Results 71 to 80 of about 1,447,056 (147)

Maternal Hypothyroxinemia impairs Spatial Learning and Synaptic nature and function in the Offspring [PDF]

, 2008
Neurological deficits in the offspring caused by human maternal hypothyroxinemia are thought to be irreversible. To understand the mechanism responsible for these neurological alterations, we induced maternal hypothyroxinemia in pregnant rats. Behavior
Kalergis, Alexis M., Riedel, C. A., Naranjo, D., Mora, S., Rosenthal, D., Noches, V., Lizana, R., Gianini, A., Porto, M., Pancetti, F., Alarcón, L., Gonzalez, P. A., Opazo, M. C., Mora Gutiérrez, Sergio, Eugenin, E., Kalergis, A. M., Bueno, S. M., Riedel, Claudia A., Azkona Mendoza, Garikoitz, Azkcona, G., Porto, M. P.   +20 more
core   +1 more source

Para-occupational exposure to pesticides, PON1 polymorphisms and hypothyroxinemia during the first half of pregnancy in women living in a Mexican floricultural area

, 2019
Background Adequate maternal thyroxine (T4) concentrations during the first half of pregnancy are fundamental to the embryo’s or fetus’ neural development.
Luisa Torres-Sánchez, Claudia Huesca-Gómez, Jennifer Illian Vázquez-Potisek, Ricardo Gamboa, Leticia Yáñez-Estrada, Susana Bassol-Mayagoitia, Julia Blanco-Muñoz, Martha Patricia Nava, Rebeca Mejía-Saucedo   +8 more
core   +1 more source

Maternal cognitive function during pregnancy in relation to hypo‐ and hyperthyroxinemia [PDF]

, 2019
Objective: To assess a possible relationship between maternal cognitive dysfunction during pregnancy and hypothyroxinemia, adjusted for major confounders.Background: Thyroid dysfunction in general is associated with cognitive dysfunction.
Pop, Victor J., Margreet Meems, Wiersinga, Wilmar M., Broeren, Maarten, Vlad Ormindean, Meems, Margreet, Maarten Broeren, Johan K. Denollet, Wilmar M. Wiersinga, Denollet †, Johan, Andreia Mocan, Bunevicius, Adomas, Mocan, Andreia, Adomas Bunevicius, Victor J. Pop, Ormindean, Vlad   +15 more
core   +1 more source

Hypothyroxinemia Induced by Mild Iodine Deficiency Deregulats Thyroid Proteins during Gestation and Lactation in Dams

, 2013
The main object of the present study was to explore the effect on thyroidal proteins following mild iodine deficiency (ID)-induced maternal hypothyroxinemia during pregnancy and lactation.
Yi Wang, Zhongyan Shan, Hui Min, Wei Wei, Jie Chen, Jing Dong, Yuan Wang, Binbin Song, Qi Xi, Weiping Teng   +9 more
core   +1 more source

Premature Pubarche, Hyperinsulinemia and Hypothyroxinemia: Novel Manifestations of Congenital Portosystemic Shunts (Abernethy Malformation) in Children

, 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, DEMİRCİOĞLU, SERAP, GÜRAN, TÜLAY, HALİLOĞLU, BELMA   +3 more
core   +1 more source

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, Ünüvar, Tolga, Özkan, Pınar, Abacı, Ayhan, Türkmen, Münevver   +4 more
core   +1 more source

Hypothyroxinemia: a subclinical condition affecting neurodevelopment

, 2010
Hypothyroxinemia with low levels of circulating free thyroxine and normal levels of thyrotropin, which is usually caused by iodine deficiency, may affect pregnant women even in apparently iodine-sufficient areas, and it is debated whether it increases ...
Berbel, Pere, Bernal, Juan, Juan Bernal, Pere Berbel   +3 more
core   +1 more source

EP1618 - ECE_2364 - Skin hyperpigmentation as a clinical manifestation of isolated hypothyroxinemia: a case report

European Journal of Endocrinology
Abstract Introduction Isolated hypothyroxinemia is defined as a reduction in free thyroxine levels with normal thyroid-stimulating hormone (TSH) and has long been considered a condition without clear clinical manifestations.
Oleksandra Zavalniuk, Ilona Rudnieva
openaire   +1 more source

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, Michel Polak, Benoit De Sarcus, Isabelle Desguerre, Jeanne Amiel, Melina Morandini, Helton Estrela Ramos, Nathalie Neri, Laurent Mandelbrot, Elodie Tron, Vassili Valayannopoulos, Aurore Carré, Jean Paul Bonnefont, Mireille Castanet, Corinne Floch   +14 more
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PREVENTION OF PLACENTAL INSUFFICIENCY IN PREGNANT WOMEN WITH DIFFUSE GOITER AND HYPOTHYROXINEMIA

, 2019
Objective: To assess the clinical acceptability of prevention of placental insufficiency (PI) by nitric oxide donators (NOD) in pregnant women with diffuse goiter.
M.YA. KAMILOVA, M.A. KHAKNAZAROVA, SH.D. SAYDAKHMADOVA, N.G. RAKHIMOV   +3 more
core   +1 more source