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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
Dystonia in a Patient with Autosomal-Dominant Progressive External Ophthalmoplegia Type 1 Caused by Mutation in the POLG Gene.
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- Movement Disorders Clinical Practice, 2017, v. 4, n. 2, p. 266, doi. 10.1002/mdc3.12397
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- Publication type:
- Article
Clinical Management of Argentine Hemorrhagic Fever using Ribavirin and Favipiravir, Belgium, 2020.
- Published in:
- 2020
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- Publication type:
- journal article
Neutralizing activity of Sputnik V vaccine sera against SARS-CoV-2 variants.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-24909-9
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- Publication type:
- Article
Clinical and molecular analyses of Beckwith-Wiedemann syndrome: Comparison between spontaneous conception and assisted reproduction techniques.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 10, p. 2740, doi. 10.1002/ajmg.a.37852
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- Publication type:
- Article
Family Environment of Individuals With Oral Clefts in Argentina.
- Published in:
- Cleft Palate Craniofacial Journal, 2005, v. 42, n. 2, p. 185, doi. 10.1597/03-118.1
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- Publication type:
- Article
Different Conformations of Phosphatase and Tensin Homolog, Deleted on Chromosome 10 (PTEN) Protein within the Nucleus and Cytoplasm of Neurons.
- Published in:
- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018857
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- Publication type:
- Article
Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 11, p. 835, doi. 10.1038/sj.ejhg.5201052
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- Publication type:
- Article
One Step Histological Detection and Staining of the PTEN Tumor Suppressor Protein by a Single Strand DNA.
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 2, p. 171, doi. 10.3390/diagnostics11020171
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- Publication type:
- Article
Anp32e/Cpd1 regulates protein phosphatase 2A activity at synapses during synaptogenesis.
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- European Journal of Neuroscience, 2006, v. 23, n. 2, p. 309, doi. 10.1111/j.1460-9568.2005.04555.x
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- Publication type:
- Article
Attitudes toward prenatal diagnosis, termination of pregnancy, and reproduction by parents of children with nonsyndromic oral clefts in Argentina.
- Published in:
- Prenatal Diagnosis, 2003, v. 23, n. 9, p. 722, doi. 10.1002/pd.674
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- Publication type:
- Article
Heterologous Ad26/Ad5 adenovirus-vectored vaccines elicited SARS-CoV-2-specific antibody responses with potent Fc activities.
- Published in:
- Frontiers in Immunology, 2024, p. 01, doi. 10.3389/fimmu.2024.1382619
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- Publication type:
- Article
A new SCARB2 mutation in a patient with progressive myoclonus ataxia without renal failure.
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- Movement Disorders, 2014, v. 29, n. 1, p. 158, doi. 10.1002/mds.25738
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- Publication type:
- Article
A case of severe hearing loss in action myoclonus renal failure syndrome resulting from mutation in SCARB2.
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- Movement Disorders, 2012, v. 27, n. 9, p. 1200, doi. 10.1002/mds.25083
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- Publication type:
- Article
Alpha-synuclein immunoreactivity in minor salivary gland biopsies of Parkinson's disease patients.
- Published in:
- Movement Disorders, 2011, v. 26, n. 1, p. 188, doi. 10.1002/mds.23344
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- Publication type:
- Article