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357 results

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Page 1
Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy.
Ayerdi-Izquierdo A, Stavrides G, Sellés-Martínez JJ, Larrea L, Bovo G, López de Munain A, Bisulli F, Martí-Massó JF, Michelucci R, Poza JJ, Tinuper P, Stephani U, Striano P, Striano S, Staub E, Sarafidou T, Hinzmann B, Moschonas N, Siebert R, Deloukas P, Nobile C, Pérez-Tur J. Ayerdi-Izquierdo A, et al. Among authors: lopez de munain a. Epilepsy Res. 2006 Aug;70(2-3):118-26. doi: 10.1016/j.eplepsyres.2006.03.008. Epub 2006 May 16. Epilepsy Res. 2006. PMID: 16707245 Free article.
Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia.
Nobile C, Hinzmann B, Scannapieco P, Siebert R, Zimbello R, Perez-Tur J, Sarafidou T, Moschonas NK, French L, Deloukas P, Ciccodicola A, Gesk S, Poza JJ, Lo Nigro C, Seri M, Schlegelberger B, Rosenthal A, Valle G, Lopez de Munain A, Tassinari CA, Michelucci R. Nobile C, et al. Among authors: lopez de munain a. Gene. 2002 Jan 9;282(1-2):87-94. doi: 10.1016/s0378-1119(01)00846-0. Gene. 2002. PMID: 11814680
[Basic concepts in molecular genetics].
Cobo AM, Poza JJ, Sáenz A, López de Munain A. Cobo AM, et al. Among authors: lopez de munain a. Rev Neurol. 1996 Mar;24(127):315-9. Rev Neurol. 1996. PMID: 8742399 Review. Spanish. No abstract available.
Apolipoprotein E epsilon4 allele in familial and sporadic Parkinson's disease.
Blázquez L, Otaegui D, Sáenz A, Paisán-Ruiz C, Emparanza JI, Ruiz-Martinez J, Moreno F, Martí-Massó JF, López de Munain A. Blázquez L, et al. Among authors: lopez de munain a. Neurosci Lett. 2006 Oct 9;406(3):235-9. doi: 10.1016/j.neulet.2006.07.037. Epub 2006 Aug 14. Neurosci Lett. 2006. PMID: 16904828
Drugs inducing or aggravating parkinsonism: a review.
Marti-Massó JF, Poza JJ, Lopez de Munain A. Marti-Massó JF, et al. Among authors: lopez de munain a. Therapie. 1996 Sep-Oct;51(5):568-77. Therapie. 1996. PMID: 9138399 Review.
Mitochondrial polymporphisms in Parkinson's Disease.
Otaegui D, Paisán C, Sáenz A, Martí I, Ribate M, Martí-Massó JF, Pérez-Tur J, López de Munain A. Otaegui D, et al. Among authors: lopez de munain a. Neurosci Lett. 2004 Nov 11;370(2-3):171-4. doi: 10.1016/j.neulet.2004.08.012. Neurosci Lett. 2004. PMID: 15488317
357 results