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Daniela Castillo-García

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Impact of SARS-CoV-2 pandemic on the care for patients with lysosomal disorders: The experience of a Mexican pediatric center

2021 Molecular Genetics and Metabolism
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Female child with Fabry disease and two other genetic diseases, spherocytosis, and congenital hypothyroidism, A case report

2021 Molecular Genetics and Metabolism
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Are genotype and biomarkers enough to initiate enzyme replacement therapy in Fabry disease? The value of the biopsy

2020 Molecular Genetics and Metabolism
- Magdalena Cerón-Rodríguez
- Daniela Castillo-García
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Gaucheromas a complication in 2 children despite enzyme replacement therapy

2020 Molecular Genetics and Metabolism
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Mucopolysaccharidosis type II (Hunter syndrome) with multisystem Langerhans cell histiocytosis - A case report of a not described association

2019 Molecular Genetics and Metabolism
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Identification of a novel GLA mutation (V269L) in a Mexican 2-year-old male with Fabry nephropathy: A case report

2019 Molecular Genetics and Metabolism
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