Publicaciones en colaboración con investigadoras/es de Hospital Universitario Araba (25)

2018

  1. Sporadic Creutzfeldt–Jakob disease with glial PrPRes nuclear and perinuclear immunoreactivity

    Neuropathology, Vol. 38, Núm. 5, pp. 561-567

2017

  1. Fatal familial insomnia: mitochondrial and protein synthesis machinery decline in the mediodorsal thalamus

    Brain Pathology, Vol. 27, Núm. 1, pp. 95-106

2016

  1. Sporadic adult-onset leucodystrophy with axonal spheroids and pigmented glia with no mutations in the known targeted genes

    Histopathology, Vol. 68, Núm. 2, pp. 308-312

  2. Síntomas no motores y motores en la enfermedad de Parkinson y su relación con la calidad de vida y los distintos subgrupos clínicos

    Neurologia, Vol. 31, Núm. 9, pp. 585-591

2015

  1. Autonomic involvement in Parkinsonian carriers of PARK2 gene mutations

    Parkinsonism and Related Disorders, Vol. 21, Núm. 7, pp. 717-722

  2. Coexistence of mixed phenotype Creutzfeldt-Jakob disease, Lewy body disease and argyrophilic grain disease plus histological features of possible Alzheimer's disease: A multi-protein disorder in an autopsy case

    Neuropathology, Vol. 35, Núm. 1, pp. 56-63

  3. Cognitive and behavioral symptoms in Parkinson's disease patients with the G2019S and R1441G mutations of the LRRK2 gene

    Parkinsonism and Related Disorders, Vol. 21, Núm. 5, pp. 494-499

2014

  1. Impulse control and repetitive behaviors in Parkinson's disease - Are there differences in the relation to dopamine agonist treatment?

    Journal of the Neurological Sciences

2013

  1. A novel form of human disease

    Prion Biology: Research and Advances (Apple Academic Press), pp. 179-210

  2. Autonomic dysfunction in parkinsonian LRRK2 mutation carriers

    Parkinsonism and Related Disorders, Vol. 19, Núm. 10, pp. 906-909

  3. Cardiac sympathetic denervation in symptomatic and asymptomatic carriers of the E46K mutation in the α synuclein gene

    Parkinsonism and Related Disorders, Vol. 19, Núm. 1, pp. 95-100

  4. Neuropsychiatric symptoms in amnestic mild cognitive impairment: Increased risk and faster progression to dementia

    Current Alzheimer Research, Vol. 10, Núm. 1, pp. 86-94

  5. Nocturnal hypertension and dysautonomia in patients with Parkinson's disease: Are they related?

    Journal of Neurology, Vol. 260, Núm. 7, pp. 1752-1756

  6. The applause sign and neuropsychological profile in progressive supranuclear palsy and Parkinson's disease

    Clinical Neurology and Neurosurgery, Vol. 115, Núm. 8, pp. 1230-1233

2012

  1. Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: A case report

    Journal of Medical Case Reports, Vol. 6

2006

  1. Polymorphism in the cholesterol 24S-hydroxylase gene (CYP46A1) associated with the APOEε3 allele increases the risk of Alzheimer's disease and of mild cognitive impairment progressing to Alzheimer's disease

    Dementia and Geriatric Cognitive Disorders, Vol. 21, Núm. 2, pp. 81-87

  2. Tau-predominant-associated pathology in a sporadic-late-onset Hallervorden-Spatz syndrome

    Movement Disorders, Vol. 21, Núm. 1, pp. 107-111

2005

  1. A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease

    Neurology, Vol. 64, Núm. 9, pp. 1578-1585

  2. Ancestral origins of the prion protein gene D178N mutation in the Basque Country

    Human Genetics, Vol. 117, Núm. 1, pp. 61-69

  3. Familial prion diseases in the basque country (Spain)

    Neuroepidemiology, Vol. 24, Núm. 1-2, pp. 103-109