FERNANDO
SANTOS RODRIGUEZ
Investigador/a
Hospital de Cruces
Barakaldo, EspañaPublicacións en colaboración con investigadores/as de Hospital de Cruces (18)
2022
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Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study
Nephrology Dialysis Transplantation, Vol. 37, Núm. 12, pp. 2474-2486
2021
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Kidney function in patients with primary distal renal tubular acidosis
Pediatric Nephrology, Vol. 36, Núm. 7, pp. 1931-1935
2020
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Incomplete distal renal tubular acidosis in children
Acta Paediatrica, International Journal of Paediatrics, Vol. 109, Núm. 11, pp. 2243-2250
2019
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Global Variation of Nutritional Status in Children Undergoing Chronic Peritoneal Dialysis: A Longitudinal Study of the International Pediatric Peritoneal Dialysis Network
Scientific Reports, Vol. 9, Núm. 1
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Risk of cardiovascular involvement in pediatric patients with X-linked hypophosphatemia
Pediatric Nephrology, Vol. 34, Núm. 6, pp. 1077-1086
2017
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Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome
PLoS ONE, Vol. 12, Núm. 3
2015
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Cysteamine (Cystagon®) adherence in patients with cystinosis in Spain: Successful in children and a challenge in adolescents and adults
Nephrology Dialysis Transplantation, Vol. 30, Núm. 3, pp. 475-480
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Novel mutations associated with nephrogenic diabetes insipidus. A clinical-genetic study
European Journal of Pediatrics, Vol. 174, Núm. 10, pp. 1373-1385
2013
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Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis
PLoS ONE, Vol. 8, Núm. 1
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Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm
PLoS ONE, Vol. 8, Núm. 9
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RenalTube: A network tool for clinical and genetic diagnosis of primary tubulopathies
European Journal of Pediatrics, Vol. 172, Núm. 6, pp. 775-780
2011
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Growth of kidney-transplanted pediatric patients treated with sirolimus
Pediatric Nephrology, Vol. 26, Núm. 6, pp. 961-966
2010
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Improvement in growth after 1 year of growth hormone therapy in well-nourished infants with growth retardation secondary to chronic renal failure: Results of a multicenter, controlled, randomized, open clinical trial
Clinical Journal of the American Society of Nephrology, Vol. 5, Núm. 7, pp. 1190-1197
2008
2004
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Insuficiencia renal aguda en niños críticamente enfermos. Estudio preliminar
Anales de Pediatria, Vol. 61, Núm. 6, pp. 509-514
1999
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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness
Nature Genetics, Vol. 21, Núm. 1, pp. 84-90
1998
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Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis
Proceedings of the National Academy of Sciences of the United States of America, Vol. 95, Núm. 11, pp. 6337-6342