PEDRO
MARTUL TOBIO
Investigador/a en el periodo 1992-2008
AMAIA
VELA DESOJO
PROFESORADO LABORAL INTERINO
Publicaciones en las que colabora con AMAIA VELA DESOJO (12)
2008
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Haploinsufficiency at GCK gene is not a frequent event in MODY2 patients
Clinical Endocrinology, Vol. 68, Núm. 6, pp. 873-878
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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
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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
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Panhypopituitarism: Genetic versus acquired etiological factors
Journal of Pediatric Endocrinology and Metabolism, Vol. 20, Núm. 1, pp. 27-36
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Pubertad precoz
Endocrinología y nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición, Vol. 54, Núm. 5, pp. 259-264
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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
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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
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Obesidad
Anales de Pediatria Continuada, Vol. 4, Núm. 6, pp. 354-360
2005
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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
2004
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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
2002
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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
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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