Publicaciones en las que colabora con PEDRO MARTUL TOBIO (24)

2013

  1. Lessons from the Hvidoere International Study Group on childhood diabetes: Be dogmatic about outcome and flexible in approach

    Pediatric Diabetes, Vol. 14, Núm. 7, pp. 473-480

2008

  1. Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients

    Clinical Endocrinology, Vol. 68, Núm. 6, pp. 873-878

  2. The exon 3-deleted/full-length growth hormone receptor polymorphism does not influence the effect of puberty or growth hormone therapy on glucose homeostasis in short non-growth hormone-deficient small-for-gestational-age children: Results from a two-year controlled prospective study

    Journal of Clinical Endocrinology and Metabolism, Vol. 93, Núm. 7, pp. 2709-2715

2007

  1. Monitorización continua de la glucosa en la edad pediátrica: indicaciones y aplicación clínica de los resultados

    Avances en diabetología, Vol. 23, Núm. 4, pp. 282-287

  2. 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

  3. Panhypopituitarism: Genetic versus acquired etiological factors

    Journal of Pediatric Endocrinology and Metabolism, Vol. 20, Núm. 1, pp. 27-36

  4. Pubertad precoz

    Endocrinología y nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición, Vol. 54, Núm. 5, pp. 259-264

  5. Virilización en una niña por contacto inadvertido con testosterona tópica

    Endocrinología y nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición, Vol. 54, Núm. 2, pp. 122-124

2006

  1. Children born small for gestational age (SGA) who fail to achieve catch up growth by 2-8 years of age are short from infancy to adulthood: Data from a cross-sectional study of 486 Spanish children

    Pediatric Endocrinology Reviews, Vol. 4, Núm. 1, pp. 15-27

  2. Exon 3-deleted/full-length growth hormone receptor polymorphism genotype frequencies in Spanish short small-for-gestational-age (SGA) children and adolescents (n = 247) and in an adult control population (n = 289) show increased fl/fl in short SGA

    Journal of Clinical Endocrinology and Metabolism, Vol. 91, Núm. 12, pp. 5038-5043

  3. 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

  4. Obesidad

    Anales de Pediatria Continuada, Vol. 4, Núm. 6, pp. 354-360

2005

  1. Circulating non-22 kDa growth hormone isoforms after a repeated GHRH stimulus in normal subjects

    Growth Hormone and IGF Research, Vol. 15, Núm. 2, pp. 123-129

  2. 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. Dual growth hormone (GH) response to repeated GH releasing hormone stimulus in children and adults

    Journal of Pediatric Endocrinology and Metabolism, Vol. 17, Núm. 5, pp. 743-748

  2. 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. Longitudinal study of the pubertal growth spurt in children born small for gestational age without postnatal catch-up growth

    Journal of Pediatric Endocrinology and Metabolism, Vol. 15, Núm. 4, pp. 381-388

  2. 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

2001

  1. Molecular analysis of hereditary hyperferritinemia-cataract syndrome in a large Basque family

    Journal of Pediatric Endocrinology and Metabolism, Vol. 14, Núm. 3, pp. 295-300

1996

  1. Renal tubular handling of potassium in children with insulin-dependent diabetes mellitus

    Pediatric Nephrology, Vol. 10, Núm. 1, pp. 1-6