Results 81 to 90 of about 2,033 (194)
Frontiers in Endocrinology, 2019 Hypothyroidism has been reported to improve survival in cancer patients but only recently has the putative mechanism been identified as a receptor for thyroxine and tri-iodothyronine on integrin αvβ3.
Aleck Hercbergs
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, 2015 Congenital portosystemic shunt (CPSS) is persistence of an anomalous embryological connection of the portal vein with a large vein of the vena cava system.
BEREKET, ABDULLAH +3 more
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Siriraj Medical JournalBackground: Thyroid hormone is essential for preterm infant development, particularly neurological. Understanding thyroid disorder prevalence and function test characteristics enables proper interpretation and risk identification.
Pichaya Vathanasakpuban +4 more
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, 2021 Isolated hypothyroxinemia (IH) unfavorably affects reproduction. This study aimed to evaluate retrospectively if any routinely measured clinical/laboratory parameters are associated with IH among women of childbearing age hospitalized in the endocrine ...
Małgorzata Karbownik-Lewińska +2 more
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Hypothyroxinemia in a newborn with galactosemia [PDF]
, 2007 Galaktoz ve metabolitleri karaciğer, beyin, lens ve böbrek için toksik olup, ovarium gelişimini de bozabildiği gibi tiroid fonksiyonlarını da etkileyebilmektedir.
Öztürk, Yeşim +4 more
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Obstetric controversies in thyroidology
Indian Journal of Endocrinology and Metabolism, 2013 It is well known that thyroid disorders commonly affect women. The care of pregnant women affected by thyroid disease is an important clinical challenge for endocrinologists. Hypothyroidism is the commonest problem, and maternal hypothyroxinemia has been
Ambika Gopalakrishnan Unnikrishnan +2 more
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Low maternal iodine intake and early pregnancy hypothyroxinemia: Possible repercussions for children
Indian Journal of Endocrinology and Metabolism, 2014 Objective: Recent studies have shown that early pregnancy hypothyroxinemia (lower free thyroxin [FT 4 ] and normal thyroid stimulating hormone [TSH] concentration) has deleterious effects on neuro-intellectual development of children.
Shan Elahi, Saeed Ahmad Nagra
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Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal care
, 2011 ContextMonocarboxylate transporter 8 (MCT8 or SLC16A2) mutations cause X-linked Allan–Herndon–Dudley syndrome. Heterozygous females are usually asymptomatic, but pregnancy may modify thyroid function and MCT8 is expressed in the placenta, suggesting that
Albane Simon +14 more
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Indications for treatment of subclinical hypothyroidism and isolated hypothyroxinaemia in pregnancy
, 2020 Thyroid hormones are essential for maintaining a pregnancy and optimal fetal neurological development. Pregnancy places additional demands on the thyroid axis and around 5% of women who have their thyroid function checked during gestation will have ...
Lazarus, John H. +5 more
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Animal Models and Experimental Medicine, Volume 7, Issue 6, Page ii-viii, December 2024.
wiley +1 more source