Results 101 to 110 of about 674,474 (173)

Benign Recurrent Intrahepatic Cholestasis [PDF]

, 2020
openaire   +3 more sources

A Case Report of Dublin-Johnson Syndrome

پزشکی بالینی ابن سینا, 2000
Hyperbilirubinemia is a common manifestation in internal medicine. It is divided to conjugated and unconjugated hyperbilirubinemia . Conjugated hyperbilirubinemia usually results from hepatocellular or cholestatic liver disease or from extrahepatic ...
Amir Hooshang Mohammad Alizadeh
doaj  

Genetic and phenotypic features familial intrahepatic cholestasis: case report

Familial intrahepatic cholestasis is a heterogeneous group of genetic disorders affecting the secretion and transport of bile acids. Progressive familial intrahepatic cholestasis (PFIC) may debut at different periods of childhood and in adults. Currently,
E. A. Kurmaeva, G. A. Kulakova, R. R. Shaydullina, S. Ya. Volgina, A. I. Mukhamadieva, N. A. Solovieva   +5 more
core   +1 more source

Intrahepatic Cholestasis of Pregnancy

, 2014
Intrahepatic cholestasis of pregnancy is the most common pregnancy-specific liver disease that typically presents in the third trimester. The clinical features are maternal pruritus in the absence of a rash and deranged liver function tests, including ...
Geenes, Victoria, Williamson, Catherine
core   +1 more source

Benign Recurrent Intrahepatic Cholestasis — Unravelleing the Paradox

Indian Pediatrics, 2021
R, Ganesh, N, Suresh, Malathi, Sathiyasekeran, L, Venkatakrishnan   +3 more
openaire   +2 more sources

Prenatal Diagnosis of Progressive Familial Intrahepatic Cholestasis Type 2

, 2011
Background and Aim: Progressive familial intrahepatic cholestasis type 2 (PFIC2) results from genetic defects of the hepatobiliary bile salt export pump (BSEP, ABCB11) at chromosome 2q24.
CHEN, SZU-TAH;CHEN, HUEY-LING;SU, YI-NING;LIU, YU-JUNG;NI, YEN-HSUAN;HSU, HONG-YUAN;CHU, CHIA-HSIANG;WANG, NAI-YU;CHANG, MEI-HWEI, 陳思達;陳慧玲;蘇怡寧;劉有容;倪衍玄;許宏遠;朱家祥;王乃雩;張美惠   +1 more
core   +1 more source

[Recurrent benign intrahepatic cholestasis and their progression to familiar progressive intrahepatic cholestasis].

Revista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru, 2008
Benign recurrent intrahepatic cholestasis (BRIC) is a rare form of intrahepatic cholestasis characterized by repeated self-limited episodes of severe pruritus and jaundice. Classically its natural evolution is benign, without progress to fibrosis or hepatic insufficiency; although, lastly were reported cases which progress to Progressive familial ...
Marco, Alburquerque Miranda, Gloria, Vargas Cárdenas, Zenaida, Lozano Miranda, Tania, Reyes Mugruza, Walter, Li Torres, Mario, Valdivia Roldán   +5 more
openaire   +1 more source

Extracorporal albumin dialysis (MARS) improves cholestasis and normalizes low apo A-I levels in a patient with benign recurrent intrahepatic cholestasis (BRIC)

, 2002
The familial cholestatic diseases Benign Recurrent Intrahepatic Cholestasis (BRIC) and Progessive Familial Intrahepatic Cholestasis type 1 (PFIC1) are characterized by intermittent or permanently elevated plasma bile salt levels, therapy-resistant ...
Kuipers, F; id_orcid, Bijleveld, CMA, Franssen, CFM, Stellaard, F, Sturm, E, de Knegt, RJ, Staels, B, Gouw, A, Kuipers, F, Franssen, CFM; id_orcid, Boverhof, R   +10 more
core   +1 more source

Recurrent Cholestatic Jaundice in a Young Indian Adult: A Clinical Diagnosis of Benign Recurrent Intrahepatic Cholestasis. [PDF]

Cureus
Panda SS, Panda S, Jujharsingh A, Patra V.   +3 more
europepmc   +1 more source

Early plasmapheresis in type 2 benign recurrent intrahepatic cholestasis: A case report and review of literature. [PDF]

World J Hepatol
Heyerick L, Dhondt A, Van Vlierberghe H, Verhelst X, Raevens S, Geerts A.   +5 more
europepmc   +1 more source