Results 41 to 50 of about 679,172 (179)
, 2015 PURPOSE: Although a nation-wide salt iodization program on voluntary basis was implemented in 2005, many areas in our country are still characterized by mild iodine deficiency.
Olivieri, A +4 more
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Thyroid dysfunction in patients with childhood-onset medulloblastoma or primitive neuroectodermal tumor [PDF]
Annals of Pediatric Endocrinology & Metabolism, 2018 Purpose We investigated the clinical characteristics of patients who developed thyroid dysfunction and evaluated the risk factors for hypothyroidism following radiotherapy and chemotherapy in pediatric patients with medulloblastoma or primitive ...
Seung Young Jin +11 more
doaj +1 more source
, 2013 Bar chart showing the deference between Permanent and transient congenital hypothyroidism regarding sex.
Osama E. M. Bekhit (428421) +1 more
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MOESM1 of Factors associated with permanent hypothyroidism in infants with congenital hypothyroidism
, 2019 Additional file 1: Table S1. Demographic and auxologic characteristics of participants (preterm vs term group)a. Table S2. Comparison of preterm group vs term groupa. Table S3. Laboratory findings and levothyroxine dose in preterm groupa.
Park, Eun, Yoon, Ju
openaire +1 more source
, 2019 Supplemental data of study: Mutations and phenotypic characteristics in transient and permanent congenital hypothyroidism: an analysis of literature ...
Bin Yu (14464) +4 more
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Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism [PDF]
European Journal of Endocrinology, 2001 OBJECTIVE: It is suggested that iodide organification defects account for 10% of all cases with congenital hypothyroidism (CH). One candidate gene for these defects is the thyroid peroxidase (TPO) gene. DESIGN: Exons 2, 8-10 and 14 of the TPO gene were examined in 30 patients with permanent CH without a family history of CH.
P, Ambrugger +5 more
openaire +2 more sources
Ascites, pleural, and pericardial effusion in primary hypothyroidism: a rare case report
, 2023 Hypothyroidism is caused by a deficiency of thyroid hormones and is a common endocrine disorder worldwide. It can affect nearly every organ, resulting in multiple clinical manifestations. Ascites, pleural effusion, and pericardial effusion, although less
Mogildea, Mihail +4 more
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BMC PediatricsBackground Before the introduction of newborn screening, congenital hypothyroidism was the leading cause of intellectual disability in infants and children.
Yu-En Kao +8 more
doaj +1 more source
A Rare Case of Ipilimumab-induced Reversible Hypophysitis and Permanent Primary Hypothyroidism [PDF]
Cureus, 2019 Ipilimumab is a monoclonal antibody targeting the cytotoxic T-lymphocyte antigen-4 receptor, which was originally approved for the treatment of metastatic melanoma. It is the first immune checkpoint inhibitor to enter clinical practice. Immune toxicity due to ipilimumab causing colitis, hepatitis, and dermatitis are well-described in literature.
Erra, Amani +4 more
openaire +2 more sources
Review of the risks and/or benefits of thyroxine treatment in ‘mild’ subclinical hypothyroidism [PDF]
, 2013 Subclinical hypothyroidism (SCH) is a form of mild thyroid failure and is a commonly encountered condition in clinical practice. It denotes the presence of a raised serum thyroid stimulating hormone (TSH) and normal serum free thyroid hormone ...
Agius, Rachel
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