×
About 186 results

ALLMedicine™ Allan-Herndon-Dudley Syndrome Center

Research & Reviews  93 results

Brain Gene Expression in Systemic Hypothyroidism and Mouse Models of MCT8 Deficiency: T...
https://doi.org/10.1089/thy.2020.0649
Thyroid : Official Journal of the American Thyroid Associ... Morte B, Gil-Ibañez P et. al.

Dec 14th, 2020 - Background: The monocarboxylate transporter 8 (Mct8) protein is a primary thyroxine (T4) and triiodothyronine (T3) (thyroid hormone [TH]) transporter. Mutations of the MCT8-encoding, SLC16A2 gene alter thyroid function and TH metabolism and severe...

Spatiotemporal Changes of Cerebral Monocarboxylate Transporter 8 Expression.
https://doi.org/10.1089/thy.2019.0544
Thyroid : Official Journal of the American Thyroid Associ... Wilpert NM, Krueger M et. al.

Mar 7th, 2020 - Background: Mutations of monocarboxylate transporter 8 (MCT8), a thyroid hormone (TH)-specific transmembrane transporter, cause a severe neurodevelopmental disorder, the Allan-Herndon-Dudley syndrome. In MCT8 deficiency, TH is not able to reach th...

Allan-Herndon-Dudley Syndrome - GeneReviews® - NCBI Bookshelf
https://www.ncbi.nlm.nih.gov/books/n/gene/thctd/

Jan 15th, 2020 - Allan-Herndon-Dudley syndrome (AHDS), an X-linked disorder, is characterized in males by neurologic findings (hypotonia and feeding difficulties in infancy, developmental delay / intellectual disability ranging from mild to profound) and later-ons...

Neural Alterations and Hyperactivity of the Hypothalamic-Pituitary-Thyroid Axis in Oatp...
https://doi.org/10.1089/thy.2019.0320
Thyroid : Official Journal of the American Thyroid Associ... Admati I, Wasserman-Bartov T et. al.

Dec 4th, 2019 - Background: The thyroid hormones (THs) triiodothyronine (T3) and thyroxine (T4) are crucial regulators of brain development and function. Cell-specific transporter proteins facilitate TH uptake and efflux across the cell membrane, and insufficient...

Triac in the treatment of Allan-Herndon-Dudley syndrome.
https://doi.org/10.1016/S2213-8587(19)30217-7
The Lancet. Diabetes & Endocrinology; Bauer AJ

Aug 4th, 2019 - Triac in the treatment of Allan-Herndon-Dudley syndrome.|2019|Bauer AJ,|

see more →

Clinicaltrials.gov  93 results

Brain Gene Expression in Systemic Hypothyroidism and Mouse Models of MCT8 Deficiency: T...
https://doi.org/10.1089/thy.2020.0649
Thyroid : Official Journal of the American Thyroid Associ... Morte B, Gil-Ibañez P et. al.

Dec 14th, 2020 - Background: The monocarboxylate transporter 8 (Mct8) protein is a primary thyroxine (T4) and triiodothyronine (T3) (thyroid hormone [TH]) transporter. Mutations of the MCT8-encoding, SLC16A2 gene alter thyroid function and TH metabolism and severe...

Spatiotemporal Changes of Cerebral Monocarboxylate Transporter 8 Expression.
https://doi.org/10.1089/thy.2019.0544
Thyroid : Official Journal of the American Thyroid Associ... Wilpert NM, Krueger M et. al.

Mar 7th, 2020 - Background: Mutations of monocarboxylate transporter 8 (MCT8), a thyroid hormone (TH)-specific transmembrane transporter, cause a severe neurodevelopmental disorder, the Allan-Herndon-Dudley syndrome. In MCT8 deficiency, TH is not able to reach th...

Allan-Herndon-Dudley Syndrome - GeneReviews® - NCBI Bookshelf
https://www.ncbi.nlm.nih.gov/books/n/gene/thctd/

Jan 15th, 2020 - Allan-Herndon-Dudley syndrome (AHDS), an X-linked disorder, is characterized in males by neurologic findings (hypotonia and feeding difficulties in infancy, developmental delay / intellectual disability ranging from mild to profound) and later-ons...

Neural Alterations and Hyperactivity of the Hypothalamic-Pituitary-Thyroid Axis in Oatp...
https://doi.org/10.1089/thy.2019.0320
Thyroid : Official Journal of the American Thyroid Associ... Admati I, Wasserman-Bartov T et. al.

Dec 4th, 2019 - Background: The thyroid hormones (THs) triiodothyronine (T3) and thyroxine (T4) are crucial regulators of brain development and function. Cell-specific transporter proteins facilitate TH uptake and efflux across the cell membrane, and insufficient...

Triac in the treatment of Allan-Herndon-Dudley syndrome.
https://doi.org/10.1016/S2213-8587(19)30217-7
The Lancet. Diabetes & Endocrinology; Bauer AJ

Aug 4th, 2019 - Triac in the treatment of Allan-Herndon-Dudley syndrome.|2019|Bauer AJ,|

see more →