Tolosa E - Search Results

1

Ubiquitin-negative mini-pick-like bodies in the dentate gyrus in p301l tauopathy.

Ferrer I, Hernández I, Puig B, Rey MJ, Ezquerra M, Tolosa E, Boada M. Ferrer I, et al. Among authors: tolosa e. J Alzheimers Dis. 2003 Dec;5(6):445-54. doi: 10.3233/jad-2003-5604. J Alzheimers Dis. 2003. PMID: 14757934 Free article.

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: tolosa e. Mov Disord. 2002 May;17(3):550-6. doi: 10.1002/mds.10076. Mov Disord. 2002. PMID: 12112206

3

Presynaptic parkinsonism in multiple system atrophy mimicking Parkinson's disease: a clinicopathological case study.

Berciano J, Valldeoriola F, Ferrer I, Rumià J, Pascual J, Marín C, Rey MJ, Tolosa E. Berciano J, et al. Among authors: tolosa e. Mov Disord. 2002 Jul;17(4):812-6. doi: 10.1002/mds.10190. Mov Disord. 2002. PMID: 12210882

4

Mutational study of the nuclear factor kappa B inducing kinase gene in patients with progressive supranuclear palsy.

Campdelacreu J, Ezquerra M, Muñoz E, Oliva R, Tolosa E. Campdelacreu J, et al. Among authors: tolosa e. Neurosci Lett. 2003 Apr 10;340(2):158-60. doi: 10.1016/s0304-3940(03)00105-8. Neurosci Lett. 2003. PMID: 12668260

5

Severe cerebral white matter involvement in a case of dentatorubropallidoluysian atrophy studied at autopsy.

Muñoz E, Campdelacreu J, Ferrer I, Rey MJ, Cardozo A, Gómez B, Tolosa E. Muñoz E, et al. Among authors: tolosa e. Arch Neurol. 2004 Jun;61(6):946-9. doi: 10.1001/archneur.61.6.946. Arch Neurol. 2004. PMID: 15210537

6

Novel haplotypes in 17q21 are associated with progressive supranuclear palsy.

Pastor P, Ezquerra M, Perez JC, Chakraverty S, Norton J, Racette BA, McKeel D, Perlmutter JS, Tolosa E, Goate AM. Pastor P, et al. Among authors: tolosa e. Ann Neurol. 2004 Aug;56(2):249-58. doi: 10.1002/ana.20178. Ann Neurol. 2004. PMID: 15293277

7

A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome.

Ezquerra M, Campdelacreu J, Muñoz E, Tolosa E, Martí MJ. Ezquerra M, et al. Among authors: tolosa e. Arch Neurol. 2005 Feb;62(2):306-8. doi: 10.1001/archneur.62.2.306. Arch Neurol. 2005. PMID: 15710860

8

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: tolosa e. Arch Neurol. 2006 Mar;63(3):377-82. doi: 10.1001/archneur.63.3.377. Arch Neurol. 2006. PMID: 16533964

9

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: tolosa e. 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

10

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: tolosa e. 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.

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