Found: 18
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Low diagnostic accuracy of fragile X tremor/ataxia syndrome diagnostic criteria in late onset ataxia.
- Published in:
- 2019
- By:
- Publication type:
- Letter
Association of variants in the ABCB1, CYP2C19 and CYP2C9 genes for Juvenile Myoclonic Epilepsy.
- Published in:
- Neurological Sciences, 2024, v. 45, n. 4, p. 1635, doi. 10.1007/s10072-023-07124-w
- By:
- Publication type:
- Article
DNA variants in coding region of EFHC1: SNPs do not associate with juvenile myoclonic epilepsy.
- Published in:
- Epilepsia (Series 4), 2009, v. 50, n. 5, p. 1184, doi. 10.1111/j.1528-1167.2008.01762.x
- By:
- Publication type:
- Article
Mutations in EFHC1 cause juvenile myoclonic epilepsy.
- Published in:
- Nature Genetics, 2004, v. 36, n. 8, p. 842, doi. 10.1038/ng1393
- By:
- Publication type:
- Article
Selenium reduces the proapoptotic signaling associated to NF-κB pathway and stimulates glutathione peroxidase activity during excitotoxic damage produced by quinolinate in rat corpus striatum.
- Published in:
- Synapse, 2005, v. 58, n. 4, p. 258, doi. 10.1002/syn.20206
- By:
- Publication type:
- Article
Frecuencia de la apolipoproteína E en una población Nahua.
- Published in:
- Clinical & Translational Investigation / Revista de Investigación Clínica, 2002, v. 54, n. 5, p. 415
- By:
- Publication type:
- Article
TGFBR2 mutation and MTHFR-C677T polymorphism in a Mexican mestizo population with cervico-cerebral artery dissection.
- Published in:
- Journal of Neurology, 2016, v. 263, n. 6, p. 1066, doi. 10.1007/s00415-016-8101-8
- By:
- Publication type:
- Article
Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike waves.
- Published in:
- Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 2, p. 197, doi. 10.1002/mgg3.195
- By:
- Publication type:
- Article
Unraveling the role of relative telomere length and CAG expansion on initial symptoms of juvenile Huntington disease.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 3, p. 612, doi. 10.1111/ene.15644
- By:
- Publication type:
- Article
circRNA Regulates Dopaminergic Synapse, MAPK, and Long-term Depression Pathways in Huntington Disease.
- Published in:
- Molecular Neurobiology, 2021, v. 58, n. 12, p. 6222, doi. 10.1007/s12035-021-02536-1
- By:
- Publication type:
- Article
Espectro de manifestaciones asociadas a X Frágil: descripción clínica y molecular de FMR1 en una familia Mexicana.
- Published in:
- Archivos de Neurociencias, 2018, v. 23, n. 3, p. 54
- By:
- Publication type:
- Article
Espectro de manifestaciones asociadas a X Frágil: descripción clínica y molecular de FMR1 en una familia Mexicana.
- Published in:
- Archivos de Neurociencias, 2018, v. 23, n. 3, p. 54
- By:
- Publication type:
- Article
Estado inflamatorio sistémico y control de las crisis en pacientes con epilepsia mioclónica juvenil: resultados preliminares.
- Published in:
- Archivos de Neurociencias, 2016, v. 21, n. 1, p. 17, doi. 10.31157/archneurosciencesmex.v21i1.107
- By:
- Publication type:
- Article
Correlación entre hallazgos de RM y EEG con el control de crisis en pacientes con epilepsia mioclónica juvenil.
- Published in:
- Archivos de Neurociencias, 2009, v. 14, p. 34
- By:
- Publication type:
- Article
Respuesta a tratamiento en pacientes con epilepsia mioclónica juvenil.
- Published in:
- Archivos de Neurociencias, 2005, v. 10, p. 31
- By:
- Publication type:
- Article
Epilepsia mioclónica juvenil estudio clínico genético.
- Published in:
- Archivos de Neurociencias, 2004, v. 9, p. 33
- By:
- Publication type:
- Article
Homocisteina: un nuevo factor de riesgo para desarrollar enfermedades vasculares.
- Published in:
- Archivos de Neurociencias, 2002, v. 7, n. 1, p. 43
- By:
- Publication type:
- Article
Frecuencia de la mutación C677T en el gen de la metilentetrahidrofolato reductasa en una muestra de la población mexicana.
- Published in:
- Archivos de Neurociencias, 2001, v. 6, p. 16
- By:
- Publication type:
- Article