Results 111 to 120 of about 25,566 (257)

Magnitude and its associated factors of neonatal jaundice among neonates admitted to the neonatal intensive care unit of Dessie Town public hospitals, Amhara region, Ethiopia, 2020: a multicenter cross-sectional study

Frontiers in Pediatrics
BackgroundNeonatal jaundice is a prevalent illness affecting approximately 60%–80% of newborns. In severe cases, it can result in severe neurological distress.
Mohammed Tessema, Hussen Mekonnen, Tsion Alemu, Yohannes Godie, Wegayehu Zeneb Teklehaimanot, Leweyehu Alemaw Mengstie   +5 more
doaj   +1 more source

A Review of Breath Sensing for Disease Monitoring and Diagnosis: Breathomics, Artificial Intelligence, and Nanomaterials for the Future of Medicine

Advanced Sensor Research, Volume 5, Issue 7, July 2026.
Breathomics is established as a non‐invasive diagnostic strategy by combining volatile organic compound biomarkers, nanomaterial‐based sensor arrays, and AI‐driven classification. Key diseases, sensing materials, and analytical challenges are critically compared, revealing how portable, data‐enabled breath platforms are moving toward clinically useful ...
Anesu Nyabadza, Mayur Makhesana, Suman Chatterjee, Dermot Brabazon   +3 more
wiley   +1 more source

Neonatal jaundice and its association with sepsis, birth trauma, and prolonged labor in Ethiopia: A systematic review and meta-analysis

International Journal of Africa Nursing Sciences
Background: No comprehensive nationwide evidence exists regarding neonatal jaundice in Ethiopia. Hence, this study aimed to determine the pooled prevalence of neonatal jaundice and explore its relationship with sepsis, birth trauma, and prolonged labor ...
Bezawit Adane, Melaku Yalew, Elsabeth Addisu, Mastewal Arefaynie, Kefale Mitiku, Yitbarek Wasihun, Tilahun Degu Tsega, Mahider Awoke, Tezera Asfaw, Bereket Kefale, Yitayish Damtie, Natnael Kebede   +11 more
doaj   +1 more source

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12 ‐Related Developmental Disorders

American Journal of Medical Genetics Part A, Volume 200, Issue 7, Page 1619-1650, July 2026.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

Epidemiological study investigating the main biochemical profile related to Neonatal Jaundice in Department of Pediatric in Zaliten teaching hospital in Libya

مجلة جامعة الزيتونة, 2023
Jaundice due to indirect hyperbilirubinemia of the newborn is a common and frequent cause of neonatal admissions to healthcare facilities worldwide.
Ryad Alati, Abdulati Salem, Mahmud Abushhewa   +2 more
doaj  

PHLPP is neither a Phosphatase nor a Tumor Suppressor

BioEssays, Volume 48, Issue 7, July 2026.
PH domain leucine‐rich repeat protein phosphatases (PHLPP) have been described as Akt phosphatases and tumor suppressors for more than 20 years. Recent evidence, however, indicates that they are pseudophosphatases that lost catalytic activity more than 450 Mya. This article argues that new hypotheses are urgently needed to reorient the field.
Thomas A. Leonard
wiley   +1 more source

Genetically Confirmed Osteogenesis Imperfecta (COL1A1) With Unexplained Ambiguous Genitalia in a 46,XY Child: An Index Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
A 6‐year‐old child with a rare dual diagnosis confirmed by genetic testing ‐ osteogenesis imperfecta (blue sclerae, disproportionate short stature) and concurrent 46,XY disorder of sex development (micropenis, hypospadias, impalpable gonads). ABSTRACT Osteogenesis imperfecta (OI) is a heritable disorder of type I collagen characterized by bone ...
Harshita Agarwal, Tathagata Jha, Mohammad Orooj Azmi, Soumita Sarkar, Vinay Suresh   +4 more
wiley   +1 more source

Neonatal graves’ disease complicated with cholestatic jaundice: a case report [PDF]

Background Neonatal cholestatic jaundice and elevated liver enzymes can result from various etiologies, including anatomical, infectious, endocrine, and metabolic abnormalities.
Bei Luo, Hong Jing, Hui Wang, Ya-Ping Tian, Xue-Feng Zhang   +4 more
core   +1 more source

Twin‐To‐Twin Transfusion Syndrome in Dichorionic‐Triamniotic Triplets Successfully Managed Without Fetoscopic Laser: A Management‐Focused Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Triplet pregnancies are rare (~0.1% of births) and often complicated by prematurity. When one placental unit is monochorionic, there is a risk of twin‐to‐twin transfusion syndrome (TTTS), a severe vascular imbalance affecting monochorionic gestations.
Ammir Abuzahra, Safwat Jabari, Mohammad Rabaee, Saja Atawneh, Shaimaa Sweity, Rasmiya Qawasmi, Omar Hammam Salloum   +6 more
wiley   +1 more source

Predicting severe neonatal jaundice from maternal risk factors [PDF]

, 2019
This is an invited speaker lecture on Predicting Severe Neonatal Jaundice from Maternal Risk Factors. Outline of Lecture : 1. Definition of Severe Neonatal Jaundice 2. Maternal Risk Factors 3.
Ismail, Hamizah
core