Alberto Lleó Bisa

Alberto Lleó

Dr. Alberto Lleó is the director of the Memory Unit of the Neurology Department at Hospital de la Santa Creu i Sant Pau.

After obtaining his Medical degree from the University of Barcelona, he completed his specialization in Neurology at Hospital de la Santa Creu i Sant Pau in 2000. Two years later, he obtained his PhD in Medicine at the University of Barcelona and continued his education with a clinical and basic research fellowship on memory and movement disorders at the Massachusetts General Hospital, Boston (2002-2004) where he combined clinical and research tasks.

In his professional career, Dr. Alberto Lleó has combined his clinical activity with translational research projects in the field of dementias with a specific focus on the molecular bases of the disease and biomarker development. Some of his main contributions are the discovery of new genetic alterations in Alzheimer’s disease, the study of the gamma-secretase complex, and the assessment of new chemical biomarkers for Alzheimer’s disease and frontotemporal dementia.

Today, Dr. Alberto Lleó runs a translational group, leads many projects funded by public and private agencies, and collaborates regularly with numerous national and international research groups. He also coordinates the Alzheimer program of CIBERNED (Center for Networked Biomedical Research in Neurodegenerative Diseases). To date, he has authored more than 20 book chapters and over 150 publications in international journals, and his contributions have been awarded by the Spanish Society of Neurology.

Recent Publications

  1. Sex differences in the behavioral variant of frontotemporal dementia: A new window to executive and behavioral reserve. Illán-Gala, I, Casaletto, KB, Borrego-Écija, S et al. Alzheimers Dement 2021
    PMID:33590953

  2. Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Chia, R, Sabir, MS, Bandres-Ciga, S et al. Nat Genet 2021
    PMID:33589841

  3. Pathophysiological subtypes of Alzheimer's disease based on cerebrospinal fluid proteomics. Tijms, BM, Gobom, J, Reus, L et al. Brain 2020
    PMID:33439986

  4. White Matter Hyperintensities Are No Major Confounder for Alzheimer's Disease Cerebrospinal Fluid Biomarkers. van Waalwijk van Doorn, LJC, Ghafoorian, M, van Leijsen, EMC et al. J Alzheimers Dis 2021
    PMID:33252070

  5. Nerve growth factor (NGF) pathway biomarkers in Down syndrome prior to and after the onset of clinical Alzheimer's disease: A paired CSF and plasma study. Pentz, R, Iulita, MF, Ducatenzeiler, A et al. Alzheimers Dement 2020
    PMID:33226181

  6. Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Hong, S, Prokopenko, D, Dobricic, V et al. Transl Psychiatry 2020
    PMID:33223526

  7. Plasma Tau and Neurofilament Light in Frontotemporal Lobar Degeneration and Alzheimer Disease. Illán-Gala, I, Lleo, A, Karydas, A et al. Neurology 2021
    PMID:33199433

  8. Biphasic cortical macro- and microstructural changes in autosomal dominant Alzheimer's disease. Montal, V, Vilaplana, E, Pegueroles, J et al. Alzheimers Dement 2020
    PMID:33196147

  9. Cerebrospinal fluid total tau levels indicate aberrant neuronal plasticity in Alzheimer's disease. Visser, PJ, Reus, LM, Gobom, J et al. medRxiv 2020
    PMID:33173883

  10. Serum neurofilament light chain predicts long-term prognosis in Guillain-Barré syndrome patients. Martín-Aguilar, L, Camps-Renom, P, Lleixà, C et al. J Neurol Neurosurg Psychiatry 2020
    PMID:33154183

  11. Dementia and epilepsy: Not a one-way street. Hauser, WA, Lleo, A, Schmolck, H et al. Neurology 2020
    PMID:33097601

  12. Heterozygous APOE Christchurch in familial Alzheimer's disease without mutations in other Mendelian genes. Hernandez, I, Gelpi, E, Molina-Porcel, L et al. Neuropathol Appl Neurobiol 2020
    PMID:33095930

  13. Cerebrospinal fluid A beta 1-40 peptides increase in Alzheimer's disease and are highly correlated with phospho-tau in control individuals. Lehmann, S, Dumurgier, J, Ayrignac, X et al. Alzheimers Res Ther 2020
    PMID:33008460

  14. Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia. Rosas, I, Martínez, C, Coto, E et al. Neurobiol Aging 2021
    PMID:32972771

  15. C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts. Costa, B, Manzoni, C, Bernal-Quiros, M et al. Neurology 2020
    PMID:32943482

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