María Cruz
Rodríguez Oroz
Consultora Médica
Universidad del País Vasco/Euskal Herriko Unibertsitatea
Lejona, EspañaPublicacións en colaboración con investigadores/as de Universidad del País Vasco/Euskal Herriko Unibertsitatea (12)
2023
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Hippocampal synaptic failure is an early event in experimental parkinsonism with subtle cognitive deficit
Brain : a journal of neurology, Vol. 146, Núm. 12, pp. 4949-4963
2022
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Striatal synaptic bioenergetic and autophagic decline in premotor experimental parkinsonism
Brain, Vol. 145, Núm. 6, pp. 2092-2107
2020
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Correction to: Motor impulsivity and delay intolerance are elicited in a dose-dependent manner with a dopaminergic agonist in parkinsonian rats (Psychopharmacology, (2020), 237, 8, (2419-2431), 10.1007/s00213-020-05544-6)
Psychopharmacology
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Motor impulsivity and delay intolerance are elicited in a dose-dependent manner with a dopaminergic agonist in parkinsonian rats
Psychopharmacology, Vol. 237, Núm. 8, pp. 2419-2431
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[18F]-DPA-714 PET as a specific in vivo marker of early microglial activation in a rat model of progressive dopaminergic degeneration
European Journal of Nuclear Medicine and Molecular Imaging, Vol. 47, Núm. 11, pp. 2602-2612
2019
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Pramipexole-induced impulsivity in mildparkinsonian rats: a model of impulse control disorders in Parkinson's disease
Neurobiology of Aging, Vol. 75, pp. 126-135
2018
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Using Kinect to classify Parkinson's disease stages related to severity of gait impairment
BMC Bioinformatics, Vol. 19, Núm. 1
2016
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DAT imaging and clinical biomarkers in relatives at genetic risk for LRRK2R1441G Parkinson's disease
Movement Disorders, Vol. 31, Núm. 3, pp. 335-343
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Genetic Mutation Analysis of Parkinson’s Disease Patients Using Multigene Next-Generation Sequencing Panels
Molecular Diagnosis and Therapy, Vol. 20, Núm. 5, pp. 481-491
2015
2014
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Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2
Parkinsonism and Related Disorders, Vol. 20, Núm. 10, pp. 1097-1100
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Prevalence of cancer in Parkinson's disease related to R1441G and G2019S mutations in LRRK2
Movement Disorders, Vol. 29, Núm. 6, pp. 750-755