Lleó A - Search Results

1

Metabolite Signature of Alzheimer's Disease in Adults with Down Syndrome.

Montal V, Barroeta I, Bejanin A, Pegueroles J, Carmona-Iragui M, Altuna M, Benejam B, Videla L, Fernández S, Padilla C, Aranha MR, Iulita MF, Vidal-Piñeiro D, Alcolea D, Blesa R, Lleó A, Fortea J; Down Alzheimer Barcelona Neuroimaging Initiative. Montal V, et al. Among authors: lleo a. Ann Neurol. 2021 Sep;90(3):407-416. doi: 10.1002/ana.26178. Epub 2021 Aug 6. Ann Neurol. 2021. PMID: 34309066

2

Uncommon polymorphism in the presenilin genes in human familial Alzheimer's disease: not to be mistaken with a pathogenic mutation.

Lleó A, Castellví M, Blesa R, Oliva R. Lleó A, et al. Neurosci Lett. 2002 Feb 1;318(3):166-8. doi: 10.1016/s0304-3940(01)02499-5. Neurosci Lett. 2002. PMID: 11803125

3

[Clinical characteristics of a family with early-onset Alzheimer's disease associated with a presenilin 1 mutation (M139T)].

Lleó A, Blesa R, Gendre J, Castellví M, Molinuevo JL, Oliva R. Lleó A, et al. Med Clin (Barc). 2002 May 18;118(18):698-700. doi: 10.1016/s0025-7753(02)72501-3. Med Clin (Barc). 2002. PMID: 12042135 Spanish.

4

Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain.

Lleó A, Blesa R, Queralt R, Ezquerra M, Molinuevo JL, Peña-Casanova J, Rojo A, Oliva R. Lleó A, et al. Arch Neurol. 2002 Nov;59(11):1759-63. doi: 10.1001/archneur.59.11.1759. Arch Neurol. 2002. PMID: 12433263

5

A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.

Ezquerra M, Lleó A, Castellví M, Queralt R, Santacruz P, Pastor P, Molinuevo JL, Blesa R, Oliva R. Ezquerra M, et al. Among authors: lleo a. Arch Neurol. 2003 Aug;60(8):1149-51. doi: 10.1001/archneur.60.8.1149. Arch Neurol. 2003. PMID: 12925374

6

Emotional reactions to predictive testing in Alzheimer's disease and other inherited dementias.

Molinuevo JL, Pintor L, Peri JM, Lleó A, Oliva R, Marcos T, Blesa R. Molinuevo JL, et al. Among authors: lleo a. Am J Alzheimers Dis Other Demen. 2005 Jul-Aug;20(4):233-8. doi: 10.1177/153331750502000408. Am J Alzheimers Dis Other Demen. 2005. PMID: 16136847 Free PMC article.

7

Homocysteine and cognitive impairment. Relation with diagnosis and neuropsychological performance.

Sala I, Belén Sánchez-Saudinós M, Molina-Porcel L, Lázaro E, Gich I, Clarimón J, Blanco-Vaca F, Blesa R, Gómez-Isla T, Lleó A. Sala I, et al. Among authors: lleo a. Dement Geriatr Cogn Disord. 2008;26(6):506-12. doi: 10.1159/000173710. Epub 2008 Nov 20. Dement Geriatr Cogn Disord. 2008. PMID: 19023204

8

Early-onset familial lewy body dementia with extensive tauopathy: a clinical, genetic, and neuropathological study.

Clarimón J, Molina-Porcel L, Gómez-Isla T, Blesa R, Guardia-Laguarta C, González-Neira A, Estorch M, Ma Grau J, Barraquer L, Roig C, Ferrer I, Lleó A. Clarimón J, et al. Among authors: lleo a. J Neuropathol Exp Neurol. 2009 Jan;68(1):73-82. doi: 10.1097/NEN.0b013e3181927577. J Neuropathol Exp Neurol. 2009. PMID: 19104444

9

Mild cholesterol depletion reduces amyloid-beta production by impairing APP trafficking to the cell surface.

Guardia-Laguarta C, Coma M, Pera M, Clarimón J, Sereno L, Agulló JM, Molina-Porcel L, Gallardo E, Deng A, Berezovska O, Hyman BT, Blesa R, Gómez-Isla T, Lleó A. Guardia-Laguarta C, et al. Among authors: lleo a. J Neurochem. 2009 Jul;110(1):220-30. doi: 10.1111/j.1471-4159.2009.06126.x. Epub 2009 Apr 27. J Neurochem. 2009. PMID: 19457132 Free PMC article.

10

Clinical, neuropathologic, and biochemical profile of the amyloid precursor protein I716F mutation.

Guardia-Laguarta C, Pera M, Clarimón J, Molinuevo JL, Sánchez-Valle R, Lladó A, Coma M, Gómez-Isla T, Blesa R, Ferrer I, Lleó A. Guardia-Laguarta C, et al. Among authors: lleo a. J Neuropathol Exp Neurol. 2010 Jan;69(1):53-9. doi: 10.1097/NEN.0b013e3181c6b84d. J Neuropathol Exp Neurol. 2010. PMID: 20010303

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