Search Results - "Galbis Martínez, Liliana"
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Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases
Published in Nefrología (01-03-2023)Get full text
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The importance of the number of antihypertensives in the progression of autosomal dominant polycystic kidney disease
Published in Nefrología (01-05-2021)Get full text
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Multidisciplinary management improves the genetic diagnosis of hereditary kidney diseases in the next generation sequencing (NGS) era
Published in Nefrología (01-01-2024)“…Hereditary kidney diseases (HKD) are a frequent cause of chronic kidney disease, and their diagnosis has increased since the introduction of next generation…”
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El manejo multidisciplinar mejora el diagnóstico genético de las enfermedades renales hereditarias en la era de next generation sequencing (NGS)
Published in Nefrología (01-01-2024)“…Resumen: Antecedentes y objetivo: Las enfermedades renales hereditarias (ERH) son una causa frecuente de enfermedad renal crónica, habiéndose incrementado su…”
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5
Síndrome orofaciodigital tipo i: en el diagnóstico diferencial de la poliquistosis renal autosómica dominante, a próposito de 3 casos
Published in Nefrología (01-03-2023)Get full text
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La importancia del número de antihipertensivos en la progresión de la poliquistosis renal autosómica dominante
Published in Nefrología (01-05-2021)Get full text
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Oral-facio-digital syndrome type I: In the differential diagnosis of autosomic dominant polycystic kidney disease, about three cases
Published in Nefrología (07-08-2021)Get full text
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8
The importance of the number of antihypertensives in the progression of autosomal dominant polycystic kidney disease
Published in Nefrología (01-05-2021)Get full text
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Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications
Published in Scientific reports (15-01-2021)“…Inherited retinal diseases (IRDs), defined by dysfunction or progressive loss of photoreceptors, are disorders characterized by elevated heterogeneity, both at…”
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Author Correction: Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications
Published in Scientific reports (10-05-2021)“…An amendment to this paper has been published and can be accessed via a link at the top of the paper…”
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