Neonatal point-of-care testing

T Naghdi, AR Sharifi, RS Tabatabaee, E Azizi… - TrAC Trends in …, 2024 - Elsevier
More than 6,000 infant deaths every day in just the first month of life is a severe alarm for
healthcare systems on the eve of Healthcare 5.0. By providing timely, reliable, yet affordable …

An insight into Indonesia's progress for newborn screening program: What is currently going on

GS Octavius, VA Daleni, YDS Sagala - Heliyon, 2024 - cell.com
Objectives In this literature review, we describe the progress of Indonesia's NBS program
(which is heavily centered on CH screening), its current pilot projects, and what lies ahead …

History of neonatal screening of congenital hypothyroidism in Portugal

MJ Costeira, P Costa, S Roque, I Carvalho… - International Journal of …, 2024 - mdpi.com
Congenital hypothyroidism (CH) leads to growth and development delays and is
preventable with early treatment. Neonatal screening for CH was initiated in Portugal in …

Clinical indicators that influence a clinician's decision to start L-thyroxine treatment in prematurity with transient hypothyroxinemia

A Yilmaz, Y Ozer, N Kaya, AD Cakir, HC Culpan… - Italian journal of …, 2023 - Springer
Background Transient hypothyroxinemia of prematurity (THOP) is defined as a low level of
circulating thyroxine (T4), despite low or normal thyroid-stimulating hormone (TSH) levels …

Congenital hypothyroidism and risk of subsequent autism spectrum disorder and attention‐deficit/hyperactivity disorder in Taiwan

HY Lin, CS Liang, SJ Tsai, JW Hsu… - Psychiatry and …, 2024 - Wiley Online Library
Aim Evidence suggests an association between maternal hypothyroidism and risk of
attention‐deficit/hyperactivity disorder (ADHD) or autism spectrum disorder (ASD) in …

Clinical and molecular study of patients with thyroid dyshormogenesis and variants in the thyroglobulin gene

M Fernandez-Cancio, M Antolín, M Clemente… - Frontiers in …, 2024 - frontiersin.org
Introduction Defects in any thyroid hormone synthesis steps cause thyroid
dyshormonogenesis (THD). THD due to thyroglobulin (TG) gene variants is a cause of …

Utility of repeat testing for congenital hypothyroidism in infants with very low birth weight

SR Rose, CE Blunden, OO Jarrett, K Kaplan… - The Journal of …, 2022 - Elsevier
Objective To assess for possible missed hypothyroidism in infants of very low birth weight
(VLBW) whose initial newborn screening (NBS) was within normal reference range. Study …

A literature review on the redundancy of additional thyroid function tests in neonates of mothers with hypothyroidism

M Deligeorgopoulou, C Kosmeri, V Giapros… - Acta …, 2024 - Wiley Online Library
Aim Newborn thyroid screening tests are carried out during the first days after birth in many
parts of the world. The aim of this review was to assess whether additional thyroid function …

Experiences and challenges with congenital hypothyroidism newborn screening in Indonesia: A national cross-sectional survey

AB Pulungan, HA Puteri, M Faizi, PL Hofman… - International Journal of …, 2024 - mdpi.com
The expansion of newborn screening (NBS) for congenital hypothyroidism (CH) is essential
to reducing the number of preventable intellectual disabilities in children. Because of …

[HTML][HTML] Identification of Intracranial Germ Cell Tumors Based on Facial Photos: Exploratory Study on the Use of Deep Learning for Software Development

Y Li, Y He, Y Liu, B Wang, B Li, X Qiu - Journal of Medical Internet Research, 2025 - jmir.org
Background Primary intracranial germ cell tumors (iGCTs) are highly malignant brain tumors
that predominantly occur in children and adolescents, with an incidence rate ranking third …