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

Author:

Chiesa Ana,Rivolta Carina M.,Targovnik Héctor M.,Gruñeiro-Papendieck Laura

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference48 articles.

1. A. Grüters, H. Biebermann, H. Krude, Neonatal thyroid disorders. Horm. Res. 59(suppl 1), 24–29 (2003)

2. A. Grüters, R. Finke, H. Krude, H. Meinhold, Etiological grouping of permanent congenital hypothyrroidism with thyroid gland in situ. Horm. Res. 41, 3–9 (1994)

3. V. Pendred, Deaf-mutism and goiter. Lancet 2, 532 (1896)

4. W. Osler, Sporadic cretinism in America Trans Congress. Am. Physicians Surg. 4, 169–206 (1897)

5. J. Stanbury, A. Hedge, A study of a family of goitrous cretins. J. Clin. Endocrinol. Metab. 10, 1471–1475 (1950)

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1. Long-Term Outcome of Patients with TPO Mutations;Journal of Clinical Medicine;2021-08-30

2. Large thyroid cyst in a patient with congenital hypothyroidism;Arquivos Brasileiros de Endocrinologia & Metabologia;2014-12

3. Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes;Clinical Endocrinology;2014-05-19

4. Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene;Journal of Pediatric Endocrinology and Metabolism;2013-01-01

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