Page last updated: 2024-11-06

thyroxine and alpha-Galactosidase A Deficiency

thyroxine has been researched along with alpha-Galactosidase A Deficiency in 2 studies

Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.

Research Excerpts

ExcerptRelevanceReference
"Subclinical hypothyroidism is a common finding in patients with Anderson-Fabry disease, showing an excess prevalence as compared to the normal population."1.33High prevalence of subclinical hypothyroidism in patients with Anderson-Fabry disease. ( Födinger, M; Gessl, A; Hauser, AC; Lorenz, M; Sunder-Plassmann, G; Voigtländer, T, 2005)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (50.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Faggiano, A1
Severino, R1
Ramundo, V1
Russo, R1
Vuolo, L1
Del Prete, M1
Marciello, F1
Lombardi, G1
Cianciaruso, B1
Colao, A1
Pisani, A1
Hauser, AC1
Gessl, A1
Lorenz, M1
Voigtländer, T1
Födinger, M1
Sunder-Plassmann, G1

Other Studies

2 other studies available for thyroxine and alpha-Galactosidase A Deficiency

ArticleYear
Thyroid function in Fabry disease before and after enzyme replacement therapy.
    Minerva endocrinologica, 2011, Volume: 36, Issue:1

    Topics: Adult; Algorithms; alpha-Galactosidase; Biomarkers; Case-Control Studies; Enzyme Replacement Therapy

2011
High prevalence of subclinical hypothyroidism in patients with Anderson-Fabry disease.
    Journal of inherited metabolic disease, 2005, Volume: 28, Issue:5

    Topics: Adult; Fabry Disease; Female; Humans; Hypothyroidism; Kidney Diseases; Lysosomal Storage Diseases; M

2005