Pedro Martul Tobío-rekin lankidetzan egindako argitalpenak (6)

2018

  1. Effect of hydrolyzed infant formula vs conventional formula on risk of type 1 diabetes the TRIGR randomized clinical trial

    JAMA - Journal of the American Medical Association, Vol. 319, Núm. 1, pp. 38-48

2007

  1. Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

    Clinical Endocrinology, Vol. 67, Núm. 4, pp. 538-546

2006

  1. Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress

    Journal of Clinical Endocrinology and Metabolism, Vol. 91, Núm. 5, pp. 1832-1841

2005

  1. Heterogeneity of vitamin D receptor gene association with celiac disease and type 1 diabetes mellitus

    Autoimmunity, Vol. 38, Núm. 6, pp. 439-444

2004

  1. Prospective Population Screening for Celiac Disease: High Prevalence in the First 3 Years of Life

    Journal of Pediatric Gastroenterology and Nutrition, Vol. 39, Núm. 1, pp. 80-84

2002

  1. Molecular analysis of Frasier syndrome: Mutation in the WT1 gene in a girl with gonadal dysgenesis and nephronophthisis

    Journal of Pediatric Endocrinology and Metabolism, Vol. 15, Núm. 7, pp. 1047-1050