Ezquerra M - Search Results

1

Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.

Ballesta F, Queralt R, Gómez D, Solsona E, Guitart M, Ezquerra M, Moreno J, Oliva R. Ballesta F, et al. Among authors: ezquerra m. Ann Genet. 1999;42(1):11-5. Ann Genet. 1999. PMID: 10214502

2

Cerebrospinal fluid cytokines in multiple system atrophy: A cross-sectional Catalan MSA registry study.

Compta Y, Dias SP, Giraldo DM, Pérez-Soriano A, Muñoz E, Saura J, Fernández M, Bravo P, Cámara A, Pulido-Salgado M, Painous C, Ríos J, Martí MJ; CMSAR consortium. Compta Y, et al. Parkinsonism Relat Disord. 2019 Aug;65:3-12. doi: 10.1016/j.parkreldis.2019.05.040. Epub 2019 Jun 3. Parkinsonism Relat Disord. 2019. PMID: 31178335

3

The genotype 2/2 of the presenilin-1 polymorphism is decreased in Spanish early-onset Alzheimer's disease.

Ezquerra M, Blesa R, Tolosa E, Lopez Pousa S, Aguilar M, Peña J, Van Broeckhoven C, Ballesta F, Oliva R. Ezquerra M, et al. Neurosci Lett. 1997 May 23;227(3):201-4. doi: 10.1016/s0304-3940(97)00328-5. Neurosci Lett. 1997. PMID: 9185685

4

Low apolipoprotein E epsilon4 allele frequency in the population of Catalonia (Spain) determined by PCR-RFLP and Laser fluorescent sequencer.

Gené M, Moreno P, Ezquerra M, Prat A, Huguet E, Adroer R, Oliva R. Gené M, et al. Among authors: ezquerra m. Eur J Epidemiol. 1997 Oct;13(7):841-3. doi: 10.1023/a:1007389303525. Eur J Epidemiol. 1997. PMID: 9384276

5

Alpha-antichymotrypsin gene polymorphism and risk for Alzheimer's disease in the Spanish population.

Ezquerra M, Blesa R, Tolosa E, Ballesta F, Oliva R. Ezquerra M, et al. Neurosci Lett. 1998 Jan 9;240(2):107-9. doi: 10.1016/s0304-3940(97)00924-5. Neurosci Lett. 1998. PMID: 9486483

6

Apolipoprotein E epsilon 4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers.

Ezquerra M, Ballesta F, Queralt R, Aledo R, Gómez D, Guitart M, Egozcue J, Ascaso C, Oliva R. Ezquerra M, et al. Neurosci Lett. 1998 May 22;248(1):1-4. doi: 10.1016/s0304-3940(98)00251-1. Neurosci Lett. 1998. PMID: 9665649

7

Significant changes in the tau A0 and A3 alleles in progressive supranuclear palsy and improved genotyping by silver detection.

Oliva R, Tolosa E, Ezquerra M, Molinuevo JL, Valldeoriola F, Burguera J, Calopa M, Villa M, Ballesta F. Oliva R, et al. Among authors: ezquerra m. Arch Neurol. 1998 Aug;55(8):1122-4. doi: 10.1001/archneur.55.8.1122. Arch Neurol. 1998. PMID: 9708963

8

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. Among authors: ezquerra m. Neurology. 1999 Jan 15;52(2):297-301. doi: 10.1212/wnl.52.2.297. Neurology. 1999. PMID: 9932947

9

A presenilin 1 mutation (Ser169Pro) associated with early-onset AD and myoclonic seizures.

Ezquerra M, Carnero C, Blesa R, Gelpí JL, Ballesta F, Oliva R. Ezquerra M, et al. Neurology. 1999 Feb;52(3):566-70. doi: 10.1212/wnl.52.3.566. Neurology. 1999. PMID: 10025789

10

Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

Ezquerra M, Pastor P, Valldeoriola F, Molinuevo JL, Blesa R, Tolosa E, Oliva R. Ezquerra M, et al. Neurosci Lett. 1999 Nov 19;275(3):183-6. doi: 10.1016/s0304-3940(99)00738-7. Neurosci Lett. 1999. PMID: 10580705

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