Laura Papendieck-Gruneiro
B, Argentina
Last Updated: 09/26/2026
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Found 8 publications
Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection.
Journal: Hormone research in paediatrics
Published: May 17, 2017
Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases
Journal: Archivos argentinos de pediatria
Published: May 16, 2017
Differentiated Thyroid Cancer in Children: Prevalence and Predictors in a Large Cohort with Thyroid Nodules Followed Prospectively.
Journal: The Journal of pediatrics
Published: September 30, 2014
Prevalence and etiology of congenital hypothyroidism detected through an argentine neonatal screening program (1997-2010).
Journal: Hormone research in paediatrics
Published: November 30, 2012
New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidism.
Journal: Molecular and cellular endocrinology
Published: July 21, 2012
Severe congenital non-autoimmune hyperthyroidism associated to a mutation in the extracellular domain of thyrotropin receptor gene.
Journal: Arquivos brasileiros de endocrinologia e metabologia
Published: July 12, 2012
Differentiated thyroid carcinoma: presentation and follow-up in children and adolescents.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: December 08, 2011
Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene.
Journal: Clinical endocrinology
Published: October 11, 2011
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Last Updated: 09/26/2026