Results 51 to 60 of about 64,440 (255)
Association between thymic hyperplasia and serum calcium level in Graves’ disease
BMC Endocrine DisordersBackground Graves' disease increases bone resorption in hyperthyroidism, leading to elevated serum calcium levels and a negative bone balance. Thymic hyperplasia is observed in some Graves' disease patients.
Jing Zeng, Lan Li, Dong Wei
doaj +1 more source
Клиническая и экспериментальная тиреоидология, 2011 The aim of the study was to estimate a level of thyrotropin-receptor antibodies (TRAb), some cytokines (TNF-α, IL-8, IL-10) in Graves' disease patients with chronic heart failure (CHF) and to reveal prognostic factors of CHF.89 patients with Graves ...
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Peripheral Neutrophil Activation and Extracellular Trap Formation in Amyotrophic Lateral Sclerosis
Annals of Clinical and Translational Neurology, EarlyView.Markers of neutrophil activation are increased in plasma during ALS, and markers of NET formation associate with ALS survival. ABSTRACT Objectives Peripheral neutrophil levels in amyotrophic lateral sclerosis (ALS) inversely correlate with survival, suggesting a role for neutrophils in disease progression.
Lillia A. Baird +9 more
wiley +1 more source
Graves’ Disease and Diagnostic Approaches
Endocrinology Research and Practice, 2007 Although thyroid stimulating hormone receptor antibody (TSH-Rab) is pathogonomonic for Graves’ disease, antibodies against thyroglobulin, thyroperoxidase can also be detected in serum of patients. Many authors propose that ophtalmopathy and/or dermopathy
Melek Eda Ertörer +4 more
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Effects of Radioiodine Therapy on the Natural History of Graves' Ophtalmopathy
Клиническая и экспериментальная тиреоидология, 2007 21 patients with Graves’ disease and Graves’ ophthalmopathy (GO) received radioiodine treatment (RIT). Before 131-I therapy in all patients GO were non-active and no severe.
doaj +1 more source
, 2014 Osteopoikilosis is an uncommon hereditary dysplasia of skeleton characterized by small sclerotic foci clustered mainly in periarticular osseus regions. The radiographic pattern is pathognomonic.
Irena Zimmermann-Górska
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A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
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Treatment of Graves' disease in patients who smoke: a rapid re-view for patient decision aid (update) [PDF]
, 2022 Hovedbudskap Graves’ er en autoimmun sykdom og den vanligste årsaken til høyt stoffskifte hos yngre personer. Ved Graves’ sykdom danner immunforsvaret antistoffer som stimulerer skjoldbruskkjertelen til økt produksjon av hormonet tyroksin. Symptombildet
Klem, Hanna Eikås, Holtet Evensen, Line
core
A Two‐Stage Questionnaire and Actigraphy Screening for iRBD in a Multicenter Retrospective Cohort
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Isolated rapid‐eye‐movement sleep behavior disorder is a prodromal marker of synucleinopathies. However, most cases remain undiagnosed due to the insufficient predictive value of questionnaires and limited access to confirmatory video‐polysomnography. We assessed a two‐stage screening strategy combining a brief questionnaire on rapid‐
Caleb A. Massimi +17 more
wiley +1 more source
Endocrinology Research and Practice, 2022 In this study, we investigated Thyrotropin Receptor Antibody (TRab) levels in Hashimoto and Graves' diseases. A total of 189 patients and 25 controls were assessed, retrospectively.
Demet Çorapçıoğlu +8 more
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