Argitalpenak (37) JUAN RODRIGUEZ SORIANO argitalpenak

2011

  1. Methylation cycle, arginine-creatine pathway and asymmetric dimethylarginine in paediatric renal transplant

    Nephrology Dialysis Transplantation, Vol. 26, Núm. 1, pp. 328-336

2008

  1. Fatty acid deficiency profile in children with food allergy managed with elimination diets

    Acta Paediatrica, International Journal of Paediatrics, Vol. 97, Núm. 11, pp. 1572-1576

  2. Hyperchloremia

    Practical Algorithms in Pediatric Nephrology (S. Karger AG), pp. 78-79

  3. Hypernatremia

    Practical Algorithms in Pediatric Nephrology (S. Karger AG), pp. 74-75

  4. Hypokalemia

    Practical Algorithms in Pediatric Nephrology (S. Karger AG), pp. 80-81

  5. Hyponatremia

    Practical Algorithms in Pediatric Nephrology (S. Karger AG), pp. 72-73

  6. The Arginine-creatine pathway is disturbed in children and adolescents with renal transplants

    Pediatric Research, Vol. 64, Núm. 2, pp. 218-222

2007

  1. Essential fatty acid deficiency profile in patients with nephrotic-range proteinuria

    Pediatric Nephrology, Vol. 22, Núm. 4, pp. 533-540

2006

  1. An analysis of renal tubular acidosis by the Stewart method

    Pediatric Nephrology, Vol. 21, Núm. 2, pp. 206-211

  2. Autosomal dominant pseudohypoaldosteronism type 1: Mechanisms, evidence for neonatal lethality, and phenotypic expression in adults

    Journal of the American Society of Nephrology, Vol. 17, Núm. 5, pp. 1429-1436

  3. Effect of docosahexaenoic acid administration on plasma lipid profile and metabolic parameters of children with methylmalonic acidaemia

    Journal of Inherited Metabolic Disease, Vol. 29, Núm. 1, pp. 58-63

  4. Ensayo aleatorizado ciego-sencillo sobre los efectos de las vitaminas C y E en la hipercolesterolemia familiar

    Anales de Pediatria, Vol. 65, Núm. 2, pp. 101-107

  5. Fatty acid composition of skeletal muscle and adipose tissue in Spanish infants and children

    British Journal of Nutrition, Vol. 95, Núm. 1, pp. 168-173

  6. Inherited Renal Tubulopathies Associated With Metabolic Alkalosis: Effects on Blood Pressure

    Seminars in Nephrology, Vol. 26, Núm. 6, pp. 422-433

  7. Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement

    American Journal of Human Genetics, Vol. 79, Núm. 5, pp. 949-957

  8. Osteogenesis imperfecta: Anthropometric, skeletal and mineral metabolic effects of long-term intravenous pamidronate therapy

    Acta Paediatrica, International Journal of Paediatrics, Vol. 95, Núm. 3, pp. 332-339

2005

  1. A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain

    Pediatric Nephrology, Vol. 20, Núm. 7, pp. 891-896

  2. Abnormalities in plasma fatty acid composition in human immunodeficiency virus-infected children treated with protease inhibitors

    Acta Paediatrica, International Journal of Paediatrics, Vol. 94, Núm. 6, pp. 672-677

  3. Bone mineral density and bone turnover in patients with Bartter syndrome

    Pediatric Nephrology, Vol. 20, Núm. 8, pp. 1120-1125

  4. Long-term renal follow-up of extremely low birth weight infants

    Pediatric Nephrology, Vol. 20, Núm. 5, pp. 579-584