Lleó A - Search Results

1

Pathophysiological Underpinnings of Extra-Motor Neurodegeneration in Amyotrophic Lateral Sclerosis: New Insights From Biomarker Studies.

Reyes-Leiva D, Dols-Icardo O, Sirisi S, Cortés-Vicente E, Turon-Sans J, de Luna N, Blesa R, Belbin O, Montal V, Alcolea D, Fortea J, Lleó A, Rojas-García R, Illán-Gala I. Reyes-Leiva D, et al. Among authors: lleo a. Front Neurol. 2022 Jan 18;12:750543. doi: 10.3389/fneur.2021.750543. eCollection 2021. Front Neurol. 2022. PMID: 35115992 Free PMC article. Review.

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

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

7

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

8

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.

9

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

10

Dementia risk in Parkinson disease: disentangling the role of MAPT haplotypes.

Setó-Salvia N, Clarimón J, Pagonabarraga J, Pascual-Sedano B, Campolongo A, Combarros O, Mateo JI, Regaña D, Martínez-Corral M, Marquié M, Alcolea D, Suárez-Calvet M, Molina-Porcel L, Dols O, Gómez-Isla T, Blesa R, Lleó A, Kulisevsky J. Setó-Salvia N, et al. Among authors: lleo a. Arch Neurol. 2011 Mar;68(3):359-64. doi: 10.1001/archneurol.2011.17. Arch Neurol. 2011. PMID: 21403021

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