[HTML][HTML] Prevalence of transient hypothyroidism in children diagnosed with congenital hypothyroidism between 2000 and 2016
S Gmür, D Konrad, R Fingerhut - International Journal of Molecular …, 2023 - mdpi.com
Newborn screening (NBS) for congenital hypothyroidism (CH) was introduced in
Switzerland in 1977, which allowed for the preclinical, biochemical diagnosis. The aim of …
Switzerland in 1977, which allowed for the preclinical, biochemical diagnosis. The aim of …
[HTML][HTML] Diagnosis and Management of Congenital Hypothyroidism: An Updated Overview
S Koohmanaee, A Bakhshi, S Pourkazem… - Journal of …, 2023 - brieflands.com
Context: Hypothyroidism describes an endocrine disorder that occurs when the thyroid
gland cannot secrete adequate thyroid hormones. Congenital hypothyroidism refers to a …
gland cannot secrete adequate thyroid hormones. Congenital hypothyroidism refers to a …
[HTML][HTML] Personalized Management of Malignant and Non-Malignant Ectopic Mediastinal Thyroid: A Proposed 10-Item Algorithm Approach
Simple Summary A large body of multidisciplinary evidence involves the topic of thyroid
cancer (the most common endocrine malignancy). Nevertheless, exceptional findings such …
cancer (the most common endocrine malignancy). Nevertheless, exceptional findings such …
[HTML][HTML] Deleting Cellular Retinoic-Acid-Binding Protein-1 (Crabp1) Gene Causes Adult-Onset Primary Hypothyroidism in Mice
F Najjar, J Nhieu, CW Wei, L Milbauer, L Burmeister… - Endocrines, 2023 - mdpi.com
Adult-onset primary hypothyroidism is commonly caused by iatrogenic or autoimmune
mechanisms; whether other factors might also contribute to adult hypothyroidism is unclear …
mechanisms; whether other factors might also contribute to adult hypothyroidism is unclear …
Therapeutic targeting of TNIK in papillary thyroid carcinoma: a novel approach for tumor growth suppression
R Zhang, Y Yu, Y Yang, M Zhang, X Zhang, Y Chang… - Medical Oncology, 2024 - Springer
Papillary thyroid carcinoma (PTC) is a common endocrine malignancy. The pathology of
PTC is far from clear. As a kinase that can be targeted, the role of TNIK in PTC has not been …
PTC is far from clear. As a kinase that can be targeted, the role of TNIK in PTC has not been …
[HTML][HTML] Normal intellectual ability and hyperprolactinemia as unique clinical manifestations of congenital hypothyroidism: A case report and review of hypotheses
PO Zulfa, M Debbyousha, KW Sucipto… - Narra J, 2023 - ncbi.nlm.nih.gov
Congenital hypothyroidism is the deficiency of thyroid hormone in infants and
hyperprolactinemia is frequently observed. Previously reported cases typically involve …
hyperprolactinemia is frequently observed. Previously reported cases typically involve …
A Computational Approach: The Functional Effects of Thyroid Peroxidase Variants in Thyroid Cancer and Genetic Disorders
A Sobitan, B Gebremedhin, Q Yao, G Xie… - JCO Clinical Cancer …, 2024 - ascopubs.org
PURPOSE Thyroid peroxidase (TPO) is essential for the synthesis of thyroid hormones.
However, specific mutations render TPO antigenic and prone to autoimmune attacks leading …
However, specific mutations render TPO antigenic and prone to autoimmune attacks leading …
[HTML][HTML] Case Report-Multinodular goiter in a patient with Congenital Hypothyroidism and Bannayan-Riley-Ruvalcaba syndrome: the possible synergic role of TPO …
G Vincenzi, IT Petralia, M Abbate, G Tarantola… - Frontiers in …, 2023 - frontiersin.org
We report the case of a paediatric female patient affected by Bannayan-Riley-Ruvalcaba
syndrome (BRRS) and congenital hypothyroidism (CH) with homozygous mutation of the …
syndrome (BRRS) and congenital hypothyroidism (CH) with homozygous mutation of the …
[HTML][HTML] Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report
E Sciarroni, L Montanelli, C Di Cosmo… - Italian Journal of …, 2024 - Springer
Background In this study, we used targeted next-generation sequencing (NGS) to
investigate the genetic basis of congenital hypothyroidism (CH) in a 19-year-old Tunisian …
investigate the genetic basis of congenital hypothyroidism (CH) in a 19-year-old Tunisian …
[HTML][HTML] Evaluation of patients diagnosed with congenital hypothyroidism by newborn screening between 2011–2019 in Diyarbakir, Turkey
This study aimed to determine the incidence of congenital hypothyroidism in Turkey's
Diyarbakir Province and assess the development and growth conditions of people with …
Diyarbakir Province and assess the development and growth conditions of people with …