de Yébenes JG - Search Results

1

Ampuero I, Alegre-Abarrategui J, Rodal I, España A, Ros R, Sendón JL, Galloway EG, Cervelló A, Caminero AB, Zabala A, Erro E, Jarauta F, Morlán L, López-Valdés E, Aladro Y, Seijo M, Rivas GG, Muñoz DG, de Yébenes JG. Ampuero I, et al. Among authors: de yebenes jg. J Alzheimers Dis. 2009;17(4):787-94. doi: 10.3233/JAD-2009-1112. J Alzheimers Dis. 2009. PMID: 19542611

2

Progressive nonfluent aphasia associated with a new mutation V363I in tau gene.

Munoz DG, Ros R, Fatas M, Bermejo F, de Yebenes JG. Munoz DG, et al. Among authors: de yebenes jg. Am J Alzheimers Dis Other Demen. 2007 Aug-Sep;22(4):294-9. doi: 10.1177/1533317507302320. Am J Alzheimers Dis Other Demen. 2007. PMID: 17712160 Free PMC article.

3

A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.

Ros R, Thobois S, Streichenberger N, Kopp N, Sánchez MP, Pérez M, Hoenicka J, Avila J, Honnorat J, de Yébenes JG. Ros R, et al. Among authors: de yebenes jg. Arch Neurol. 2005 Sep;62(9):1444-50. doi: 10.1001/archneur.62.9.1444. Arch Neurol. 2005. PMID: 16157753 Free article.

4

Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1.

Ros R, Gómez Garre P, Hirano M, Tai YF, Ampuero I, Vidal L, Rojo A, Fontan A, Vazquez A, Fanjul S, Hernandez J, Cantarero S, Hoenicka J, Jones A, Ahsan RL, Pavese N, Piccini P, Brooks DJ, Perez-Tur J, Nyggard T, de Yébenes JG. Ros R, et al. Among authors: de yebenes jg. Ann Neurol. 2005 May;57(5):634-41. doi: 10.1002/ana.20449. Ann Neurol. 2005. PMID: 15852377

5

Molecular findings in familial Parkinson disease in Spain.

Hoenicka J, Vidal L, Morales B, Ampuero I, Jiménez-Jiménez FJ, Berciano J, del Ser T, Jiménez A, Ruíz PG, de Yébenes JG. Hoenicka J, et al. Among authors: de yebenes jg. Arch Neurol. 2002 Jun;59(6):966-70. doi: 10.1001/archneur.59.6.966. Arch Neurol. 2002. PMID: 12056932

6

Revisiting genotype-phenotype overlap in neurogenetics: triplet-repeat expansions mimicking spastic paraplegias.

Bettencourt C, Quintáns B, Ros R, Ampuero I, Yáñez Z, Pascual SI, de Yébenes JG, Sobrido MJ. Bettencourt C, et al. Among authors: de yebenes jg. Hum Mutat. 2012 Sep;33(9):1315-23. doi: 10.1002/humu.22148. Epub 2012 Jul 16. Hum Mutat. 2012. PMID: 22753388 Review.

7

The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia.

Zarranz JJ, Alegre J, Gómez-Esteban JC, Lezcano E, Ros R, Ampuero I, Vidal L, Hoenicka J, Rodriguez O, Atarés B, Llorens V, Gomez Tortosa E, del Ser T, Muñoz DG, de Yebenes JG. Zarranz JJ, et al. Among authors: de yebenes jg. Ann Neurol. 2004 Feb;55(2):164-73. doi: 10.1002/ana.10795. Ann Neurol. 2004. PMID: 14755719

8

Parkin deletion causes cerebral and systemic amyloidosis in human mutated tau over-expressing mice.

Rodríguez-Navarro JA, Gómez A, Rodal I, Perucho J, Martinez A, Furió V, Ampuero I, Casarejos MJ, Solano RM, de Yébenes JG, Mena MA. Rodríguez-Navarro JA, et al. Among authors: de yebenes jg. Hum Mol Genet. 2008 Oct 15;17(20):3128-43. doi: 10.1093/hmg/ddn210. Epub 2008 Jul 17. Hum Mol Genet. 2008. PMID: 18640988

9

On the pathogenesis and neuroprotective treatment of Parkinson disease: what have we learned from the genetic forms of this disease?

Mena MA, Rodriguez-Navarro JA, Ros R, de Yebenes JG. Mena MA, et al. Among authors: de yebenes jg. Curr Med Chem. 2008;15(23):2305-20. doi: 10.2174/092986708785909148. Curr Med Chem. 2008. PMID: 18855661 Review.

10

Progressive supranuclear palsy and tau hyperphosphorylation in a patient with a C212Y parkin mutation.

Sánchez MP, Gonzalo I, Avila J, De Yébenes JG. Sánchez MP, et al. Among authors: de yebenes jg. J Alzheimers Dis. 2002 Oct;4(5):399-404. doi: 10.3233/jad-2002-4506. J Alzheimers Dis. 2002. PMID: 12446971

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