Congenital hypothyroidism in India: A systematic review and meta-analysis of prevalence, screen positivity rates, and etiology
RP Anne, EA Rahiman - The Lancet Regional Health-Southeast Asia, 2022 - thelancet.com
Background Congenital hypothyroidism (CH) is the leading cause of preventable mental
retardation, which is currently not universally screened in India. Knowledge of the country …
retardation, which is currently not universally screened in India. Knowledge of the country …
[HTML][HTML] Changes of the salivary and serum proteome in canine hypothyroidism
LG González-Arostegui, A Muñoz-Prieto… - Domestic Animal …, 2024 - Elsevier
In this study, changes in salivary and serum proteome of dogs with hypothyroidism were
studied using tandem mass tags (TMT) labelling and liquid chromatography-mass …
studied using tandem mass tags (TMT) labelling and liquid chromatography-mass …
[PDF][PDF] Newborn Screening For Congenital Hypothyroidism Using Cord Blood Tsh And Variations In Cord Blood Tsh With Maternal And Neonatal Factors: Study From …
R Kale, M Bhagwat, C Nayak, K Akhade - Int J Acad Med Pharm, 2022 - academicmed.org
Abstract Background: Congenital Hypothyroidism is most common cause of treatable mental
retardation. Universal screening is now recognised tool for screening in newbornsworld …
retardation. Universal screening is now recognised tool for screening in newbornsworld …
[HTML][HTML] Thyrovigilance for hypothyroidism in India
S Bajaj - Thyroid Research and Practice, 2022 - journals.lww.com
Among endocrine abnormalities, thyroid diseases are the commonest both in India and
worldwide. However, the prevalence of hypothyroidism in India is more than twice as high …
worldwide. However, the prevalence of hypothyroidism in India is more than twice as high …
Newborn Screening in India: A Systematic Review and Meta-Analysis
M Chauhan, A Mahendru, A Bhardwaj… - Available at SSRN … - papers.ssrn.com
Background: In1980s Newborn screening started in India, for early detection of metabolic
disorders in neonates aiming to mitigate severe health outcomes. The prevalence of IEMs …
disorders in neonates aiming to mitigate severe health outcomes. The prevalence of IEMs …
Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in Neonates Presenting with Indirect Hyperbilirubinemia
A Rani, M Khan - Journal of the Dow University of Health Sciences …, 2023 - jduhs.com
Objective: To determine the frequency of glucose-6-phosphate dehydrogenase (G6PD)
deficiency in neonates presenting with indirect hyperbilirubinemia. Methods: A prospective …
deficiency in neonates presenting with indirect hyperbilirubinemia. Methods: A prospective …