Results 81 to 90 of about 165,982,891 (200)

An Approach to Antibody‐Mediated Rejection in Pediatric Liver Transplantation

open access: yesPediatric Transplantation, Volume 30, Issue 9, September 2026.
ABSTRACT Antibody‐mediated rejection (AMR) is an important but infrequent cause of pediatric liver allograft injury. There is a lack of standardized guidance, and treatment approaches vary across institutions. A writing group from the Society of Pediatric Liver Transplantation conducted a comprehensive review of the published literature and collected ...
Catalina Jaramillo   +8 more
wiley   +1 more source

Intrahepatic cholestasis of pregnancy. Diagnosis. Maternal and fetal complications [PDF]

open access: yes, 2020
Department of Obstetrics and Gynecology, Nicolae Testemitanu State University of Medicine and Pharmacy, Chisinau, Republic of Moldova, The 8th International Medical Congress for Students and Young Doctors, September 24-26, 2020Introduction ...
Butucel, Ana
core   +1 more source

A novel case report of benign recurrent intrahepatic cholestasis-associated USP53 genetic mutation in a Pakistani girl

open access: yesSAGE Open Medical Case Reports
Benign recurrent intrahepatic cholestasis is an autosomal recessive disorder presenting with intermittent episodes of cholestatic jaundice. The initial episode of benign recurrent intrahepatic cholestasis tends to occur within the first two decades of a ...
Tafiya Erum Kamran   +7 more
doaj   +1 more source

Intrahepatic cholestasis of pregnancy in Chile: Analysis of epidemiological change and a microbiological hypothesis

open access: yesMedwave
Intrahepatic cholestasis of pregnancy is a gestational pathology with an unusual epidemiological and pathophysiological behavior that remains partially unexplained. Its current global incidence ranges from 0.1% to 2%.
Cristian Contreras Vidal   +1 more
doaj   +1 more source

Association of ABCB4 and ABCB11 nucleotide variants with intrahepatic cholestasis of pregnancy

open access: yesJournal of Medical Science, 2019
Background. Intrahepatic cholestasis of pregnancy (ICP) is the most common liver disorder during gestation. The exact pathogenesis of ICP is multifactorial and still unclear.
Milena Gruszczyńska-Losy   +5 more
doaj   +1 more source

The pharmacological management of intrahepatic cholestasis of pregnancy.

open access: yes, 2011
Intrahepatic cholestasis of pregnancy is the most common liver disease occurring in the second half of pregnancy, characterized by pruritus and elevated serum bile acids often coupled to abnormal liver tests.
Lisotti A   +4 more
core   +1 more source

Diagnosis and course of pregnancy and childbirth in women with intrahepatic cholestasis of pregnancy: Summary of Ph.D. Thesis in Medical Sciences: 321.15. Obstetrics and Gynecology

open access: yes, 2023
Thesis structure. The thesis is laid out on 124 pages of main text, consisting of an introduction, 5 chapters, general conclusions, recommendations, and a bibliographic index of 255 references, 25 figures, 11 tables, and 10 annexes.
Cemortan, Maria
core   +1 more source

The dermatoses of pregnancy

open access: yesIndian Journal of Dermatology, 2008
The skin changes in pregnancy can be either physiological (hormonal), changes in pre-existing skin diseases or development of new pregnancy specific dermatoses.
Sachdeva Silonie
doaj  

Genetic Cholestasis: Lessons from the Molecular Physiology of Bile Formation

open access: yesCanadian Journal of Gastroenterology, 2000
Progressive familial intrahepatic cholestasis (PFIC) is a group of severe genetic cholestatic liver diseases of early life. PFIC types 1 and 2 are characterized by cholestasis and a low to normal serum gamma-glutamyltransferase (GGT) activity, whereas in
Peter LM Jansen, Michael Müller
doaj   +1 more source

Transcriptional regulation of hepatobiliary transport systems in health and disease: Implications for a rationale approach to the treatment of intrahepatic cholestasis

open access: yesAnnals of Hepatology, 2005
Hepatobiliary transport systems mediate hepatic uptake and biliary excretion of bile acids, bilirubin and other biliary constituents. Hereditary or acquired defects of these transporters may cause or maintain cholestasis and jaundice under various ...
Martin Wagner, Michael Trauner
doaj   +1 more source

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