L. Gruñeiro‐Papendieck

发表

Thyroid Disorders of Neonates Born to Mothers with Graves' Disease

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

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

R. González-Sarmiento, H. Targovnik, L. Gruñeiro-Papendieck, 2012, Clinical endocrinology.

Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect

H. Targovnik, S. Esperante, L. Gruñeiro-Papendieck, 2003, Human mutation.

Clinical, biochemical, and molecular findings in Argentinean patients with goitrous congenital hypothyroidism

H. Targovnik, L. Gruñeiro-Papendieck, A. Chiesa, 2010, Endocrine.

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

R. González-Sarmiento, H. Targovnik, L. Gruñeiro-Papendieck, 2007, Clinical endocrinology.

Pediatric Graves' Disease: Outcome and Treatment

J. Heinrich, A. Chiesa, G. Finkielstain, 2003 .

Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection

I. Bergadá, L. Gruñeiro-Papendieck, A. Chiesa, 2017, Hormone Research in Paediatrics.

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 .

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.

H. Targovnik, S. Esperante, L. Gruñeiro-Papendieck, 2006, Clinical chemistry.

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.

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.

Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor beta gene.

R. González-Sarmiento, F. Cassorla, H. Targovnik, 2009, Molecular and cellular probes.

New insights into thyroglobulin gene: Molecular analysis of seven novel mutations associated with goiter and hypothyroidism

K. Lachlan, R. González-Sarmiento, Cintia E. Citterio, 2013, Molecular and Cellular Endocrinology.

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

R. González-Sarmiento, M. Caputo, H. Targovnik, 2010, Clinical endocrinology.

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.

R. González-Sarmiento, M. Caputo, H. Targovnik, 2007, The Journal of endocrinology.

Nocturnal TSH Surge and TRH Test Response in the Evaluation of Thyroid Axis in Hypothalamic Pituitary Disorders in Childhood

J. Heinrich, L. Gruñeiro-Papendieck, A. Chiesa, 1998, Hormone Research in Paediatrics.

Subject Index Vol. 62, 2004

P. Czernichow, B. Ermiş, M. Hashemipour, 2004, Hormone Research in Paediatrics.

Contents Vol. 62, 2004

P. Czernichow, B. Ermiş, M. Hashemipour, 2004, Hormone Research in Paediatrics.