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Results: 1 to 20 of 30

1.

SORT1 Mutation Resulting in Sortilin Deficiency and p75NTR Upregulation in a Family With Essential Tremor.

Sánchez E, Bergareche A, Krebs CE, Gorostidi A, Makarov V, Ruiz-Martinez J, Chorny A, Lopez de Munain A, Marti-Masso JF, Paisán-Ruiz C.

ASN Neuro. 2015 Aug 21;7(4). pii: 1759091415598290. doi: 10.1177/1759091415598290. Print 2015 Jul.

2.

Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2.

Estanga A, Rodriguez-Oroz MC, Ruiz-Martinez J, Barandiaran M, Gorostidi A, Bergareche A, Mondragon E, Lopez de Munain A, Marti-Masso JF.

Parkinsonism Relat Disord. 2014 Oct;20(10):1097-100. doi: 10.1016/j.parkreldis.2014.07.005. Epub 2014 Jul 30.

PMID:
25127457
3.

Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2.

Ruiz-Martínez J, de la Riva P, Rodríguez-Oroz MC, Mondragón Rezola E, Bergareche A, Gorostidi A, Gago B, Estanga A, Larrañaga N, Sarasqueta C, López de Munain A, Martí Massó JF.

Mov Disord. 2014 May;29(6):750-5. doi: 10.1002/mds.25778. Epub 2013 Dec 19.

PMID:
24357540
4.

Lewy bodies under atomic force microscope.

Tercjak A, Bergareche A, Caballero C, Tuñon T, Linazasoro G.

Ultrastruct Pathol. 2014 Feb;38(1):1-5. doi: 10.3109/01913123.2013.825689. Epub 2013 Oct 17.

PMID:
24134525
5.

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

Martí-Massó JF, Bergareche A, Makarov V, Ruiz-Martinez J, Gorostidi A, López de Munain A, Poza JJ, Striano P, Buxbaum JD, Paisán-Ruiz C.

J Mol Med (Berl). 2013 Dec;91(12):1399-406. doi: 10.1007/s00109-013-1075-4. Epub 2013 Aug 20.

6.

Αlpha-synuclein levels in blood plasma from LRRK2 mutation carriers.

Gorostidi A, Bergareche A, Ruiz-Martínez J, Martí-Massó JF, Cruz M, Varghese S, Qureshi MM, Alzahmi F, Al-Hayani A, López de Munáin A, El-Agnaf OM.

PLoS One. 2012;7(12):e52312. doi: 10.1371/journal.pone.0052312. Epub 2012 Dec 27.

7.

Medical, environmental and personal factors of disability in the elderly in Spain: a screening survey based on the International Classification of Functioning.

Virués-Ortega J, de Pedro-Cuesta J, del Barrio JL, Almazan-Isla J, Bergareche A, Bermejo-Pareja F, Fernández-Mayoralas G, García FJ, Garre-Olmo J, Gascon-Bayarri J, Mahillo I, Martínez-Martín P, Mateos R, Rodríguez F, Rojo-Pérez F, Avellanal F, Saz P, Seijo-Martínez M; Spanish Epidemiological Study Group on Aging.

Gac Sanit. 2011 Dec;25 Suppl 2:29-38. doi: 10.1016/j.gaceta.2011.07.021. Epub 2011 Nov 15.

8.

Sleep disorders in Parkinson disease.

Iranzo de Riquer A, Bergareche A, Campos V.

Neurologist. 2011 Nov;17(6 Suppl 1):S38-42. doi: 10.1097/NRL.0b013e31823966f8. Review.

PMID:
22045324
9.

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

Marti-Masso JF, Ruiz-Martínez J, Makarov V, López de Munain A, Gorostidi A, Bergareche A, Yoon S, Buxbaum JD, Paisán-Ruiz C.

Hum Genet. 2012 Mar;131(3):435-42. doi: 10.1007/s00439-011-1086-6. Epub 2011 Sep 13.

PMID:
21912879
10.

Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations.

Ruiz-Martínez J, Gorostidi A, Goyenechea E, Alzualde A, Poza JJ, Rodríguez F, Bergareche A, Moreno F, López de Munain A, Martí Massó JF.

Mov Disord. 2011 Sep;26(11):2026-31. doi: 10.1002/mds.23773. Epub 2011 May 24.

PMID:
21611983
11.

Prevalence of disability in a composite ≥75 year-old population in Spain: a screening survey based on the International Classification of Functioning.

Virués-Ortega J, de Pedro-Cuesta J, Seijo-Martínez M, Saz P, Sánchez-Sánchez F, Rojo-Pérez F, Rodríguez F, Mateos R, Martínez-Martín P, Mahillo I, Gascon-Bayarri J, Garre-Olmo J, García FJ, Fernández-Mayoralas G, Bermejo-Pareja F, Bergareche A, Almazan-Isla J, del Barrio JL.

BMC Public Health. 2011 Mar 23;11:176. doi: 10.1186/1471-2458-11-176.

12.

[Parkinsonism induced by sulpiride and veralipride: two different stories].

Martí Massó JF, Ruiz-Martínez J, Bergareche A, López de Munain A.

Med Clin (Barc). 2011 Oct 15;137(10):473-4. doi: 10.1016/j.medcli.2010.09.038. Epub 2011 Feb 4. Spanish. No abstract available.

PMID:
21295788
13.

Penetrance in Parkinson's disease related to the LRRK2 R1441G mutation in the Basque country (Spain).

Ruiz-Martínez J, Gorostidi A, Ibañez B, Alzualde A, Otaegui D, Moreno F, López de Munain A, Bergareche A, Gómez-Esteban JC, Martí Massó JF.

Mov Disord. 2010 Oct 30;25(14):2340-5. doi: 10.1002/mds.23278.

PMID:
20721916
14.

Prevalence and European comparison of dementia in a ≥75-year-old composite population in Spain.

Virués-Ortega J, de Pedro-Cuesta J, Vega S, Seijo-Martínez M, Saz P, Rodríguez F, Rodríguez-Laso A, Reñé R, de Las Heras SP, Mateos R, Martínez-Martín P, Mahillo-Fernández I, López-Pousa S, Lobo A, Reglà JL, Gascón J, García FJ, Fernández-Martínez M, Boix R, Bermejo-Pareja F, Bergareche A, Sánchez-Sánchez F, de Arce A, del Barrio JL; Spanish Epidemiological Studies on Ageing Group.

Acta Neurol Scand. 2011 May;123(5):316-24. doi: 10.1111/j.1600-0404.2010.01398.x.

PMID:
20636450
15.

What contributes to driving ability in Parkinson's disease.

Cubo E, Martinez Martin P, Gonzalez M, Bergareche A, Campos V, Fernández JM, Alvárez M, Bayes A; Elep Group.

Disabil Rehabil. 2010;32(5):374-8. doi: 10.3109/09638280903168507.

PMID:
19958153
16.

"Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation.

Moreno F, Indakoetxea B, Barandiaran M, Alzualde A, Gabilondo A, Estanga A, Ruiz J, Ruibal M, Bergareche A, Martí-Massó JF, López de Munain A.

Neurology. 2009 Oct 27;73(17):1367-74. doi: 10.1212/WNL.0b013e3181bd82a7.

PMID:
19858458
17.

Prevalence of dementia and major dementia subtypes in Spanish populations: a reanalysis of dementia prevalence surveys, 1990-2008.

de Pedro-Cuesta J, Virués-Ortega J, Vega S, Seijo-Martínez M, Saz P, Rodríguez F, Rodríguez-Laso A, Reñé R, de las Heras SP, Mateos R, Martínez-Martín P, Manubens JM, Mahillo-Fernandez I, López-Pousa S, Lobo A, Reglà JL, Gascón J, García FJ, Fernández-Martínez M, Boix R, Bermejo-Pareja F, Bergareche A, Benito-León J, de Arce A, del Barrio JL.

BMC Neurol. 2009 Oct 19;9:55. doi: 10.1186/1471-2377-9-55.

18.

[Tremor: update and controversy].

Ruiz-Martínez J, Arratibel-Echarren I, Gorostidi-Pagola A, Bergareche A, Martí-Massó JF.

Rev Neurol. 2009 Jan 23;48 Suppl 1:S37-41. Review. Spanish.

19.

Wired for autonomy.

da Rocha AC, Bergareche AM.

Am J Bioeth. 2008 May;8(5):23-5; discussion W1-3. doi: 10.1080/15265160802180042. No abstract available.

PMID:
18642192
20.

Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.

López de Munain A, Alzualde A, Gorostidi A, Otaegui D, Ruiz-Martínez J, Indakoetxea B, Ferrer I, Pérez-Tur J, Sáenz A, Bergareche A, Barandiarán M, Poza JJ, Zabalza R, Ruiz I, Urtasun M, Fernández-Manchola I, Olasagasti B, Espinal JB, Olaskoaga J, Ruibal M, Moreno F, Carrera N, Martí Massó JF.

Biol Psychiatry. 2008 May 15;63(10):946-52. Epub 2007 Oct 22.

PMID:
17950702
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