Publications by authors named "Jon Infante"

100Publications

MicroRNA Deregulation in Blood Serum Identifies Multiple System Atrophy Altered Pathways.

Mov Disord 2020 Oct 20;35(10):1873-1879. Epub 2020 Jul 20.

Lab of Parkinson Disease and Other Neurodegenerative Movement Disorders: Clinical and Experimental Research; Department of Neurology, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Institut de Neurociències, Universitat de Barcelona, Barcelona, Spain.

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http://dx.doi.org/10.1002/mds.28143DOI Listing
October 2020

Social Cognition in Chiari Malformation Type I: a Preliminary Characterization.

Cerebellum 2020 Jun;19(3):392-400

Neurology Service, University Hospital Marqués de Valdecilla, IDIVAL, University of Cantabria, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas-CIBERNED, Santander, Spain.

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http://dx.doi.org/10.1007/s12311-020-01117-7DOI Listing
June 2020

Very early Guillain-Barré syndrome: A clinical-electrophysiological and ultrasonographic study.

Clin Neurophysiol Pract 2020 30;5:1-9. Epub 2019 Nov 30.

Service of Neurology, University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", Santander, Spain.

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http://dx.doi.org/10.1016/j.cnp.2019.11.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6923288PMC
November 2019

Nonpharmacological, nonsurgical treatments for freezing of gait in Parkinson's disease: A systematic review.

Mov Disord 2020 02 26;35(2):204-214. Epub 2019 Nov 26.

Neurology Service, University Hospital Marqués de Valdecilla-IDIVAL, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1002/mds.27913DOI Listing
February 2020

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.

Authors:
Sara Bandres-Ciga Sarah Ahmed Marya S Sabir Cornelis Blauwendraat Astrid D Adarmes-Gómez Inmaculada Bernal-Bernal Marta Bonilla-Toribio Dolores Buiza-Rueda Fátima Carrillo Mario Carrión-Claro Pilar Gómez-Garre Silvia Jesús Miguel A Labrador-Espinosa Daniel Macias Carlota Méndez-Del-Barrio Teresa Periñán-Tocino Cristina Tejera-Parrado Laura Vargas-González Monica Diez-Fairen Ignacio Alvarez Juan Pablo Tartari Mariateresa Buongiorno Miquel Aguilar Ana Gorostidi Jesús Alberto Bergareche Elisabet Mondragon Ana Vinagre-Aragon Ioana Croitoru Javier Ruiz-Martínez Oriol Dols-Icardo Jaime Kulisevsky Juan Marín-Lahoz Javier Pagonabarraga Berta Pascual-Sedano Mario Ezquerra Ana Cámara Yaroslau Compta Manel Fernández Rubén Fernández-Santiago Esteban Muñoz Eduard Tolosa Francesc Valldeoriola Isabel Gonzalez-Aramburu Antonio Sanchez Rodriguez María Sierra Manuel Menéndez-González Marta Blazquez Ciara Garcia Esther Suarez-San Martin Pedro García-Ruiz Juan Carlos Martínez-Castrillo Lydia Vela-Desojo Clara Ruz Francisco Javier Barrero Francisco Escamilla-Sevilla Adolfo Mínguez-Castellanos Debora Cerdan Cesar Tabernero Maria Jose Gomez Heredia Francisco Perez Errazquin Manolo Romero-Acebal Cici Feliz Jose Luis Lopez-Sendon Marina Mata Irene Martínez Torres Jonggeol Jeffrey Kim Clifton L Dalgard Janet Brooks Sara Saez-Atienzar J Raphael Gibbs Rafael Jorda Juan A Botia Luis Bonet-Ponce Karen E Morrison Carl Clarke Manuela Tan Huw Morris Connor Edsall Dena Hernandez Javier Simon-Sanchez Mike A Nalls Sonja W Scholz Adriano Jimenez-Escrig Jacinto Duarte Francisco Vives Raquel Duran Janet Hoenicka Victoria Alvarez Jon Infante Maria José Marti Jordi Clarimón Adolfo López de Munain Pau Pastor Pablo Mir Andrew Singleton

Mov Disord 2019 12 29;34(12):1851-1863. Epub 2019 Oct 29.

Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/mds.27864DOI Listing
December 2019

POLR3A-related spastic ataxia: new mutations and a look into the phenotype.

J Neurol 2020 Feb 21;267(2):324-330. Epub 2019 Oct 21.

Neurogenetics Laboratory, Functional and Translational Neurogenetics Unit, Department of Neuroscience, Germans Trias i Pujol Research Institute (IGTP), Universitat Autònoma de Barcelona-Can Ruti Campus, Badalona, Barcelona, Spain.

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http://dx.doi.org/10.1007/s00415-019-09574-9DOI Listing
February 2020

Analysis of Visuospatial Abilities in Chiari Malformation Type I.

Cerebellum 2020 Feb;19(1):6-15

Neurology Service, University Hospital Marqués de Valdecilla, IDIVAL, University of Cantabria, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas-CIBERNED, Santander, Spain.

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http://dx.doi.org/10.1007/s12311-019-01056-yDOI Listing
February 2020

Persistent isolated mydriasis as an early sign of internal carotid artery dissection: Pourfour du petit syndrome.

Clin Neurol Neurosurg 2019 07 1;182:70-72. Epub 2019 May 1.

Service of Neurology, University Hospital "Marqués de Valdecilla" - IDIVAL - University of Cantabria. Santander, Spain; "Centro de Investigación de red de enfermedades neurodegenerativas (CIBERNED)". Spain.

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http://dx.doi.org/10.1016/j.clineuro.2019.04.030DOI Listing
July 2019

A unicenter, prospective study of Guillain-Barré syndrome in Spain.

Acta Neurol Scand 2019 Jun 10;139(6):546-554. Epub 2019 Apr 10.

Service of Neurology, University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, and "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", Santander, Spain.

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http://dx.doi.org/10.1111/ane.13092DOI Listing
June 2019

Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) with chronic cough and preserved muscle stretch reflexes: evidence for selective sparing of afferent Ia fibres.

J Neurol 2018 Jun 25;265(6):1454-1462. Epub 2018 Apr 25.

Service of Neurology, University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria, and "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", Santander, Spain.

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http://link.springer.com/10.1007/s00415-018-8872-1
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http://dx.doi.org/10.1007/s00415-018-8872-1DOI Listing
June 2018

α-synuclein (SNCA) but not dynamin 3 (DNM3) influences age at onset of leucine-rich repeat kinase 2 (LRRK2) Parkinson's disease in Spain.

Mov Disord 2018 04 23;33(4):637-641. Epub 2018 Feb 23.

Laboratory of Parkinson Disease and Other Neurodegenerative Movement Disorders, Clinical and Experimental Research, Department of Neurology, Hospital Clínic of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain.

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http://dx.doi.org/10.1002/mds.27295DOI Listing
April 2018

Prospective clinical and DaT-SPECT imaging in premotor G2019S-associated Parkinson disease.

Neurology 2017 Aug 5;89(5):439-444. Epub 2017 Jul 5.

From the Neurology Service (M.S., P.S.-J., I.G.-A., A.S.-R., J.B., J.I.), University Hospital Marqués de Valdecilla and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), IDIVAL, University of Cantabria (UC); and Nuclear Medicine Department (I.M.-R., M.J.-A., I.B.). Molecular Imaging Group (IDIVAL), University Hospital Marqués de Valdecilla, Santander, Spain.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000004185DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5539730PMC
August 2017

Oculomandibular Tremor and Bilateral Hypertrophic Olivary Degeneration.

Mov Disord Clin Pract 2017 Jan-Feb;4(1):152-153. Epub 2016 May 6.

Service of Neurology University Hospital Marqués de Valdecilla Santander Spain.

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http://dx.doi.org/10.1002/mdc3.12366DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353454PMC
May 2016

Comparative blood transcriptome analysis in idiopathic and LRRK2 G2019S-associated Parkinson's disease.

Neurobiol Aging 2016 Feb 31;38:214.e1-214.e5. Epub 2015 Oct 31.

Institute of Biomedicine and Biotechnology of Cantabria (IBBTEC), Spanish National Research Council (CSIC), Santander, Spain.

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http://dx.doi.org/10.1016/j.neurobiolaging.2015.10.026DOI Listing
February 2016

NEFL N98S mutation: another cause of dominant intermediate Charcot-Marie-Tooth disease with heterogeneous early-onset phenotype.

J Neurol 2016 Feb 8;263(2):361-369. Epub 2015 Dec 8.

Molecular Neurogenomics Group, VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00415-015-7985-zDOI Listing
February 2016

NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.

J Neurol 2015 May 1;262(5):1289-300. Epub 2015 Apr 1.

Service of Neurology, University Hospital "Marqués de Valdecilla (IDIVAL)", University of Cantabria (UC) and "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", Santander, Spain,

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http://dx.doi.org/10.1007/s00415-015-7709-4DOI Listing
May 2015

Identification of candidate genes for Parkinson's disease through blood transcriptome analysis in LRRK2-G2019S carriers, idiopathic cases, and controls.

Neurobiol Aging 2015 Feb 5;36(2):1105-9. Epub 2014 Nov 5.

Institute of Biomedicine and Biotechnology of Cantabria, Spanish National Research Council (CSIC), Santander, Spain.

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http://dx.doi.org/10.1016/j.neurobiolaging.2014.10.039DOI Listing
February 2015

The onset of nonmotor symptoms in Parkinson's disease (the ONSET PD study).

Mov Disord 2015 Feb 1;30(2):229-37. Epub 2014 Dec 1.

Neurology Service, Hospital Clínic de Barcelona, Universitat de Barcelona, IDIBAPS, Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Catalonia, Spain.

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http://dx.doi.org/10.1002/mds.26077DOI Listing
February 2015

Nonmotor symptoms in LRRK2 G2019S associated Parkinson's disease.

PLoS One 2014 17;9(10):e108982. Epub 2014 Oct 17.

Parkinson's Disease and Movement Disorders Unit, Neurology Service, Institut de Neurociències Hospital Clínic, University of Barcelona, Barcelona, Spain; Institut d'investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0108982PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201457PMC
July 2015

Serum uric acid and risk of dementia in Parkinson's disease.

Parkinsonism Relat Disord 2014 Jun 5;20(6):637-9. Epub 2014 Mar 5.

Service of Neurology, Universitary Hospital Marqués de Valdecilla (IFIMAV), University of Cantabria (UC), Santander, Spain; Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Spain. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2014.02.023DOI Listing
June 2014

Evolution of Charcot-Marie-Tooth disease type 1A duplication: a 2-year clinico-electrophysiological and lower-limb muscle MRI longitudinal study.

J Neurol 2014 Apr 22;261(4):675-85. Epub 2014 Jan 22.

Service of Neurology, University Hospital "Marqués de Valdecilla (IFIMAV)", University of Cantabria (UC) and "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", Santander, Spain.

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http://dx.doi.org/10.1007/s00415-014-7248-4DOI Listing
April 2014

Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.

Handb Clin Neurol 2013 ;115:907-32

Department of Neurology and Clinical Neurophysiology, University Hospital "Marqués de Valdecilla (IFIMAV)", University of Cantabria and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Santander, Spain. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-52902-2.00051-5DOI Listing
April 2014

Genetic variability related to serum uric acid concentration and risk of Parkinson's disease.

Mov Disord 2013 Oct 27;28(12):1737-40. Epub 2013 May 27.

Service of Neurology, Universitary Hospital Marqués de Valdecilla (IFIMAV), University of Cantabria (UC), Santander, Spain.

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http://dx.doi.org/10.1002/mds.25507DOI Listing
October 2013

[Progressive binocular diplopia].

Med Clin (Barc) 2013 Sep 13;141(6):e11. Epub 2013 May 13.

Servicio de Neurología, Hospital Universitario Marqués de Valdecilla (IFIMAV), Universidad de Cantabria, Santander, España; Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), Madrid, España. Electronic address:

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http://dx.doi.org/10.1016/j.medcli.2013.03.011DOI Listing
September 2013

Unilateral isolated hypoglossal nerve palsy associated with internal carotid artery dissection.

J Neurol Neurosurg Psychiatry 2013 Jun 7;84(6):706. Epub 2013 Mar 7.

Service of Neurology, University Hospital "Marqués de Valdecilla", Av Valdecilla s/n, Santander 39008, Spain.

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http://dx.doi.org/10.1136/jnnp-2013-304923DOI Listing
June 2013

Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease.

Neurology 2013 Feb 16;80(7):621-6. Epub 2013 Jan 16.

Neurology Service, Universitary Hospital Marqués de Valdecilla and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, Spain.

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http://dx.doi.org/10.1212/WNL.0b013e31828250d6DOI Listing
February 2013

Substantia nigra echogenicity in Friedreich's ataxia patients.

Cerebellum 2013 Aug;12(4):437-40

Service of Neurology, University Hospital Marqués de Valdecilla (IFIMAV), 39008, Santander, Spain.

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http://dx.doi.org/10.1007/s12311-012-0434-yDOI Listing
August 2013

[Controversial aspects in WHO grade II gliomas management: review of recent literature].

Rev Neurol 2011 Dec;53(12):747-57

Servicio de Neurología, Hospital Universitario Marqués de Valdecilla e Instituto de Formación e Investigación Marqués de Valdecilla, Santander, Cantabria, España.

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December 2011

Magnetic resonance imaging of lower limb musculature in acute motor axonal neuropathy.

J Neurol 2012 Jun 23;259(6):1111-6. Epub 2011 Nov 23.

Service of Neurology, University Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain.

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http://dx.doi.org/10.1007/s00415-011-6309-1DOI Listing
June 2012

Subclinical Charcot-Marie-Tooth disease type 1A in an ex-professional cyclist.

Clin Neurol Neurosurg 2012 May 21;114(4):394-5. Epub 2011 Nov 21.

Service of Neurology, University Hospital Marqués de Valdecilla (IFIMAV), Avda. de Valdecilla s/n, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED), University of Cantabria (UC), Santander, Spain.

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http://dx.doi.org/10.1016/j.clineuro.2011.10.041DOI Listing
May 2012

High frequency and reduced penetrance of LRRK2 G2019S mutation among Parkinson's disease patients in Cantabria (Spain).

Mov Disord 2011 Nov 27;26(13):2343-6. Epub 2011 Sep 27.

Service of Neurology, University Hospital Marqués de Valdecilla, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1002/mds.23965DOI Listing
November 2011

Mitochondrial DNA polymorphisms/haplogroups in hereditary spastic paraplegia.

J Neurol 2012 Feb 2;259(2):246-50. Epub 2011 Jul 2.

Laboratory of Molecular Genetics, Laboratory of Medicine, Hospital Universitario Central de Asturias, 33006, Oviedo, Spain.

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http://dx.doi.org/10.1007/s00415-011-6155-1DOI Listing
February 2012

New insights into the pathophysiology of pes cavus in Charcot-Marie-Tooth disease type 1A duplication.

J Neurol 2011 Sep 18;258(9):1594-602. Epub 2011 May 18.

Service of Neurology, University Hospital "Marqués de Valdecilla" (IFIMAV), "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas (CIBERNED)", University of Cantabria (UC), 39008 Santander, Spain.

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http://dx.doi.org/10.1007/s00415-011-6094-xDOI Listing
September 2011

Reduced penetrance in hereditary motor neuropathy caused by TRPV4 Arg269Cys mutation.

J Neurol 2011 Aug 19;258(8):1413-21. Epub 2011 Feb 19.

Service of Neurology, University Hospital "Marqués de Valdecilla" (IFIMAV), "Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas" (CIBERNED), University of Cantabria (UC), 39008 Santander, Spain.

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http://dx.doi.org/10.1007/s00415-011-5947-7DOI Listing
August 2011

Clinical progression in Charcot-Marie-Tooth disease type 1A duplication: clinico-electrophysiological and MRI longitudinal study of a family.

J Neurol 2010 Oct 5;257(10):1633-41. Epub 2010 May 5.

Service of Neurology, University Hospital Marqués de Valdecilla (IFIMAV), University of Cantabria and Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, 39008, Santander, Spain.

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http://link.springer.com/10.1007/s00415-010-5580-x
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http://dx.doi.org/10.1007/s00415-010-5580-xDOI Listing
October 2010

Genetic interaction between tau and the apolipoprotein E receptor LRP1 Increases Alzheimer's disease risk.

Dement Geriatr Cogn Disord 2009 13;28(2):116-20. Epub 2009 Aug 13.

Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), University Hospital Marqués de Valdecilla (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1159/000234913DOI Listing
November 2009

APOE dependent-association of PPAR-γ genetic variants with Alzheimer's disease risk.

Neurobiol Aging 2011 Mar 6;32(3):547.e1-6. Epub 2009 Aug 6.

Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Marqués de Valdecilla University Hospital-University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1016/j.neurobiolaging.2009.07.004DOI Listing
March 2011

Charcot–Marie–Tooth disease type 2J with MPZ Thr124Met mutation: clinico-electrophysiological and MRI study of a family.

J Neurol 2009 Dec;256(12):2061-71

Service of Radiology, University Hospital Marqués de Valdecilla, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, University of Cantabria, 39008 Santander, Spain.

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http://link.springer.com/10.1007/s00415-009-5251-y
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http://dx.doi.org/10.1007/s00415-009-5251-yDOI Listing
December 2009

Masseter reflex in the study of spinocerebellar ataxia type 2 and type 3.

Muscle Nerve 2009 Oct;40(4):640-2

Service of Clinical Neurophysiology, Marqués de Valdecilla, University Hospital, Centro de Investigación Biomédica en Red de Enfermedades Neurodegenerativas, 39008 Santander, Spain.

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http://doi.wiley.com/10.1002/mus.21334
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http://dx.doi.org/10.1002/mus.21334DOI Listing
October 2009

No association of CDK5 genetic variants with Alzheimer's disease risk.

BMC Med Genet 2009 Jul 17;10:68. Epub 2009 Jul 17.

Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, University Hospital Marqués de Valdecilla (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1186/1471-2350-10-68DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716333PMC
July 2009

Interaction between HMGCR and ABCA1 cholesterol-related genes modulates Alzheimer's disease risk.

Brain Res 2009 Jul 14;1280:166-71. Epub 2009 May 14.

Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1016/j.brainres.2009.05.019DOI Listing
July 2009

Synergistic effect of heme oxygenase-1 and tau genetic variants on Alzheimer's disease risk.

Dement Geriatr Cogn Disord 2008 8;26(4):339-42. Epub 2008 Oct 8.

Neurology Service, University Hospital Marqués de Valdecilla, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1159/000161059DOI Listing
February 2009

Gene-gene interaction between heme oxygenase-1 and liver X receptor-beta and Alzheimer's disease risk.

Neurobiol Aging 2010 Apr 1;31(4):710-4. Epub 2008 Jul 1.

Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Marqués de Valdecilla University Hospital (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1016/j.neurobiolaging.2008.05.025DOI Listing
April 2010

Periodic eye opening and swallowing movements associated with post-anoxic burst-suppression EEG pattern.

Epileptic Disord 2008 Mar;10(1):19-21

Department of Clinical Neurophysiology, Marqués de Valdecilla University Hospital (IFIMAV), Santander, Cantabria, Spain.

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http://dx.doi.org/10.1684/epd.2008.0169DOI Listing
March 2008

14-3-3 zeta and tau genes interactively decrease Alzheimer's disease risk.

Dement Geriatr Cogn Disord 2008 4;25(4):317-20. Epub 2008 Mar 4.

Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1159/000119123DOI Listing
June 2008

No association of genetic variants of liver X receptor-beta with Alzheimer's disease risk.

Am J Med Genet B Neuropsychiatr Genet 2008 Jul;147B(5):650-3

Neurology Service and Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas, Marqués de Valdecilla University Hospital (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1002/ajmg.b.30652DOI Listing
July 2008

Interaction between CD14 and LXRbeta genes modulates Alzheimer's disease risk.

J Neurol Sci 2008 Jan 27;264(1-2):97-9. Epub 2007 Sep 27.

Neurology Service, University Hospital Marqués de Valdecilla (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1016/j.jns.2007.08.001DOI Listing
January 2008

Age-dependent association of KIBRA genetic variation and Alzheimer's disease risk.

Neurobiol Aging 2009 Feb 17;30(2):322-4. Epub 2007 Aug 17.

Neurology Service, Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1016/j.neurobiolaging.2007.07.003DOI Listing
February 2009

Association of genetic variants of ABCA1 with Alzheimer's disease risk.

Am J Med Genet B Neuropsychiatr Genet 2007 Oct;144B(7):964-8

Neurology Service, Marqués de Valdecilla University Hospital (University of Cantabria), 39008 Santander, Spain.

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http://dx.doi.org/10.1002/ajmg.b.30552DOI Listing
October 2007

Poly (ADP-ribose) polymerase-1 (PARP-1) genetic variants are protective against Parkinson's disease.

J Neurol Sci 2007 May 23;256(1-2):68-70. Epub 2007 Mar 23.

Service of Neurology, University Hospital Marqués de Valdecilla (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1016/j.jns.2007.02.008DOI Listing
May 2007

Interaction between poly(ADP-ribose) polymerase 1 and interleukin 1A genes is associated with Alzheimer's disease risk.

Dement Geriatr Cogn Disord 2007 9;23(4):215-8. Epub 2007 Feb 9.

Neurology Service, Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1159/000099471DOI Listing
May 2007

No association between low density lipoprotein receptor genetic variants and Alzheimer's disease risk.

Am J Med Genet B Neuropsychiatr Genet 2006 Jul;141B(5):541-3

Neurology Service, "Marqués de Valdecilla" University Hospital (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1002/ajmg.b.30341DOI Listing
July 2006

Case-control study of vascular endothelial growth factor (VEGF) genetic variability in Alzheimer's disease.

Neurosci Lett 2006 Jun 29;401(1-2):171-3. Epub 2006 Mar 29.

Service of Neurology, University Hospital "Marqués de Valdecilla" (University of Cantabria), 39008 Santander, Spain.

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http://dx.doi.org/10.1016/j.neulet.2006.03.020DOI Listing
June 2006

Stiff man-like syndrome and generalized myokymia in spinocerebellar ataxia type 3.

Mov Disord 2006 Jul;21(7):1031-5

Service of Neurology, University Hospital Marqués de Valdecilla, (UC) Santander, Spain.

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http://dx.doi.org/10.1002/mds.20865DOI Listing
July 2006

Association between glycogen synthase kinase-3beta genetic polymorphism and late-onset Alzheimer's disease.

Dement Geriatr Cogn Disord 2006 ;21(4):228-32

Neurology Service, Marqués de Valdecilla University Hospital (University of Cantabria), Santander, Spain.

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http://dx.doi.org/10.1159/000091044DOI Listing
September 2006

LRRK2 G2019S is a common mutation in Spanish patients with late-onset Parkinson's disease.

Neurosci Lett 2006 Mar 18;395(3):224-6. Epub 2005 Nov 18.

Service of Neurology, University Hospital Marqués de Valdecilla, University of Cantabria, 39008 Santander, Spain.

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http://dx.doi.org/10.1016/j.neulet.2005.10.083DOI Listing
March 2006

Very late-onset Friedreich's ataxia with minimal GAA1 expansion mimicking multiple system atrophy of cerebellar type.

Mov Disord 2005 Dec;20(12):1643-5

Department of Neurology, University Hospital Marqués de Valdecilla, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1002/mds.20644DOI Listing
December 2005

Interaction between CYP19 aromatase and butyrylcholinesterase genes increases Alzheimer's disease risk.

Dement Geriatr Cogn Disord 2005 13;20(2-3):153-7. Epub 2005 Jul 13.

Neurology Service, Marqués de Valdecilla University Hospital, University of Cantabria, Santander, Spain.

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http://dx.doi.org/10.1159/000087065DOI Listing
October 2005

CD14 receptor polymorphism and Alzheimer's disease risk.

Neurosci Lett 2005 May 20-27;380(1-2):193-6

Service of Neurology, University Hospital Marqués de Valdecilla, University of Cantabria, 39008 Santander, Spain.

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http://dx.doi.org/10.1016/j.neulet.2005.01.082DOI Listing
July 2005

Interleukin-8, intercellular adhesion molecule-1 and tumour necrosis factor-alpha gene polymorphisms and the risk for multiple system atrophy.

J Neurol Sci 2005 Jan;228(1):11-3

Neurology Service, University Hospital Marqués de Valdecilla, University of Cantabria, 39008 Santander, Spain.

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http://dx.doi.org/10.1016/j.jns.2004.09.023DOI Listing
January 2005

The chemokine receptor CCR5-Delta32 gene mutation is not protective against Alzheimer's disease.

Neurosci Lett 2004 Aug;366(3):312-4

Service of Neurology, University Hospital Marqués de Valdecilla, University of Cantabria, 39008 Santander, Spain.

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http://dx.doi.org/10.1016/j.neulet.2004.05.058DOI Listing
August 2004