Detalles de la búsqueda
1.
NFKB1 variants were associated with the risk of Parkinson´s disease in male.
J Neural Transm (Vienna)
; 2024 Feb 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-38416198
2.
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Mov Disord
; 38(2): 286-303, 2023 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-36692014
3.
Toward a new nosology of neurodegenerative diseases.
Alzheimers Dement
; 19(8): 3731-3737, 2023 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-36960767
4.
Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.
Int J Mol Sci
; 24(2)2023 Jan 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36674414
5.
Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies.
Mov Disord
; 37(9): 1841-1849, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35852957
6.
New, Fully Implantable Device for Selective Clearance of CSF-Target Molecules: Proof of Concept in a Murine Model of Alzheimer's Disease.
Int J Mol Sci
; 23(16)2022 Aug 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-36012525
7.
Cancer in Parkinson's Disease: An Approximation to the Main Risk Factors.
Neurodegener Dis
; 21(1-2): 36-41, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34673649
8.
Prevalence of Depression and Anxiety in Parkinson Disease and Impact on Quality of Life: A Community-Based Study in Spain.
J Geriatr Psychiatry Neurol
; 33(4): 207-213, 2020 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-31597514
9.
Perrault syndrome with neurological features in a compound heterozygote for two TWNK mutations: overlap of TWNK-related recessive disorders.
J Transl Med
; 17(1): 290, 2019 08 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-31455392
10.
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight.
Mov Disord
; 34(12): 1851-1863, 2019 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-31660654
11.
Neuropsychological Test Performance in Parkinsonism Without Dopaminergic Deficiency on [123I]-FP-CIT SPECT Imaging.
J Int Neuropsychol Soc
; 24(6): 646-651, 2018 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29669609
12.
Lipid-specific immunoglobulin M bands in cerebrospinal fluid are associated with a reduced risk of developing progressive multifocal leukoencephalopathy during treatment with natalizumab.
Ann Neurol
; 77(3): 447-57, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25581547
13.
Huntingtin CAG repeats in neuropathologically confirmed tauopathies: Novel insights.
Brain Pathol
; : e13250, 2024 Feb 28.
Artículo
en Inglés
| MEDLINE | ID: mdl-38418081
14.
Levodopa-Induced Dyskinesias are Frequent and Impact Quality of Life in Parkinson's Disease: A 5-Year Follow-Up Study.
Mov Disord Clin Pract
; 2024 May 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-38747234
15.
Mechanical filtration of the cerebrospinal fluid: procedures, systems, and applications.
Expert Rev Med Devices
; 20(3): 199-207, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36799735
16.
A Nanostructured Protein Filtration Device for Possible Use in the Treatment of Alzheimer's Disease-Concept and Feasibility after In Vivo Tests.
Bioengineering (Basel)
; 10(11)2023 Nov 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-38002427
17.
Refining Stereotaxic Neurosurgery Techniques and Welfare Assessment for Long-Term Intracerebroventricular Device Implantation in Rodents.
Animals (Basel)
; 13(16)2023 Aug 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-37627418
18.
Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Neurol Genet
; 9(4): e200079, 2023 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-37293291
19.
Erratum: Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Neurol Genet
; 9(5): e200095, 2023 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-37521204
20.
Sex Differences in Motor and Non-Motor Symptoms among Spanish Patients with Parkinson's Disease.
J Clin Med
; 12(4)2023 Feb 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36835866