Publikationen in Zusammenarbeit mit Forschern von Instituto Tecnológico y de Estudios Superiores de Monterrey (9)

2019

  1. A 42-year-old woman with untreated growth hormone insensitivity, diabetic retinopathy, and gene sequencing identifies a variant of laron syndrome

    American Journal of Case Reports, Vol. 20, pp. 689-696

2017

  1. Clinical and molecular diagnosis of a cartilage-hair hypoplasia with IGF-1 deficiency

    American Journal of Medical Genetics, Part A, Vol. 173, Núm. 2, pp. 537-540

  2. Experimental approach to IGF-1 therapy in CCl4-induced acute liver damage in healthy controls and mice with partial IGF-1 deficiency

    Journal of Translational Medicine, Vol. 15, Núm. 1

  3. Fanconi Anemia and Laron Syndrome

    American Journal of the Medical Sciences, Vol. 353, Núm. 5, pp. 425-432

  4. IGF-1 modulates gene expression of proteins involved in inflammation, cytoskeleton, and liver architecture

    Journal of Physiology and Biochemistry, Vol. 73, Núm. 2, pp. 245-258

2016

  1. Erratum: Intrauterine growth retardation (IUGR) as a novel condition of insulin-like growth factor-1 (IGF-1) deficiency (Rev Physiol Biochem Pharmacol, 10.1007/112_2015_5001)

    Reviews of Physiology, Biochemistry and Pharmacology

  2. Insulin-like growth factor-1 deficiency and metabolic syndrome

    Journal of Translational Medicine, Vol. 14, Núm. 1

  3. Intrauterine growth retardation (IUGR) as a novel condition of insulin-like growth factor-1 (IGF-1) deficiency

    Reviews of Physiology, Biochemistry and Pharmacology, Vol. 170

2015

  1. Immune monitoring of immunosuppression withdrawal of liver transplant recipients

    Transplant Immunology, Vol. 33, Núm. 2, pp. 110-116