Showing 1 - 15 results of 15 for search 'Mercedes Serrano', query time: 0.24s Refine Results
  1. 1
    Stroke-Like Episodes in PMM2-CDG: When the Lack of Other Evidence Is the Only Evidence
    by Mercedes Serrano, Mercedes Serrano
    Published 2021-10-01
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    Article
  2. 2
    La sociedad civil y las enfermedades raras
    by Mercedes Serrano
    Published 2018-09-01
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    Article
  3. 3
    El marco jurídico de los datos relativos a la salud en el ámbito de la salud y de la investigación en salud tras la entrada en vigor del Reglamento General de Protección de Datos y de la Ley de Protección de Datos Personales y garantía de los derechos
    by Mª Mercedes Serrano Pérez
    Published 2020-12-01
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    Article
  4. 4
    Apuntes para una nueva cultura de cuidados en salud mental
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    Article
  5. 5
    Plasmatic B-Type Natriuretic Peptide and C-Reactive Protein in Hyperacute Stroke as Markers of Ct-Evidence of Brain Edema
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  6. 6
    Programas de Educación Financiera Implementados en América Latina
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  7. 7
    Cerebrospinal fluid neopterin analysis in neuropediatric patients: establishment of a new cut off-value for the identification of inflammatory-immune mediated processes.
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    Article
  8. 8
    Natural Killer Cell Receptors and Cytotoxic Activity in Phosphomannomutase 2 Deficiency (PMM2-CDG).
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    Article
  9. 9
    Correction: Natural Killer Cell Receptors and Cytotoxic Activity in Phosphomannomutase 2 Deficiency (PMM2-CDG).
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    Article
  10. 10
    Evaluating, Filtering and Clustering Genetic Disease Cohorts Based on Human Phenotype Ontology Data with Cohort Analyzer
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    Article
  11. 11
    Factor XII in PMM2-CDG patients: role of N-glycosylation in the secretion and function of the first element of the contact pathway
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  12. 12
    A quantitative assessment of the evolution of cerebellar syndrome in children with phosphomannomutase-deficiency (PMM2-CDG)
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  13. 13
    <i>CACNA1A</i> Mutations Causing Early Onset Ataxia: Profiling Clinical, Dysmorphic and Structural-Functional Findings
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  14. 14
    Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum
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  15. 15
    Stroke-Like Episodes and Cerebellar Syndrome in Phosphomannomutase Deficiency (PMM2-CDG): Evidence for Hypoglycosylation-Driven Channelopathy
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    Article
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