B. Atarés

发表

The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia

J. Hoenicka, T. del Ser, D. Munoz, 2004, Annals of neurology.

P. Pástor, B. Puig, I. Ferrer, 2005, Neurology.

A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

I. Ferrer, M. D. de Pancorbo, J. Zarranz, 2010, BMC neurology.

Phenotypic variability in familial prion diseases due to the D178N mutation

M. Pancorbo, M. D. de Pancorbo, A. López de Munain, 2005, Journal of Neurology, Neurosurgery & Psychiatry.

Familial Prion Diseases in the Basque Country (Spain)

J. Zarranz, M. Fernández-Martínez, J. Martí-Massó, 2004, Neuroepidemiology.

A Novel PRNP Y218N Mutation in Gerstmann-Sträussler-Scheinker Disease With Neurofibrillary Degeneration

I. Ferrer, A. López de Munain, A. Gorostidi, 2010, Journal of neuropathology and experimental neurology.

Molecularly determined total tumour load in lymph nodes of stage I–II colon cancer patients correlates with high-risk factors. A multicentre prospective study

X. Matías-Guiu, M. Méndez, J. Zamora, 2016, Virchows Archiv.

Dementia, amyotrophy, and periodic complexes on the electroencephalogram: a diagnostic challenge.

J. Zarranz, B. Atarés, F. Velasco, 2001, Archives of neurology.

Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt–Jakob disease: a case report

I. Ferrer, A. L. de Munain, J. Zarranz, 2012, Journal of Medical Case Reports.

Value of limited necropsy in HIV-positive patients.

I. Guerra, M. Aldamiz-Etxebarría, B. Atarés, 2001, Pathology, research and practice.

M. D’Amato, I. Gutiérrez-Ibarluzea, J. Banales, 2018, European journal of public health.

Population-based colorectal cancer screening programmes using a faecal immunochemical test: should faecal haemoglobin cut-offs differ by age and sex?

I. Gutiérrez-Ibarluzea, Á. Calderón, L. Bujanda, 2017, BMC Cancer.

Tau‐predominant–associated pathology in a sporadic late‐onset Hallervorden–Spatz syndrome

J. Zarranz, J. Gómez-Esteban, E. Lezcano, 2006, Movement disorders : official journal of the Movement Disorder Society.

Somatic mosaicism in a case of apparently sporadic Creutzfeldt‐Jakob disease carrying a de novo D178N mutation in the PRNP gene

I. Ferrer, M. Pancorbo, I. Ferrer, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Parkinson's disease‐like presentation of multiple system atrophy with poor response to STN stimulation: A clinicopathological case report

J. Zarranz, J. Gómez-Esteban, Elena Lezcano, 2004, Movement disorders : official journal of the Movement Disorder Society.