Martí MJ - Search Results

1

Cerebrospinal fluid levels of coenzyme Q10 are reduced in multiple system atrophy.

Compta Y, Giraldo DM, Muñoz E, Antonelli F, Fernández M, Bravo P, Soto M, Cámara A, Torres F, Martí MJ; Catalan MSA Registry (CMSAR). Compta Y, et al. Among authors: marti mj. Parkinsonism Relat Disord. 2018 Jan;46:16-23. doi: 10.1016/j.parkreldis.2017.10.010. Epub 2017 Oct 20. Parkinsonism Relat Disord. 2018. PMID: 29107645

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

Pure autonomic failure with altered dopamine transporter imaging.

Compta Y, Martí MJ, Paredes P, Tolosa E. Compta Y, et al. Among authors: marti mj. Arch Neurol. 2006 Apr;63(4):604-5. doi: 10.1001/archneur.63.4.604. Arch Neurol. 2006. PMID: 16606777 No abstract available.

5

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

6

Eating-induced facial myoclonic dystonia probably due to a putaminal lesion.

Gaig C, Muñoz E, Valls-Solé J, Martí MJ, Tolosa E. Gaig C, et al. Among authors: marti mj. Mov Disord. 2007 Apr 30;22(6):877-80. doi: 10.1002/mds.21345. Mov Disord. 2007. PMID: 17290449

7

Long lasting pure freezing of gait preceding progressive supranuclear palsy: a clinicopathological study.

Compta Y, Valldeoriola F, Tolosa E, Rey MJ, Martí MJ, Valls-Solé J. Compta Y, et al. Among authors: marti mj. Mov Disord. 2007 Oct 15;22(13):1954-8. doi: 10.1002/mds.21612. Mov Disord. 2007. PMID: 17724746

8

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

9

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

10

5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.

Cruchaga C, Vidal-Taboada JM, Ezquerra M, Lorenzo E, Martinez-Lage P, Blazquez M, Tolosa E; Iberian Atypical Parkinsonism Study Group Researchers; Pastor P. Cruchaga C, et al. Neurobiol Dis. 2009 Feb;33(2):164-70. doi: 10.1016/j.nbd.2008.09.027. Epub 2008 Nov 1. Neurobiol Dis. 2009. PMID: 19022385

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