Results 101 to 110 of about 139,121 (234)

Cellular mechanisms of intrahepatic cholestasis.

, 1990
Most forms of intrahepatic cholestasis are caused by a failure of hepatocytes to secrete osmotically active bile constituents into the minute channels of bile canaliculi.
Meier-Abt PJ
core   +1 more source

Benign recurrent intrahepatic cholestasis: late initial diagnosis in adulthood

Annals of Hepatology, 2010
Benign recurrent intrahepatic cholestasis (BRIC) is a rare autosomal recessive or sporadic disorder, characterized by recurrent episodes of intense pruritus and jaundice that resolve spontaneously without leaving considerable liver damage.
Fatih Ermis, MD, Kemal Oncu, Melih Ozel, Yusuf Yazgan, Ahmet Kemal Gurbuz, Levent Demirturk, Hakan Demirci, Taner Akyol, Aptullah Hahoglu   +8 more
doaj   +1 more source

Elevated red blood cell distribution width is associated with intrahepatic cholestasis of pregnancy [PDF]

, 2017
Objectives: Intrahepatic cholestasis of pregnancy is the most common pregnancy specific liver disease and related with adverse maternal and perinatal outcome.
Vural Yilmaz, Zehra; Zekai Tahir Burak Women’s Health Care, Training and Research Hospital, Ankara, Turkey, Yılmaz, Elif; Dr Sami Ulus Women’s Health and Diseases Training and Research Hospital, Uygur, Dilek; Zekai Tahir Burak Women's Health Care, Training and Research Hospital, Ankara, Turkey, Gencosmanoglu Turkmen, Gulenay; Zekai Tahir Burak Women's Health Care, Training and Research Hospital, Ankara, Turkey, Daglar, Korkut; Zekai Tahir Burak Women's Health Care, Training and Research Hospital, Ankara, Turkey, Kara, Ozgur; Zekai Tahir Burak Women's Health Care, Training and Research Hospital, Ankara, Turkey   +5 more
core   +1 more source

Clinical aspects of pregnancy and childbirth in women with intrahepatic cholestasis of pregnancy

One Health & Risk Management
Introduction. Intrahepatic cholestasis of pregnancy (ICP) is a liver pathology that has negative impact on progression of pregnancy and childbirth in affected women.
Maria CEMORTAN, Irina SAGAIDAC, Corina ILIADI-TULBURE, Olga CERNETCHI   +3 more
doaj   +1 more source

Intrahepatic Cholestasis of Pregnancy Leading to Severe Vitamin K Deficiency and Coagulopathy

Case Reports in Obstetrics and Gynecology, 2017
Intrahepatic cholestasis of pregnancy is seldom associated with significant vitamin K deficiency. We report a case of a 16-year-old primigravid patient at 24 weeks and 3 days of gestation who presented with pruritus, hematuria, and preterm labor ...
Maria Maldonado, Ali Alhousseini, Michael Awadalla, Jay Idler, Robert Welch, Karoline Puder, Manasi Patwardhan, Bernard Gonik   +7 more
doaj   +1 more source

Systematic review of progressive familial intrahepatic cholestasis.

Clinics And Research in Hepatology and Gastroenterology, 2019
BACKGROUND AND AIMS Progressive familial intrahepatic cholestasis (PFIC) is a heterogeneous group of rare genetic disorders associated with bile acid secretion or transport defects. This is the first systematic review of the epidemiology, natural history
A. Baker, N. Kerkar, L. Todorova, B. Kamath, R. Houwen   +4 more
semanticscholar   +1 more source

Progressive familial intrahepatic cholestasis with normal GGT level appearing with lichenification and enlargement of hands and feet

The Turkish Journal of Pediatrics, 2005
Progressive familial intrahepatic cholestasis is a serious disease of the liver, known as Byler disease, characterized by hepatocellular cholestasis.
Tümay Doğanci, Gülen Akyol, Sevcan Bulaç   +2 more
doaj  

Genetics and Molecular Modeling of New Mutations of Familial Intrahepatic Cholestasis in a Single Italian Center.

PLoS ONE, 2015
Familial intrahepatic cholestases (FICs) are a heterogeneous group of autosomal recessive disorders of childhood that disrupt bile formation and present with cholestasis of hepatocellular origin.
Isabella Giovannoni, Francesco Callea, Emanuele Bellacchio, Giuliano Torre, Jean De Ville De Goyet, Paola Francalanci   +5 more
doaj   +1 more source

Progressive familial intrahepatic cholestasis and benign recurrent intrahepatic cholestasis : a review

, 2012
Progressive familial intrahepatic cholestasis (PFIC) and benign recurrent intrahepatic cholestasis (BRIC) are two rare autosomal recessive disorders, characterized by cholestasis.
STRUBBE, BEATRIJS, Van Vlierberghe, Hans, Geerts, Anja, Colle, Isabelle   +3 more
core  

Progressive familial intrahepatic cholestasis type 4: a case report

Journal of Medical Case Reports
Background Progressive familial intrahepatic cholestasis is an autosomal recessive genetic disorder that manifests primarily with jaundice and pruritus and can progresses from persistent cholestasis to cirrhosis and late childhood liver failure ...
Mohamed Abdelmalak Abokandil, Saber Waheeb, Wessam Zaghloul, Manal Abdelgawad, Mona Abdelhady, Mohamed Mansy, Mostafa Kotb   +6 more
doaj   +1 more source