Laura Gruñeiro‐Papendieck

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

Viviana Varela, Sebastián Esperante, Laura Gruñeiro‐Papendieck et al. · Clinical Chemistry · 2005 · 65 citations · Full text

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

Ana Chiesa, Laura Prieto, Virginia Méndez et al. · Hormone Research in Paediatrics · 2013 · 61 citations

Thyroid Disorders of Neonates Born to Mothers with Graves' Disease

Patricia Papendieck, Ana Chiesa, Laura Prieto et al. · Journal of Pediatric Endocrinology and Metabolism · 2009 · 59 citations

Iodine Deficiency Disorders, Thyroid Disease, Thyroid Abnormalities +13

Congenital hypothyroidism with goitre caused by new mutations in the thyroglobulin gene

Mariela Caputo, Sebastián Esperante, Laura Gruñeiro‐Papendieck et al. · Clinical Endocrinology · 2007 · 52 citations

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

Sebastián Esperante, Laura Gruñeiro‐Papendieck, Ana Chiesa et al. · Human Mutation · 2003 · 52 citations · Full text