Muñoz E - Search Results

1

Tau phosphorylation and kinase activation in familial tauopathy linked to deln296 mutation.

Ferrer I, Pastor P, Rey MJ, Muñoz E, Puig B, Pastor E, Oliva R, Tolosa E. Ferrer I, et al. Among authors: munoz e. Neuropathol Appl Neurobiol. 2003 Feb;29(1):23-34. doi: 10.1046/j.1365-2990.2003.00435.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581337

2

Neurophysiological investigations in patients with head tremor.

Valls-Solé J, Tolosa ES, Nobbe F, Diéguez E, Muñoz E, Sanz P, Valldeoriola F. Valls-Solé J, et al. Among authors: munoz e. Mov Disord. 1997 Jul;12(4):576-84. doi: 10.1002/mds.870120415. Mov Disord. 1997. PMID: 9251077

3

Cervical and facial myoclonus associated with dolichoectasia of the left vertebral artery.

Muñoz EJ, Vila N, Valls-Solé J, Tolosa E. Muñoz EJ, et al. Mov Disord. 1997 Sep;12(5):790-3. doi: 10.1002/mds.870120529. Mov Disord. 1997. PMID: 9380068

4

Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the alpha-synuclein gene in early onset patients.

Muñoz E, Oliva R, Obach V, Martí MJ, Pastor P, Ballesta F, Tolosa E. Muñoz E, et al. Neurosci Lett. 1997 Oct 10;235(1-2):57-60. doi: 10.1016/s0304-3940(97)00710-6. Neurosci Lett. 1997. PMID: 9389595

5

The eye of the tiger sign in cortical-basal ganglionic degeneration.

Molinuevo JL, Muñoz E, Valldeoriola F, Tolosa E. Molinuevo JL, et al. Among authors: munoz e. Mov Disord. 1999 Jan;14(1):169-71. doi: 10.1002/1531-8257(199901)14:1<169::aid-mds1033>3.0.co;2-#. Mov Disord. 1999. PMID: 9918367 No abstract available.

6

Alpha1-antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease.

Muñoz E, Obach V, Oliva R, Martí MJ, Ezquerra M, Pastor P, Ballesta F, Tolosa E. Muñoz E, et al. Neurology. 1999 Jan 15;52(2):297-301. doi: 10.1212/wnl.52.2.297. Neurology. 1999. PMID: 9932947

7

Dopamine receptor D2 intronic polymorphism in patients with Parkinson's disease.

Pastor P, Muñoz E, Obach V, Martí MJ, Blesa R, Oliva R, Tolosa E. Pastor P, et al. Among authors: munoz e. Neurosci Lett. 1999 Oct 8;273(3):151-4. doi: 10.1016/s0304-3940(99)00633-3. Neurosci Lett. 1999. PMID: 10515181

8

Dentatorubropallidoluysian atrophy in a spanish family: a clinical, radiological, pathological, and genetic study.

Muñoz E, Milà M, Sánchez A, Latorre P, Ariza A, Codina M, Ballesta F, Tolosa E. Muñoz E, et al. J Neurol Neurosurg Psychiatry. 1999 Dec;67(6):811-4. doi: 10.1136/jnnp.67.6.811. J Neurol Neurosurg Psychiatry. 1999. PMID: 10567506 Free PMC article.

9

Significant association between the tau gene A0/A0 genotype and Parkinson's disease.

Pastor P, Ezquerra M, Muñoz E, Martí MJ, Blesa R, Tolosa E, Oliva R. Pastor P, et al. Among authors: munoz e. Ann Neurol. 2000 Feb;47(2):242-5. Ann Neurol. 2000. PMID: 10665497

10

A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism.

Muñoz E, Pastor P, Martí MJ, Oliva R, Tolosa E. Muñoz E, et al. Neurosci Lett. 2000 Jul 28;289(1):66-8. doi: 10.1016/s0304-3940(00)01248-9. Neurosci Lett. 2000. PMID: 10899410

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