Results 81 to 90 of about 1,143,701 (190)

Acute Neurological Events in Children With Hemoglobin SC Disease: A Multicenter Retrospective Study

Pediatric Blood &Cancer, Volume 73, Issue 11, November 2026.
ABSTRACT Introduction Neurological manifestations in children with hemoglobin SC (HbSC) disease remain insufficiently characterized, particularly regarding acute events. The aim of this study was to describe the spectrum and frequency of acute neurological events in a multicenter cohort of children with HbSC disease.
Célia Paulmin, Bérengère Koehl, Audrey Maudoux, Hanine Mansour, Marie‐Hélène Odievre, Nathalie Garrec, Emilie Georget, Cécile Arnaud, Slimane Allali, Lydia Doumdo, Marie Belloy, Corinne Guitton   +11 more
wiley   +1 more source

POTENTIALITY OF MODERN ULTRASOUND EVALUATION OF LIVER STRUCTURE BY THE EXAMPLE OF GILBERT’S SYNDROME

Педиатрическая фармакология, 2011
Technical advances in recent years have greatly expanded the diagnostic potentialities of ultrasound study, providing opportunities in a number of cases to diagnose and begin treatment as soon as possible.
M.I. Pykov, I.N. Zakharova, Z.V. Kaloeva
doaj   +2 more sources

Are novel and co‐xenic associations common in alien fungal and fungus‐like plant pathogens?

New Phytologist, Volume 252, Issue 2, Page 843-860, October 2026.
Possible scenarios for plant–pathogen associations during invasion. An introduced plant may occur in a new area without its pathogen (enemy release) or together with its pathogen (co‐introduction). The presence of the alien plant (in red) and its co‐introduced pathogen (in dark red) can result in pathogen spillover to co‐occurring plants. Host jumps to
Anna Schertler, Bernd Lenzner, Stefan Dullinger, Dietmar Moser, Adrián García‐Rodríguez, Irmgard Krisai‐Greilhuber, Hermann Voglmayr, Jennifer L. Bufford, Alberto Santini, Luisa Ghelardini, César Capinha, Luís Reino, Michael J. Wingfield, Marco Thines, Pedro Talhinhas, Wayne Dawson, Mark van Kleunen, Holger Kreft, Jan Pergl, Petr Pyšek, Patrick Weigelt, Marten Winter, Franz Essl   +22 more
wiley   +1 more source

Gilbert’s syndrome and antiviral therapy of hepatitis C

Annals of Hepatology, 2009
Treatment of chronic hepatitis C with type I interferons and ribavirin can be associated with exacerbation of hepatitis and sometimes liver decompensation.
Katja Deterding, Kurt Grüngreiff, Tim O. Lankisch, Andrej Potthoff, Matthias J. Bahr, Michael P. Manns, Heiner Wedemeyer, Christian P. Strassburg   +7 more
doaj   +1 more source

Hepatotoxicity caused by mebendazole in a patient with Gilbert's syndrome

, 2019
What is known and objective: Mebendazole (MBZ) is a broad‐spectrum antihelminthic agent of the benzimidazole type. Although MBZ has been reported to cause hepatic injury, case reports of severe hepatic injury are very rare.
Claudia Colomba, Antonio Cascio, Manlio Tolomeo, Maria Meli   +3 more
core   +1 more source

Pathological jaundice in full-term newborns and Gilbert’s syndrome

Zdravniški Vestnik, 2011
Background: In the course of our research on polymorphism in the UGT1A1 gene of healthy full-term newborns, we studied the relationship between pathological jaundice and the newborn’s genotype.
Danijela Furlan, Ana Ilijaš Trofenik, Barbara Ostanek, Zlata Felc, Borut Bratanič, Jana Lukač Bajalo   +5 more
doaj  

Pharmacokinetics of Josamycin in patients with liver cirrhosis and Gilbert's syndrome after repeated doses.

, 1985
The pharmacokinetics of Josamycin was studied in 31 subjects (10 normals, 9 Gilbert's syndrome and 12 compensated liver cirrhosis) after the administration of Josamycin (1 g orally) and in 13 subjects (4 normals, 4 Gilbert's syndrome and 5 compensated ...
ORLANDO, ROCCO, Miglioli PA, MURACA, MAURIZIO, Strazzabosco M, Berti T., R. Iemmolo, Okolicsanyi L, Biral A, Padrini G, G. Nassuato, Venuti M   +10 more
core  

Gilbert's syndrome in a newborn (a clinical case)

, 2021
Мета — показати особливості перебігу та лікування синдрому Жильбера в новонародженої дитини. Матеріали та методи. Наведено клінічний випадок власного спостереження за новонародженою дитиною з синдромом Жильбера.
Лебедева, Татьяна Николаевна, Цвіренко, Світлана Миколаївна, Щербань, Олена Анатоліївна, Лебедєва, Тетяна Миколаївна, Фесенко, Мария Евгеньевна, Liebiedieva, T. M., Fesenko, M. Yе., Козакевич, Вероніка Клавдіївна, Scherban, O. A., Kozakevych, V. K., Фесенко, Марія Євгенівна, Козакевич, Вероника Клавдиевна, Цвиренко, Светлана Николаевна, Щербань, Елена Анатолиевна, Tsvirenko, S. M.   +14 more
core  

Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes

Haematologica, 1999
BACKGROUND AND OBJECTIVE: Crigler-Najjar syndromes type I and II and Gilbert's syndrome are familial unconjugated hyperbilirubinemias caused by genetic lesions involving a single complex locus encoding for bilirubin-UDP-glucuronosyltransferase which is ...
M Sampietro, A Iolascon
doaj  

Refractory obstructive jaundice in a child affected with thalassodrepanocytosis: a new endoscopic approach

BMC Gastroenterology, 2010
Background Liver involvement, including elevated direct-reacting bilirubin levels, is common in patients with sickle cell disease. Fifty to seventy percent of sickle cell patients have pigmented gallstones due to precipitation of unconjugated bilirubin ...
Barresi Luca, Tarantino Ilaria, Di Pisa Marta, Sciveres Marco, Curcio Gabriele, Riva Silvia, Traina Mario   +6 more
doaj   +1 more source