Allan-Herndon-Dudley syndrome (AHDS)

Known as: Triiodothyronine Resistance, Allan-Herndon-Dudley syndrome, Mental Retardation, X-Linked, With Hypotonia 
A rare, X-linked recessive inherited syndrome caused by mutations in the SLC16A2 (MCT8) gene. It affects exclusively males and is characterized by… (More)
National Institutes of Health

Papers overview

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2015
2015
BACKGROUND Mutations in the thyroid hormone (TH) transporter MCT8 have been identified as the cause for Allan-Herndon-Dudley… (More)
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2015
2015
Allan-Herndon-Dudley syndrome is an X-linked disease caused by mutations in the solute carrier family 16 member 2 (SLC16A2) gene… (More)
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2013
2013
Monocarboxylate transporter 8 (MCT8) is a thyroid hormone (TH)-specific transporter. Mutations in the MCT8 gene are associated… (More)
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2010
2010
Thyroid hormones are known to be essential for growth, development and metabolism. Recently mutations in the SLC16A2 gene coding… (More)
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2008
2008
Mutations in the thyroid monocarboxylate transporter 8 gene (MCT8/SLC16A2) have been reported to result in X-linked mental… (More)
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Review
2007
Review
2007
Thyroid hormone is essential for the proper development and function of the brain. The active form of thyroid hormone is T(3… (More)
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Highly Cited
2007
Highly Cited
2007
Skeletal muscle primarily relies on carbohydrate (CHO) for energy provision during high-intensity exercise. We hypothesized that… (More)
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2006
2006
We report a novel 1 bp deletion (c.1834delC) in the MCT8 gene in a large Brazilian family with Allan-Herndon-Dudley syndrome… (More)
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Highly Cited
2006
Highly Cited
2006
2 www.thelancet.com The global campaign to reduce maternal mortality was launched in February, 1987, when three UN agencies… (More)
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Highly Cited
1998
Highly Cited
1998
Microbiologic reduction of synthetic and geologic Fe31 oxides associated with four Pleistocene-age, Atlantic coastal plain… (More)
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