Results 21 to 30 of about 1,698 (148)
Hypokalemic thyrotoxic periodic paralysis in a young Serbian male [PDF]
Vojnosanitetski Pregled, 2020 Introduction. Hypokalemic thyrotoxic paralysis is a very rare form of periodic paralysis in Caucasian population. In this population, a more frequent form is familiar hypokalemic periodic paralysis with the same clinical presentation.
Ristić Petar +7 more
doaj +1 more source
Mechanistic Investigation of Curcuma Protection against Oral Submucous Fibrosis
Evidence-Based Complementary and Alternative Medicine, Volume 2022, Issue 1, 2022., 2022 Objective. Oral submucous fibrosis (OSMF) is a chronic, fibrotic disease that affects the oral cavity, showing a high rate of malignant transformation. Curcuma exerts therapeutic potentials in many diseases including OSMF. However, the potential targets and pathways to explain the therapeutic effects of curcuma on OSMF are outside the scope of present ...
Haiyan Peng +6 more
wiley +1 more source
Clinical Case Reports, Volume 9, Issue 3, Page 1055-1059, March 2021., 2021 The same thyroid hormone receptor B gene (THRB) mutation led to thyroid hormone resistance with different clinical manifestations in the kindreds Abstract The same thyroid hormone receptor B gene (THRB) mutation led to thyroid hormone resistance with different clinical manifestations in the kindreds.
Bingkun Huang +7 more
wiley +1 more source
JBMR Plus, Volume 5, Issue 1, January 2021., 2021 ABSTRACT The free hormone hypothesis postulates that only the nonbound fraction (the free fraction) of hormones that otherwise circulate in blood bound to their carrier proteins is able to enter cells and exert biologic effects. In this review, I will examine four hormone groups—vitamin D metabolites (especially 25OHD), thyroid hormones (especially ...
Daniel D Bikle
wiley +1 more source
JCRPE, 2021 Objective:Initial high-dose sodium levothyroxine (Na-LT4) (10-15 μg/kg/day) replacement for primary congenital hypothyroidism (CH) is recommended in guidelines. However, high-dose Na-LT4 risks iatrogenic hyperthyroidism.
Ceren Günbey +5 more
doaj +1 more source
Factitiously Elevated Total Triiodothyronine in a Euthyroid Patient with Multiple Myeloma
Case Reports in Endocrinology, Volume 2021, Issue 1, 2021., 2021 Sporadic reports of factitious elevations of thyroid hormones related to laboratory interference from autoantibodies and multiple myeloma paraproteins have appeared in the literature. Such clinically confusing laboratory results can lead to erroneous diagnoses and inappropriate treatments. We report an additional case of a patient with multiple myeloma
Kaushik Mandal +6 more
wiley +1 more source
Thyroid Dysfunction among Pregnant Women during Different Trimesters of Pregnancy: A Tertiary Care Hospital Based Observational Study [PDF]
National Journal of Laboratory Medicine, 2020 Introduction: Normal thyroid function in pregnancy is important for the health of the mother as well as for the development and growth of the foetus. If pregnancy is associated with any endocrine problems like hypothyroidism, the prospective for maternal
Tripti Saxena +3 more
doaj +1 more source
Effects of Prenatal Stress Exposure on Stress Neurohormonal Axis in Rat Pups of Thyroid Disturbed Mothers [PDF]
Minia Journal of Medical Research, 2020 Thyroid dysfunction during pregnancy is common. Maternal thyroid dysfunction is associated with an increased risk of various adverse maternal and child outcomes, including miscarriage, intrauterine growth retardation, hypertensive disorders, preterm ...
Shimaa Abdel-Latif +4 more
doaj +1 more source
Medicine Science, 2014 The assessment of thyroid function tests for to the diagnose hyperthyroidism (thyrotoxicosis) or hypothyroidism does not constitute a nuisance when the clinical suspicion is strong.
Soner Cander, Ozen Oz Gul, Canan Ersoy
doaj +1 more source
International Journal of Endocrinology, 2019 Objective. Familial dysalbuminemic hyperthyroxinemia (FDH) has now become an established cause for spurious asymptomatic hyperthyroxinemia. Several different codon mutations on albumin gene had been identified.
Hongbing Liu +6 more
doaj +1 more source