Luengo A - Search Results

1

Genetic variability of histamine receptors in patients with Parkinson's disease.

García-Martín E, Ayuso P, Luengo A, Martínez C, Agúndez JA. García-Martín E, et al. Among authors: luengo a. BMC Med Genet. 2008 Mar 17;9:15. doi: 10.1186/1471-2350-9-15. BMC Med Genet. 2008. PMID: 18366640 Free PMC article.

2

Nonsynonymous polymorphisms of histamine-metabolising enzymes in patients with Parkinson's disease.

Agúndez JA, Luengo A, Herráez O, Martínez C, Alonso-Navarro H, Jiménez-Jiménez FJ, García-Martín E. Agúndez JA, et al. Among authors: luengo a. Neuromolecular Med. 2008;10(1):10-6. doi: 10.1007/s12017-007-8017-7. Epub 2007 Nov 6. Neuromolecular Med. 2008. PMID: 17985251

3

A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.

Ayuso P, Martínez C, Lorenzo-Betancor O, Pastor P, Luengo A, Jiménez-Jiménez FJ, Alonso-Navarro H, Villalba MT, Agúndez JA, García-Martín E. Ayuso P, et al. Among authors: luengo a. Pharmacogenet Genomics. 2011 Sep;21(9):565-71. doi: 10.1097/FPC.0b013e328348f729. Pharmacogenet Genomics. 2011. PMID: 21709601

4

LINGO1 gene analysis in Parkinson's disease phenotypes.

Lorenzo-Betancor O, Samaranch L, García-Martín E, Cervantes S, Agúndez JA, Jiménez-Jiménez FJ, Alonso-Navarro H, Luengo A, Coria F, Lorenzo E, Irigoyen J, Pastor P; Iberian Parkinson's Disease Genetics Study Group Researchers. Lorenzo-Betancor O, et al. Among authors: luengo a. Mov Disord. 2011 Mar;26(4):722-7. doi: 10.1002/mds.23452. Epub 2011 Jan 4. Mov Disord. 2011. PMID: 21506150

5

An association study between Heme oxygenase-1 genetic variants and Parkinson's disease.

Ayuso P, Martínez C, Pastor P, Lorenzo-Betancor O, Luengo A, Jiménez-Jiménez FJ, Alonso-Navarro H, Agúndez JA, García-Martín E. Ayuso P, et al. Among authors: luengo a. Front Cell Neurosci. 2014 Sep 24;8:298. doi: 10.3389/fncel.2014.00298. eCollection 2014. Front Cell Neurosci. 2014. PMID: 25309329 Free PMC article.

6

Association between the oxidative polymorphism and early onset of Parkinson's disease.

Agúndez JA, Jiménez-Jiménez FJ, Luengo A, Bernal ML, Molina JA, Ayuso L, Vázquez A, Parra J, Duarte J, Coria F, et al. Agúndez JA, et al. Among authors: luengo a. Clin Pharmacol Ther. 1995 Mar;57(3):291-8. doi: 10.1016/0009-9236(95)90154-X. Clin Pharmacol Ther. 1995. PMID: 7697946

7

Slow allotypic variants of the NAT2 gene and susceptibility to early-onset Parkinson's disease.

Agúndez JA, Jiménez-Jiménez FJ, Luengo A, Molina JA, Ortí-Pareja M, Vázquez A, Ramos F, Duarte J, Coria F, Ladero JM, Alvarez-Cermeño JC, Benítez J. Agúndez JA, et al. Among authors: luengo a. Neurology. 1998 Dec;51(6):1587-92. doi: 10.1212/wnl.51.6.1587. Neurology. 1998. PMID: 9855506

8

Lack of association of LINGO1 rs9652490 and rs11856808 SNPs with familial essential tremor.

Lorenzo-Betancor O, García-Martín E, Cervantes S, Agúndez JA, Jiménez-Jiménez FJ, Alonso-Navarro H, Luengo A, Coria F, Lorenzo E, Irigoyen J, Pastor P. Lorenzo-Betancor O, et al. Among authors: luengo a. Eur J Neurol. 2011 Aug;18(8):1085-9. doi: 10.1111/j.1468-1331.2010.03251.x. Epub 2010 Nov 18. Eur J Neurol. 2011. PMID: 21219542

9

LINGO1 rs9652490 and rs11856808 are not associated with the risk of Parkinson's disease: results of a meta-analysis.

Agúndez JA, Lorenzo-Betancor O, Pastor P, García-Martín E, Luengo A, Alonso-Navarro H, Jiménez-Jiménez FJ. Agúndez JA, et al. Among authors: luengo a. Parkinsonism Relat Disord. 2012 Jun;18(5):657-9. doi: 10.1016/j.parkreldis.2011.09.005. Epub 2011 Sep 28. Parkinsonism Relat Disord. 2012. PMID: 21955595 No abstract available.

10

Caffeine demethylase activity in human and Dark Agouti rat liver microsomes. Comparison with aminopyrine N-demethylase activity.

Agúndez JA, Luengo A, Benítez J. Agúndez JA, et al. Among authors: luengo a. Drug Metab Dispos. 1992 May-Jun;20(3):343-9. Drug Metab Dispos. 1992. PMID: 1521502

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