera, Juan A.;
- Obeso, José A.;
- Pastor, Pau
Publication type:
Article
Cerebrospinal tau, phospho-tau, and beta-amyloid and neuropsychological functions in Parkinson's disease.
Published in:
Movement Disorders, 2009, v. 24, n. 15, p. 2203, doi. 10.1002/mds.22594
By:
- Compta, Yaroslau;
- Martí, María J.;
- Ibarretxe-Bilbao, Naroa;
- Junqué, Carme;
- Valldeoriola, Francesc;
- Muñoz, Esteban;
- Ezquerra, Mario;
- Ríos, Jose;
- Tolosa, Eduardo
Publication type:
Article
Pure akinesia: An unusual phenotype of Hallervorden-Spatz syndrome(A videotape accompanies this article.).
Published in:
Movement Disorders, 2003, v. 18, n. 11, p. 1351, doi. 10.1002/mds.10520
By:
- José L. Molinuevo;
- María J. Martí;
- Rafael Blesa;
- Eduardo Tolosa
Publication type:
Article

Found: 7

Transcriptome analysis in LRRK2 and idiopathic Parkinson’s disease at different glucose levels.

Alcohol consumption and lung cancer risk in never smokers: a pooled analysis of case-control studies.

Upper-limb dystonia secondary to a midbrain hemorrhage.

Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies.

LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation.

Cerebrospinal tau, phospho-tau, and beta-amyloid and neuropsychological functions in Parkinson's disease.

Pure akinesia: An unusual phenotype of Hallervorden-Spatz syndrome(A videotape accompanies this article.).