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Serum TSH as a thyroid cancer marker

TOPIC: Thyroid nodules Title: Higher serum thyroid stimulating hormone level in thyroid nodule patients is associated with greater risks of differentiated thyroid cancer and avanced tumor stage. Authors: Haymart MR, Repplinger DJ, Leverson GE, Elson DF, Sippel RS, Jaume JC, & Chen H. Reference: Journal of Clinical Endocrinology & Metabolism 93: 809-814, 2008 Summary Context […]

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Heritable (versus environmental) contribution to determine normal thyroid function pattern

TOPIC: Genetics of hypothalamic-pituitary axis Title: Heritability of serum TSH, free T4 and free T2 concentrations: a study of a large UK twin cohort. Authors: Panicker V, Wilson SG, Spector TD, Brown SJ, Falchi M, Richards JB, Surdulescu GL, Lim EM, Flectcher SJ, & Walsh JP. Reference: Clinical Endocrinology 68: 652-659, 2008 Summary Objective Thyroid […]

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Congenital hypothyroidism

TOPIC: Dyshormonogenesis and congenital hypothyroidism Title: Mutations in the iodotyrosine deiodinase gene and hypothyroidism. Authors: Moreno JC, Klootwijk W, van Toor H, Pinto G, D'Alessandro M, L'ger A, Goudie D, Polak M, Gr'ters A, & Visser TJ. Reference: New England Journal of Medicine 358: 1811-1818, 2008 Summary Context DEHAL1 has been identified as the gene […]

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Something new with Hashimoto’s encephalopathy

TOPIC: Hashimoto's encephalopathy Title: Anti-thyroperoxidase antibodies from patients with Hashimoto's encephalopathy bind to cerebellar astrocytes. Authors: Blanchin S, Coffin C, Viader F, Ruf J, Carayon P et al. Reference: Journal of Neuroimmunology 192: 13-20, 2007 Summary Background Hashimoto's encephalopathy is a rare and controversial neurological disorder, which is responsive to treatment with corticosteroids and associated […]

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New insights into Pendred syndrome

TOPIC: P endrin gene mutation induces poor organification, iodine retention & high deiodinase activity Title: Pendred syndrome in two Galician Families: insights into clinical phenotypes through cellular, genetic and molecular studies. Authors: Palos F, Garcia-Rendueles ME, Araujo-Vilar D, Obregon MJ, Calvo RM et al. Reference: Journal of Clinical Endocrinology & Metabolism 93: 267-277, 2008 Summary […]

Read more »

Recent Posts

Serum TSH as a thyroid cancer marker

TOPIC: Thyroid nodules Title: Higher serum thyroid stimulating hormone level in thyroid nodule patients is associated with greater risks of differentiated thyroid cancer and avanced tumor stage. Authors: Haymart MR, Repplinger DJ, Leverson GE, Elson DF, Sippel RS, Jaume JC, & Chen H. Reference: Journal of Clinical Endocrinology & Metabolism 93: 809-814, 2008 Summary Context […]

Read more »

Heritable (versus environmental) contribution to determine normal thyroid function pattern

TOPIC: Genetics of hypothalamic-pituitary axis Title: Heritability of serum TSH, free T4 and free T2 concentrations: a study of a large UK twin cohort. Authors: Panicker V, Wilson SG, Spector TD, Brown SJ, Falchi M, Richards JB, Surdulescu GL, Lim EM, Flectcher SJ, & Walsh JP. Reference: Clinical Endocrinology 68: 652-659, 2008 Summary Objective Thyroid […]

Read more »

Congenital hypothyroidism

TOPIC: Dyshormonogenesis and congenital hypothyroidism Title: Mutations in the iodotyrosine deiodinase gene and hypothyroidism. Authors: Moreno JC, Klootwijk W, van Toor H, Pinto G, D'Alessandro M, L'ger A, Goudie D, Polak M, Gr'ters A, & Visser TJ. Reference: New England Journal of Medicine 358: 1811-1818, 2008 Summary Context DEHAL1 has been identified as the gene […]

Read more »

Something new with Hashimoto’s encephalopathy

TOPIC: Hashimoto's encephalopathy Title: Anti-thyroperoxidase antibodies from patients with Hashimoto's encephalopathy bind to cerebellar astrocytes. Authors: Blanchin S, Coffin C, Viader F, Ruf J, Carayon P et al. Reference: Journal of Neuroimmunology 192: 13-20, 2007 Summary Background Hashimoto's encephalopathy is a rare and controversial neurological disorder, which is responsive to treatment with corticosteroids and associated […]

Read more »

New insights into Pendred syndrome

TOPIC: P endrin gene mutation induces poor organification, iodine retention & high deiodinase activity Title: Pendred syndrome in two Galician Families: insights into clinical phenotypes through cellular, genetic and molecular studies. Authors: Palos F, Garcia-Rendueles ME, Araujo-Vilar D, Obregon MJ, Calvo RM et al. Reference: Journal of Clinical Endocrinology & Metabolism 93: 267-277, 2008 Summary […]

Read more »