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Laura Gruñeiro-Papendieck Selected Research

Goiter

10/2007Recurrence 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.
02/2006Three mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the dual oxidase 2 gene responsible for congenital goiter and iodide organification defect.
09/2003Five novel inactivating mutations in the thyroid peroxidase gene responsible for congenital goiter and iodide organification defect.

Articles by Research Topic

Disease

3Goiter
10/2007 - 09/2003
2Hypothyroidism
10/2007 - 01/2004
1Congenital Hypothyroidism (Cretinism)
09/2007

Drug/Important Bio-Agent (IBA)

2ThyroglobulinFDA Link
10/2007 - 09/2007
1OxidoreductasesIBA
02/2006
1beta Subunit Thyrotropin (Thyrotropin-beta)IBA
01/2004
1Iodide Peroxidase (Deiodinase)IBA
09/2003