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Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?
- Published in:
- Pediatric Nephrology, 2018, v. 33, n. 11, p. 2095, doi. 10.1007/s00467-018-4006-3
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- Article
Consenso de expertos sobre recomendaciones basadas en evidencia para el diagnóstico, tratamiento y seguimiento de enfermedad de Fabry en pediatría.
- Published in:
- Revista Ciencias de la Salud, 2023, v. 21, n. 3, p. 1, doi. 10.12804/revistas.urosario.edu.co/revsalud/a.12504
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- Article
Enzyme replacement therapy interruption in mucopolysaccharidosis type IVA patients and its impact in different clinical outcomes.
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- Journal of Inherited Metabolic Disease Reports, 2021, v. 58, n. 1, p. 104, doi. 10.1002/jmd2.12192
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- Article
GUÍA PARA EL DIAGNÓSTICO, SEGUIMIENTO Y TRATAMIENTO DE LA ENFERMEDAD DE FABRY.
- Published in:
- Medicina (Buenos Aires), 2013, v. 73, n. 5, p. 482
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- Publication type:
- Article
Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0124987
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- Article