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Erratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.
- Published in:
- 2018
- By:
- Publication type:
- Correction Notice
Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson's disease (LARGE-PD), a case of ancestry.
- Published in:
- NPJ Parkinson's Disease, 2017, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41531-017-0020-6
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- Publication type:
- Article
Juvenile‐Onset Huntington's Disease in Peru: A Case Series of 32 Patients.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 2, p. 238, doi. 10.1002/mdc3.13625
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- Publication type:
- Article
Machado Joseph-Disease Is Rare in the Peruvian Population.
- Published in:
- Cerebellum, 2023, v. 22, n. 6, p. 1192, doi. 10.1007/s12311-022-01491-4
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- Publication type:
- Article
Distribution of the CAG Triplet Repeat in ATXN1, ATXN3, and CACNA1A Loci in Peruvian Population.
- Published in:
- Cerebellum, 2020, v. 19, n. 4, p. 527, doi. 10.1007/s12311-020-01129-3
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- Publication type:
- Article
Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.
- Published in:
- Cerebellum, 2020, v. 19, n. 2, p. 208, doi. 10.1007/s12311-019-01098-2
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- Publication type:
- Article
ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.
- Published in:
- Cerebellum, 2019, v. 18, n. 5, p. 841, doi. 10.1007/s12311-019-01057-x
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- Publication type:
- Article
ATXN3, ATXN7, CACNA1A, and RAI1 Genes and Mitochondrial Polymorphism A10398G Did Not Modify Age at Onset in Spinocerebellar Ataxia Type 2 Patients from South America.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Ataxia Rating Scales-Psychometric Profiles, Natural History and Their Application in Clinical Trials.
- Published in:
- Cerebellum, 2012, v. 11, n. 2, p. 488, doi. 10.1007/s12311-011-0316-8
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- Publication type:
- Article
Polyneuropathy in autosomal dominant cerebellar ataxias: phenotype-genotype correlation.
- Published in:
- 1999
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- Publication type:
- journal article
Genotyping strategy for the FMR1 gene: An alternative diagnostic method for the Fragile X syndrome and other trinucleotide expansion diseases.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Estrategia de genotipado del gen FMR1: Mtodo de diagn¢stico alternativo para el S¡ndrome X Frgil y otras enfermedades por expansi¢n de trinucleotidos.
- Published in:
- Revista Medica Herediana, 2013, v. 24, n. 4, p. 269, doi. 10.20453/rmh.2013.269
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- Publication type:
- Article
Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
- Published in:
- Annals of Neurology, 2021, v. 90, n. 3, p. 353, doi. 10.1002/ana.26153
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- Publication type:
- Article
Guillain–Barre syndrome outbreak in Peru: Association with polymorphisms in IL‐17, ICAM1, and CD1.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 10, p. N.PAG, doi. 10.1002/mgg3.960
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- Publication type:
- Article
Genetics and genomics in Peru: Clinical and research perspective.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 6, p. 873, doi. 10.1002/mgg3.533
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- Publication type:
- Article
Parkinson's Disease Gene Screening in Familial Cases from Central and South America.
- Published in:
- Movement Disorders, 2024, v. 39, n. 10, p. 1843, doi. 10.1002/mds.29931
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- Publication type:
- Article
X‐Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.
- Published in:
- Movement Disorders, 2023, v. 38, n. 9, p. 1625, doi. 10.1002/mds.29508
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- Publication type:
- Article
Genome‐Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.
- Published in:
- Movement Disorders, 2021, v. 36, n. 2, p. 434, doi. 10.1002/mds.28353
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- Publication type:
- Article