Differentiated Thyroid Cancer in Children: Prevalence and Predictors in a Large Cohort with Thyroid Nodules Followed Prospectively
Papendieck, Patricia, MD, Gruñeiro-Papendieck, Laura, MD, Venara, Marcela, MD, Acha, Oscar, MD, Cozzani, Hugo, MD, Mateos, Fernanda, MD, Maglio, Silvana, MD, Calcagno, Maria Lujan, Bergada, Ignacio, MD, Chiesa, Ana, MD
Published in The Journal of pediatrics (01.07.2015)
Published in The Journal of pediatrics (01.07.2015)
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Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene
Belforte, Fiorella S., Miras, Mirta B., Olcese, María C., Sobrero, Gabriela, Testa, Graciela, Muñoz, Liliana, Gruñeiro-Papendieck, Laura, Chiesa, Ana, González-Sarmiento, Rogelio, Targovnik, Héctor M., Rivolta, Carina M.
Published in Clinical endocrinology (Oxford) (01.04.2012)
Published in Clinical endocrinology (Oxford) (01.04.2012)
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Predicting hypocalcemia after thyroidectomy in children
Freire, Analía Verónica, MD, Ropelato, María Gabriela, MSc, PhD, Ballerini, María Gabriela, MSc, Acha, Oscar, MD, Bergadá, Ignacio, MD, de Papendieck, Laura Gruñeiro, MD, Chiesa, Ana, MD, PhD
Published in Surgery (01.07.2014)
Published in Surgery (01.07.2014)
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Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect
Varela, Viviana, Rivolta, Carina M, Esperante, Sebastian A, Gruneiro-Papendieck, Laura, Chiesa, Ana, Targovnik, Hector M
Published in Clinical chemistry (Baltimore, Md.) (01.02.2006)
Published in Clinical chemistry (Baltimore, Md.) (01.02.2006)
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Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: haplotype analysis using intragenic thyroglobulin polymorphisms
Caputo, Mariela, Rivolta, Carina M, Gutnisky, Viviana J, Gruñeiro-Papendieck, Laura, Chiesa, Ana, Medeiros-Neto, Geraldo, González-Sarmiento, Rogelio, Targovnik, Héctor M
Published in Journal of endocrinology (01.10.2007)
Published in Journal of endocrinology (01.10.2007)
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Journal Article
Congenital hypothyroidism with goitre caused by new mutations in the thyroglobulin gene
Caputo, Mariela, Rivolta, Carina M., Esperante, Sebastían A., Gruñeiro-Papendieck, Laura, Chiesa, Ana, Pellizas, Claudia G., González-Sarmiento, Rogelio, Targovnik, Héctor M.
Published in Clinical endocrinology (Oxford) (01.09.2007)
Published in Clinical endocrinology (Oxford) (01.09.2007)
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Journal Article
Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7
Machiavelli, Gloria A., Caputo, Mariela, Rivolta, Carina M., Olcese, María C., Gruñeiro-Papendieck, Laura, Chiesa, Ana, González-Sarmiento, Rogelio, Targovnik, Héctor M.
Published in Clinical endocrinology (Oxford) (01.01.2010)
Published in Clinical endocrinology (Oxford) (01.01.2010)
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Differentiated thyroid carcinoma: presentation and follow-up in children and adolescents
Papendieck, Patricia, Gruñeiro-Papendieck, Laura, Venara, Marcela, Acha, Oscar, Maglio, Silvana, Bergadá, Ignacio, Chiesa, Ana
Published in Journal of Pediatric Endocrinology and Metabolism (2011)
Published in Journal of Pediatric Endocrinology and Metabolism (2011)
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Journal Article
Two compound heterozygous mutations (c.215delA/c.2422T→C and c.387delC/c.1159G→A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect
Rivolta, Carina M., Louis-Tisserand, Mariana, Varela, Viviana, Gruñeiro-Papendieck, Laura, Chiesa, Ana, González-Sarmiento, Rogelio, Targovnik, Héctor M.
Published in Clinical endocrinology (Oxford) (01.08.2007)
Published in Clinical endocrinology (Oxford) (01.08.2007)
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Journal Article
Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect
Rivolta, Carina M., Esperante, Sebastián A., Gruñeiro-Papendieck, Laura, Chiesa, Ana, Moya, Christian M., Domené, Sabina, Varela, Viviana, Targovnik, Héctor M.
Published in Human mutation (01.09.2003)
Published in Human mutation (01.09.2003)
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Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection
Braslavsky, Débora, Méndez, Maria Virginia, Prieto, Laura, Keselman, Ana, Enacan, Rosa, Gruñeiro-Papendieck, Laura, Jullien, Nicolas, Savenau, Alexandru, Reynaud, Rachel, Brue, Thierry, Bergadá, Ignacio, Chiesa, Ana
Published in Hormone research in paediatrics (01.01.2017)
Published in Hormone research in paediatrics (01.01.2017)
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Journal Article
Prevalence and Etiology of Congenital Hypothyroidism Detected through an Argentine Neonatal Screening Program (1997-2010)
Chiesa, Ana, Prieto, Laura, Mendez, Virginia, Papendieck, Patricia, Calcagno, María de Luján, Gruñeiro-Papendieck, Laura
Published in Hormone research in paediatrics (01.01.2013)
Published in Hormone research in paediatrics (01.01.2013)
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Journal Article
New insights into thyroglobulin gene: Molecular analysis of seven novel mutations associated with goiter and hypothyroidism
Citterio, Cintia E., Machiavelli, Gloria A., Miras, Mirta B., Gruñeiro-Papendieck, Laura, Lachlan, Katherine, Sobrero, Gabriela, Chiesa, Ana, Walker, Joanna, Muñoz, Liliana, Testa, Graciela, Belforte, Fiorella S., González-Sarmiento, Rogelio, Rivolta, Carina M., Targovnik, Héctor M.
Published in Molecular and cellular endocrinology (30.01.2013)
Published in Molecular and cellular endocrinology (30.01.2013)
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Journal Article
Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases
Enacán, Rosa E, Masnata, María E, Belforte, Fiorella, Papendieck, Patricia, Olcese, María C, Siffo, Sofía, Gruñeiro-Papendieck, Laura, Targovnik, Héctor, Rivolta, Carina M, Chiesa, Ana E
Published in Archivos argentinos de pediatría (01.06.2017)
Published in Archivos argentinos de pediatría (01.06.2017)
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Journal Article
Thyroid Disorders of Neonates Born to Mothers with Graves' Disease
Papendieck, P., Chiesa, A., Prieto, L., Gruñeiro-Papendieck, L.
Published in Journal of Pediatric Endocrinology and Metabolism (01.06.2009)
Published in Journal of Pediatric Endocrinology and Metabolism (01.06.2009)
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Journal Article
Variable clinical presentation and outcome in pediatric patients with resistance to thyroid hormone (RTH)
Chiesa, Ana, Olcese, Maria Cecilia, Papendieck, Patricia, Martinez, Alicia, Vieites, Ana, Bengolea, Sonia, Targovnik, Héctor Manuel, Rivolta, Carina Maria, Gruñeiro-Papendieck, Laura
Published in Endocrine (01.02.2012)
Published in Endocrine (01.02.2012)
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Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor β gene
Rivolta, Carina M., Olcese, María C., Belforte, Fiorella S., Chiesa, Ana, Gruñeiro-Papendieck, Laura, Iorcansky, Sonia, Herzovich, Viviana, Cassorla, Fernando, Gauna, Alicia, Gonzalez-Sarmiento, Rogelio, Targovnik, Héctor M.
Published in Molecular and cellular probes (01.06.2009)
Published in Molecular and cellular probes (01.06.2009)
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