Maria Isabel Ofelia Behrens
Maria Isabel Ofelia Behrens
Profesor Titular Neurologia Hospital Clinico Universidad de Chile
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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
A Ramirez, A Heimbach, J Gründemann, B Stiller, D Hampshire, LP Cid, ...
Nature genetics 38 (10), 1184-1191, 2006
Cancer linked to Alzheimer disease but not vascular dementia
CM Roe, AL Fitzpatrick, C Xiong, W Sieh, L Kuller, JP Miller, MM Williams, ...
Neurology 74 (2), 106-112, 2010
Alzheimer disease and cancer
CM Roe, MI Behrens, C Xiong, JP Miller, JC Morris
Neurology 64 (5), 895-898, 2005
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin‐positive, tau‐negative inclusions caused by a missense mutation in the signal peptide of progranulin
O Mukherjee, P Pastor, NJ Cairns, S Chakraverty, JSK Kauwe, S Shears, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.
C RF, H M, F RA, F S, K E, T C, C R, L C, P G, H C, K K, M A, W M, B F, ...
Nature Genetics 11 (2), 219-222, 1995
A common biological mechanism in cancer and Alzheimer's disease?
MI Behrens, C Lendon, CM Roe
Current Alzheimer Research 6 (3), 196-204, 2009
3-Nitropropionic acid induces apoptosis in cultured striatal and cortical neurons
MI Behrens, J Koh, LMT Canzoniero, SL Sensi, CA Csernansky, DW Choi
Neuroreport 6 (3), 545-548, 1995
Clinical spectrum of Kufor‐Rakeb syndrome in the Chilean kindred with ATP13A2 mutations
MI Behrens, N Brüggemann, P Chana, P Venegas, M Kägi, T Parrao, ...
Movement Disorders 25 (12), 1929-1937, 2010
Susceptibility to apoptosis is enhanced in immature cortical neurons
JW McDonald, MI Behrens, C Chung, T Bhattacharyya, DW Choi
Brain research 759 (2), 228-232, 1997
E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.
L CL, M A, B IM, K KS, M L, N J, N R, M A, B F, W M, A M, A Viana JC, O J, ...
Human Mutation 10 (3), 186-195, 1997
The serpin-enzyme complex receptor recognizes soluble, nontoxic amyloid-β peptide but not aggregated, cytotoxic amyloid-β peptide
K Boland, M Behrens, D Choi, K Manias, DH Perlmutter
Journal of Biological Chemistry 271 (30), 18032-18044, 1996
Ischemia enhances activation by Ca2+ and redox modification of ryanodine receptor channels from rat brain cortex
R Bull, JP Finkelstein, J Gálvez, G Sánchez, P Donoso, MI Behrens, ...
Journal of Neuroscience 28 (38), 9463-9472, 2008
Validation of the Spanish-language version of the Montreal Cognitive Assessment test in adults older than 60 years
C Delgado, A Araneda, MI Behrens
Neurología (English Edition) 34 (6), 376-385, 2019
Possible role of apamin‐sensitive K+ channels in myotonic dystrophy
MI Behrens, P Jalil, A Serani, F Vergara, O Alvarez
Muscle & Nerve: Official Journal of the American Association of …, 1994
Redox regulation of RyR-mediated Ca2+ release in muscle and neurons
C Hidalgo, R Bull, MI Behrens, P Donoso
Biological research 37 (4), 539-552, 2004
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype
N Brüggemann, J Hagenah, K Reetz, A Schmidt, M Kasten, I Buchmann, ...
Archives of neurology 67 (11), 1357-1363, 2010
Nonmotor symptoms in genetic Parkinson disease
M Kasten, L Kertelge, N Brüggemann, J Van Der Vegt, A Schmidt, V Tadic, ...
Archives of neurology 67 (6), 670-676, 2010
ATP13A2 variants in early‐onset Parkinson's disease patients and controls
A Djarmati, J Hagenah, K Reetz, S Winkler, MI Behrens, H Pawlack, ...
Movement disorders: official journal of the Movement Disorder Society 24 (14 …, 2009
Validación del instrumento Montreal Cognitive Assessment en español en adultos mayores de 60 años
C Delgado, A Araneda, MI Behrens
Neurología 34 (6), 376-385, 2019
Mitochondrial permeability transition pore contributes to mitochondrial dysfunction in fibroblasts of patients with sporadic Alzheimer's disease
MJ Pérez, DP Ponce, A Aranguiz, MI Behrens, RA Quintanilla
Redox Biology 19, 290-300, 2018
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