P. Papendieck

发表

Differentiated Thyroid Cancer in Children: Prevalence and Predictors in a Large Cohort with Thyroid Nodules Followed Prospectively.

I. Bergadá, L. Gruñeiro-Papendieck, A. Chiesa, 2015, The Journal of pediatrics.

Differentiated thyroid carcinoma: presentation and follow-up in children and adolescents

I. Bergadá, L. Gruñeiro-Papendieck, A. Chiesa, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

Variable clinical presentation and outcome in pediatric patients with resistance to thyroid hormone (RTH)

H. Targovnik, L. Gruñeiro-Papendieck, A. Chiesa, 2012, Endocrine.

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

R. González-Sarmiento, Cintia E. Citterio, J. Weill, 2017, Molecular and Cellular Endocrinology.

Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect

Cintia E. Citterio, F. Savagner, A. Chiesa, 2022, International journal of molecular sciences.

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

R. González-Sarmiento, H. Targovnik, A. Chiesa, 2022, Endocrine.

Association of Distal Deletion of the Short arm of Chromosome 9 with 46,XY Disorder of Sex Development and Gonadoblastoma

M. Venara, P. Papendieck, A. Laudicina, 2015 .

Thyroid Disorders of Neonates Born to Mothers with Graves' Disease

L. Gruñeiro-Papendieck, A. Chiesa, L. Prieto, 2009, Journal of pediatric endocrinology & metabolism : JPEM.

Biallelic Stop Codon Mutations (p.F353Pfs*36/p.Y425X) in DUOX2 Gene Associated with Transient Congenital Hypothyroidism: Report of a Family and Literature Review

H. Targovnik, L. Gruñeiro-Papendieck, A. Chiesa, 2016 .

Prevalence and Etiology of Congenital Hypothyroidism Detected through an Argentine Neonatal Screening Program (1997-2010)

L. Gruñeiro-Papendieck, A. Chiesa, M. Calcagno, 2013, Hormone Research in Paediatrics.

An intramolecular ionic interaction linking defective sodium/iodide symporter transport to the plasma membrane and dyshormonogenic congenital hypothyroidism.

A. Chiesa, J. Nicola, A. M. Masini-Repiso, 2021, Thyroid : official journal of the American Thyroid Association.

[Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases].

H. Targovnik, L. Gruñeiro-Papendieck, A. Chiesa, 2017, Archivos argentinos de pediatria.

Novel Sodium/Iodide Symporter Compound Heterozygous Pathogenic Variants Causing Dyshormonogenic Congenital Hypothyroidism.

A. Chiesa, J. Nicola, Mariano Martín, 2019, Thyroid : official journal of the American Thyroid Association.

Improving safety in paediatric thyroidectomy by PTH measurements

I. Bergadá, A. Chiesa, M. Ropelato, 2021, Clinical endocrinology.

Targeted Next-Generation Sequencing of Congenital Targeted Next-Generation Sequencing of Congenital Hypothyroidism-causative Genes Reveals Unexpected Hypothyroidism-causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Thyroglobulin Gene Variants in Patient

Cintia E. Citterio, J. Nicola, Mariano Martín, 2022 .