Found: 19
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Clinical and Molecular Features of First Mexican Friedreich's Ataxia Patients with Compound Heterozygous FXN Mutations.
- Published in:
- 2021
- By:
- Publication type:
- journal article
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
Integrative Genomic–Epigenomic Analysis of Clozapine-Treated Patients with Refractory Psychosis.
- Published in:
- Pharmaceuticals (14248247), 2021, v. 14, n. 2, p. 118, doi. 10.3390/ph14020118
- By:
- Publication type:
- Article
The Phenotypic Spectrum of Spinocerebellar Ataxia Type 19 in a Series of Latin American Patients.
- Published in:
- Cerebellum, 2024, v. 23, n. 4, p. 1727, doi. 10.1007/s12311-023-01654-x
- By:
- Publication type:
- Article
An Exploratory Survey on the Care for Ataxic Patients in the American Continents and the Caribbean.
- Published in:
- Cerebellum, 2023, v. 22, n. 4, p. 708, doi. 10.1007/s12311-022-01442-z
- By:
- Publication type:
- Article
Clozapine Long-Term Treatment Might Reduce Epigenetic Age Through Hypomethylation of Longevity Regulatory Pathways Genes.
- Published in:
- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.870656
- By:
- Publication type:
- Article
Cytogenomic and phenotypic analysis in low-level monosomy 7 mosaicism with non-supernumerary ring chromosome 7.
- Published in:
- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 7, p. 1765, doi. 10.1002/ajmg.a.36503
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- Publication type:
- Article
Clinical and Molecular Findings of Intermediate Allele Carriers in the HTT Gene from the Mexican Mestizo Population.
- Published in:
- Neurodegenerative Diseases, 2022, v. 22, n. 1, p. 34, doi. 10.1159/000526260
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- Publication type:
- Article
Relationship between APOE , PER2 , PER3 and OX2R Genetic Variants and Neuropsychiatric Symptoms in Patients with Alzheimer's Disease.
- Published in:
- International Journal of Environmental Research & Public Health, 2023, v. 20, n. 5, p. 4412, doi. 10.3390/ijerph20054412
- By:
- Publication type:
- Article
Polimorfismos de apoE y reemplazo dopaminérgico en enfermedad de Parkinson.
- Published in:
- Revista Medica del IMSS, 2014, v. 52, n. 1, p. 14
- By:
- Publication type:
- Article
Genetic Testing to Inform Epilepsy Treatment Management From an International Study of Clinical Practice.
- Published in:
- JAMA Neurology, 2022, v. 79, n. 12, p. 1267, doi. 10.1001/jamaneurol.2022.3651
- By:
- Publication type:
- Article
Alcohol intake potentiates clozapine adverse effects associated to CYP1A2*1C in patients with refractory psychosis.
- Published in:
- Drug Development Research, 2021, v. 82, n. 5, p. 685, doi. 10.1002/ddr.21774
- By:
- Publication type:
- Article
ESTUDIO DE ASOCIACIÓN DE VARIANTE GENÉTICA DE BDNF Y LONGITUD TELOMÉRICA EN PACIENTES CON DEMENCIA ALZHEIMER Y CONTROLES.
- Published in:
- Archivos de Neurociencias, 2024, v. 29, p. 55, doi. 10.31157/an.v28iS1.542
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- Publication type:
- Article
Acidemia metilmalónica con deficiencia de Cobalamina C: reporte de dos casos atípicos.
- Published in:
- Archivos de Neurociencias, 2022, v. 27, p. 50
- 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
Síndrome de Pelizaeus Merzbacher: breve revisión de la literatura.
- Published in:
- Archivos de Neurociencias, 2017, v. 22, n. 4, p. 44, doi. 10.31157/archneurosciencesmex.v22i4.167
- By:
- Publication type:
- Article
Protocolo de estudio para una cohorte multicéntrica de pacientes mexicanos con enfermedad de Parkinson para evaluar los determinantes motores, no motores y genéticos sobre la progresión.
- Published in:
- Archivos de Neurociencias, 2012, v. 17, n. 3, p. 159
- By:
- Publication type:
- Article