Results 91 to 100 of about 5,947 (218)
European Journal of Haematology, Volume 117, Issue 1, Page 24-41, July 2026.ABSTRACT Acute lymphoblastic leukaemia (ALL) in older adults represents a growing clinical challenge, driven by an ageing population, adverse disease biology, and reduced tolerance to intensive chemotherapy. Although pediatric‐inspired regimens have improved outcomes in younger adults with Philadelphia chromosome (Ph)‐negative ALL, survival in older ...
Antonella Bruzzese +12 more
wiley +1 more source
RISK FACTORS OF RETINOPATHY OF PREMATURITY IN CHILDREN BORN FROM MULTIPLE PREGNANCIES
Офтальмохирургия, 2017 Purpose. To identify significant risk factors for the «threshold» retinopathy of prematurity (ROP) in children born from multiple pregnancies.Material and methods. The paper is based on a retrospective analysis of case histories of premature infants with
I. E. Panova +2 more
doaj +1 more source
Liver International, Volume 46, Issue 7, July 2026.ABSTRACT Background and Aims Herpes simplex virus (HSV) infection is common worldwide, but hepatic involvement is rare. HSV hepatitis is an uncommon yet frequently catastrophic cause of acute hepatitis and acute liver failure (ALF), accounting for < 1% of ALF cases while carrying very high mortality when diagnosis and antiviral therapy are delayed ...
Mario U. Mondelli +5 more
wiley +1 more source
Biochemical and molecular aspects of genetic disorders of bilirubin metabolism
, 1998 Bilirubin, the oxidative product of heme in mammals, is excreted into the bile after its esterification with glucuronic acid to polar mono- and diconjugated derivatives.
Yoshikazu Emi +5 more
core +1 more source
Extranodal natural killer/T‐cell lymphoma: From fatal to curable
CA: A Cancer Journal for Clinicians, Volume 76, Issue 4, July/August 2026.Abstract Extranodal natural killer (NK)/T‐cell lymphoma (ENKTCL) is one of the most aggressive non‐Hodgkin lymphomas characterized by NK‐cell or T‐cell origins, a geographic prevalence in Asian and South American populations, and Epstein–Barr virus (EBV) infection.
Jie Xiong +12 more
wiley +1 more source
Inherited Disorders of Bilirubin Metabolism [PDF]
, 2013 Inherited disorders of bilirubin metabolism - hereditary hyperbilirubinemias - are metabolic disorders manifested in early childhood. Unconjugated hyperbilirubinemias result from the defect of the enzyme uridine diphosphoglucuronosyltransferase (UGT1A1).
Šlachtová, Lenka
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Pathologic Features of Hereditary Cholestatic Diseases
, 2018 The inherited diseases causing conjugated hyperbilirubinemia are diverse, with variability in clinical severity, histologic appearance, and time of onset.
Andrew D. Clouston, Clouston, Andrew D.
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Significance of UGT1A1*28 genotype in patients with advanced liver injury caused by chronic hepatitis C [PDF]
Journal of Medical Biochemistry, 2019 Background: Chronic hepatitis C (CHC) is a significant cause of liver related morbidity and mortality worldwide. The role of genetics in the host response to hepatitis C virus is not elucidated. Genetic variations in UGT1A1 gene are the most common cause
Jordović Jelena +13 more
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Egyptian Pediatric Association GazetteBackground Neonatal cholestasis is a multifactorial disorder that may result from metabolic, infectious, or genetic etiologies. Dehydrated hereditary stomatocytosis (DHS), a rare autosomal dominant hemolytic anemia caused by PIEZO1 gene mutations, is ...
Deepak Borde +3 more
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Infantile Pyknocytosis in a Premature Dichorionic Diamniotic Twin
, 2021 Infantile pyknocytosis is a rare and self-limiting cause of hemolytic anemia in neonates. It can result in severe anemia and hyperbilirubinemia. The pathogenesis is unknown: a genetic origin has been discussed; however, based on the current literature it
van Wijk, Richard +3 more
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