Results 191 to 200 of about 58,406 (311)

Clinical Features of Urinary Tract Infection in Neonates with Hyperbilirubinemia: A Cross-sectional Study

, 2023
Syed Mustafa Hasan, Gaurav Jain, Jyoti Meena, Sameer Punia   +3 more
openalex   +1 more source

DPMAS in the Management of Severe Acute Liver Injury

Case Reports in Hepatology, Volume 2026, Issue 1, 2026.
Background Acute liver injury is a severe disease in which a hepatic and later systemic inflammatory response is triggered, generally induced by paracetamol intoxication, undetermined causes, drugs, and hepatotropic and nonhepatotropic viruses. Case Summary A 67‐year‐old immunocompetent male with severe acute liver injury secondary to Cytomegalovirus ...
Maiko Alejandro Tavera Díaz, Annia Aguilar Loayza, Carolina Beatriz Mejía Vargas, Juan Fernando Mamani Ochoa, Sreeja Dattachoudhury   +4 more
wiley   +1 more source

Effect of Delayed Cord Clamping on Respiratory Infection-Related Encounters in the First 6 Months of Life in an Urban Community Hospital. [PDF]

Int J Pediatr
Gordon R, Neupane N, Pedraza Gonzalez L, Bloomfield L, McGrath-Blagrove T, Robitsek RJ, Pinero-Bernardo S, Cohen L, Lew LQ.   +8 more
europepmc   +1 more source

Hyperbilirubinemia in a Patient Receiving Alectinib for Anaplastic Lymphoma Kinase Positive Non-Small-Cell Lung Cancer: A Histological Features

Qian Zhang, Lei Yan, Yu-Jie Bao, Xiaoling Yuan, Donglin Yin, Jie Xu   +5 more
openalex   +2 more sources

Case Series: Hyperbilirubinemia under elexacaftor/tezacaftor/ivacaftor in the presence of Gilbert’s syndrome [PDF]

Julia Weitzel, Matthias Welsner, Christian Taube, Manfred Ballmann, Sivagurunathan Sutharsan   +4 more
openalex   +1 more source

Impact of Light Emitting Diode Phototherapy in Full-Term Neonates with Hyperbilirubinemia

, 2023
B. Suba Rajinikanth, R. Gokul Krishnan, Pramita Gayatri   +2 more
openalex   +1 more source

Syndromic Congenital Heart Disease Diagnosed in Adulthood: A Reminder of the Phenotypic Variability of Alagille Syndrome

Case Reports in Cardiology, Volume 2026, Issue 1, 2026.
Alagille syndrome is a rare multisystemic genetic condition most commonly associated with neonatal liver disease. Variable expressivity is a defining feature of Alagille syndrome, resulting in a broad spectrum of phenotypic variation among individuals who meet the diagnostic criteria. We present an atypical case of cardiac‐predominant Alagille syndrome
Matthew K. Campbell, Jessica Hallam, Samuel L. Casella, Sangeeta Shah, Kathleen Ngu   +4 more
wiley   +1 more source

StAR Protein Deficiency in Clinical Practice: A Case Series From Saudi Arabia

Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.
Objectives Steroidogenic acute regulatory (StAR) protein deficiency is a rare autosomal recessive disorder that disrupts steroid hormone biosynthesis, resulting in congenital adrenal hyperplasia (CAH) and variations in sexual development. However, limited data is available in Saudi Arabia.
Abeer Alabduljabbar, Dania Farooq, Sara Abid, Sara Aljazaeri, Raghad Alhuthil, Afaf Alsagheir, Kalyani Sen   +6 more
wiley   +1 more source

Retraction: Correlations between parameters of glycaemic variability and foetal growth, neonatal hypoglycaemia and hyperbilirubinemia in women with gestational diabetes. [PDF]

PLoS One
PLOS One Editors.
europepmc   +1 more source

Hyperbilirubinemia results in reduced oxidative injury in neonatal gunn rats exposed to hyperoxia

, 1995
Phyllis A. Dennery, Antony F. McDonagh, Douglas R. Spitz, Pamela A. Rodgers, David K. Stevenson   +4 more
openalex   +1 more source