JAVIER
ELORZ LAMBARRI
Hospital Universitario de Cruces
Barakaldo, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Cruces (12)
2010
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Towards an effective knowledge translation of clinical guidelines and complementary information
Advances in Intelligent and Soft Computing
2009
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Determination of creatine and guanidinoacetate by GC-MS. Study of their stability in urine at different temperatures
Clinical Biochemistry, Vol. 42, Núm. 1-2, pp. 125-128
2008
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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
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Stability of urinary glycosaminoglycans in patients with mucopolysaccharidoses
Clinica Chimica Acta, Vol. 388, Núm. 1-2, pp. 73-77
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The Arginine-creatine pathway is disturbed in children and adolescents with renal transplants
Pediatric Research, Vol. 64, Núm. 2, pp. 218-222
2007
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Arachidonic acid content in adipose tissue is associated with insulin resistance in healthy children
Journal of Pediatric Gastroenterology and Nutrition, Vol. 44, Núm. 1, pp. 77-83
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Essential fatty acid deficiency profile in patients with nephrotic-range proteinuria
Pediatric Nephrology, Vol. 22, Núm. 4, pp. 533-540
2006
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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
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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
2005
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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
2004
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Influence of diet on atherogenic risk in children with renal transplants
Pediatric Nephrology, Vol. 19, Núm. 9, pp. 1039-1045
1996
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Thirteen cystic fibrosis patients, 12 compound heterozygous and one homozygous for the missense mutation G85E: A pancreatic sufficiency/insufficiency mutation with variable clinical presentation
Journal of Medical Genetics, Vol. 33, Núm. 10, pp. 820-822