Medicina
Departamento
Renée
Ribacoba Montero
Publicaciones en las que colabora con Renée Ribacoba Montero (37)
2019
-
HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease
Neurobiology of Aging, Vol. 76, pp. 215.e9-215.e14
2017
-
Correlación de funciones ejecutivas con la lateralidad de la afectación del circuito nigro-estriatal en la enfermedad de parkinson
Libro de capítulos III Congreso Nacional de Psicología (Consejo General de la Psicología de España), pp. 45-49
-
Epilepsia mioclónica en el síndrome de Down y en la enfermedad de Alzheimer
Neurologia, Vol. 32, Núm. 2, pp. 69-73
2016
2014
-
Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms
Neuroscience Letters, Vol. 562, pp. 45-49
-
MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects
Journal of Molecular Neuroscience, Vol. 54, Núm. 4, pp. 830-836
-
The screening of the 3′UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease
Journal of Human Genetics, Vol. 59, Núm. 6, pp. 346-348
2013
-
Mutational screening of PARKIN identified a 3′ UTR variant (rs62637702) associated with parkinson's disease
Journal of Molecular Neuroscience, Vol. 50, Núm. 2, pp. 264-269
-
Profile of microRNAs in the plasma of Parkinson's disease patients and healthy controls
Journal of Neurology
2012
-
A search for SNCA 3′ UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease
Journal of Molecular Neuroscience, Vol. 47, Núm. 3, pp. 425-430
2011
-
Replication of MAPT and SNCA, but not PARK16-18, as susceptibility genes for Parkinson's disease
Movement Disorders, Vol. 26, Núm. 5, pp. 819-823
-
Vasomotor Reactivity Is Similarly Impaired in Patients with Alzheimer's Disease and Patients with Amyloid Hemorrhage
Journal of Neuroimaging, Vol. 21, Núm. 2
2010
-
Analysis of the micro-RNA-133 and PITX3 genes in Parkinson's disease
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 153, Núm. 6, pp. 1234-1239
-
Cognitive impairment in Parkinson's disease without dementia
Movement Disorders, Vol. 25, Núm. 13, pp. 2136-2141
-
FGF20 rs12720208 SNP and microRNA-433 variation: No association with Parkinson's disease in Spanish patients
Neuroscience Letters, Vol. 479, Núm. 1, pp. 22-25
-
Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia
BMC Neurology, Vol. 10
-
Partial motor status epilepticus as a clinical manifestation of carotid stenosis
International Archives of Medicine, Vol. 3, Núm. 1
2009
-
Action naming is impaired in Parkinson disease patients
Neuropsychologia, Vol. 47, Núm. 14, pp. 3271-3274
-
Mutational screening of the Mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease
Parkinsonism and Related Disorders, Vol. 15, Núm. 6, pp. 468-470
-
Mutational screening of the mortalin gene (HSPA9) in Parkinson's disease
Journal of Neural Transmission, Vol. 116, Núm. 10, pp. 1289-1293