Martí MJ - Search Results

1

Tell-Martí G, Puig-Butille JA, Potrony M, Badenas C, Milà M, Malvehy J, Martí MJ, Ezquerra M, Fernández-Santiago R, Puig S. Tell-Martí G, et al. Among authors: marti mj. Ann Neurol. 2015 Jul;78(1):153-4. doi: 10.1002/ana.24418. Epub 2015 May 25. Ann Neurol. 2015. PMID: 25913870 No abstract available.

2

Further extension of the H1 haplotype associated with progressive supranuclear palsy.

Pastor P, Ezquerra M, Tolosa E, Muñoz E, Martí MJ, Valldeoriola F, Molinuevo JL, Calopa M, Oliva R. Pastor P, et al. Among authors: marti mj. Mov Disord. 2002 May;17(3):550-6. doi: 10.1002/mds.10076. Mov Disord. 2002. PMID: 12112206

3

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.

Gaig C, Ezquerra M, Marti MJ, Muñoz E, Valldeoriola F, Tolosa E. Gaig C, et al. Among authors: marti mj. Arch Neurol. 2006 Mar;63(3):377-82. doi: 10.1001/archneur.63.3.377. Arch Neurol. 2006. PMID: 16533964

4

No evidence of CRHR1 gene involvement in progressive supranuclear palsy.

Campdelacreu J, Gaig C, Ezquerra M, Muñoz E, Martí MJ, Valldeoriola F, Tolosa E. Campdelacreu J, et al. Among authors: marti mj. Neurosci Lett. 2006 Nov 27;409(1):61-4. doi: 10.1016/j.neulet.2006.09.017. Epub 2006 Sep 28. Neurosci Lett. 2006. PMID: 17010515

5

G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies.

Gaig C, Martí MJ, Ezquerra M, Rey MJ, Cardozo A, Tolosa E. Gaig C, et al. Among authors: marti mj. J Neurol Neurosurg Psychiatry. 2007 Jun;78(6):626-8. doi: 10.1136/jnnp.2006.107904. Epub 2007 Jan 8. J Neurol Neurosurg Psychiatry. 2007. PMID: 17210620 Free PMC article.

6

Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.

Gaig C, Ezquerra M, Martí MJ, Valldeoriola F, Muñoz E, Lladó A, Rey MJ, Cardozo A, Molinuevo JL, Tolosa E. Gaig C, et al. Among authors: marti mj. J Neurol Sci. 2008 Jul 15;270(1-2):94-8. doi: 10.1016/j.jns.2008.02.010. Epub 2008 Mar 19. J Neurol Sci. 2008. PMID: 18353371

7

Lack of association of APOE and tau polymorphisms with dementia in Parkinson's disease.

Ezquerra M, Campdelacreu J, Gaig C, Compta Y, Muñoz E, Martí MJ, Valldeoriola F, Tolosa E. Ezquerra M, et al. Among authors: marti mj. Neurosci Lett. 2008 Dec 19;448(1):20-3. doi: 10.1016/j.neulet.2008.10.018. Epub 2008 Oct 10. Neurosci Lett. 2008. PMID: 18930114

8

High cerebrospinal tau levels are associated with the rs242557 tau gene variant and low cerebrospinal β-amyloid in Parkinson disease.

Compta Y, Ezquerra M, Muñoz E, Tolosa E, Valldeoriola F, Rios J, Cámara A, Fernández M, Buongiorno MT, Marti MJ. Compta Y, et al. Among authors: marti mj. Neurosci Lett. 2011 Jan 7;487(2):169-73. doi: 10.1016/j.neulet.2010.10.015. Epub 2010 Oct 15. Neurosci Lett. 2011. PMID: 20951764

9

123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations.

Valldeoriola F, Gaig C, Muxí A, Navales I, Paredes P, Lomeña F, De la Cerda A, Buongiorno M, Ezquerra M, Santacruz P, Martí MJ, Tolosa E. Valldeoriola F, et al. Among authors: marti mj. J Neurol. 2011 Jun;258(6):1126-32. doi: 10.1007/s00415-010-5896-6. Epub 2011 Jan 8. J Neurol. 2011. PMID: 21221623 Free PMC article.

10

Rapidly progressive diffuse Lewy body disease.

Gaig C, Valldeoriola F, Gelpi E, Ezquerra M, Llufriu S, Buongiorno M, Rey MJ, Martí MJ, Graus F, Tolosa E. Gaig C, et al. Among authors: marti mj. Mov Disord. 2011 Jun;26(7):1316-23. doi: 10.1002/mds.23506. Epub 2011 Apr 11. Mov Disord. 2011. PMID: 21484863

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