[HTML][HTML] Carleman estimates for semi-discrete parabolic operators and application to the controllability of semi-linear semi-discrete parabolic equations

F Boyer, J Le Rousseau - Annales de l'Institut Henri Poincare (C) Non …, 2014 - Elsevier
In arbitrary dimension, in the discrete setting of finite-differences we prove a Carleman
estimate for a semi-discrete parabolic operator, in which the large parameter is connected to …

[HTML][HTML] Structural and functional hepatocyte polarity and liver disease

P Gissen, IM Arias - Journal of hepatology, 2015 - Elsevier
Hepatocytes form a crucially important cell layer that separates sinusoidal blood from the
canalicular bile. They have a uniquely organized polarity with a basal membrane facing liver …

Guideline for the evaluation of cholestatic jaundice in infants: joint recommendations of the North American Society for Pediatric Gastroenterology, Hepatology, and …

R Fawaz, U Baumann, U Ekong… - Journal of pediatric …, 2017 - journals.lww.com
Cholestatic jaundice in infancy affects approximately 1 in every 2500 term infants and is
infrequently recognized by primary providers in the setting of physiologic jaundice …

Progressive familial intrahepatic cholestasis

LN Bull, RJ Thompson - Clinics in liver disease, 2018 - liver.theclinics.com
Bile was recognized by the ancient Greeks as 1 of the 4 humors; its importance is still
recognized in twenty-first century medicine, although maybe only by hepatologists. Bile …

Jaundice revisited: recent advances in the diagnosis and treatment of inherited cholestatic liver diseases

HL Chen, SH Wu, SH Hsu, BY Liou, HL Chen… - Journal of biomedical …, 2018 - Springer
Background Jaundice is a common symptom of inherited or acquired liver diseases or a
manifestation of diseases involving red blood cell metabolism. Recent progress has …

Progressive familial intrahepatic cholestasis

A Srivastava - Journal of clinical and experimental hepatology, 2014 - Elsevier
Progressive familial intrahepatic cholestasis (PFIC) is a group of rare disorders which are
caused by defect in bile secretion and present with intrahepatic cholestasis, usually in …

Cholestasis: Exploring the triangular relationship of gut microbiota-bile acid-cholestasis and the potential probiotic strategies

L Yu, Y Liu, S Wang, Q Zhang, J Zhao, H Zhang… - Gut …, 2023 - Taylor & Francis
Cholestasis is a condition characterized by the abnormal production or excretion of bile, and
it can be induced by a variety of causes, the factors of which are extremely complex …

[HTML][HTML] Pediatric hepatocellular carcinoma

R Khanna, SK Verma - World journal of gastroenterology, 2018 - ncbi.nlm.nih.gov
Pediatric hepatocellular carcinoma (HCC) is the second common malignant liver tumor in
children after hepatoblastoma. It differs from the adult HCC in the etiological predisposition …

[PDF][PDF] MYO5B mutations cause cholestasis with normal serum gamma‐glutamyl transferase activity in children without microvillous inclusion disease

E Gonzales, SA Taylor, A Davit‐Spraul, A Thébaut… - …, 2017 - Wiley Online Library
Some patients with microvillus inclusion disease due to myosin 5B (MYO5B) mutations may
develop cholestasis characterized by a progressive familial intrahepatic cholestasis‐like …

Genotype correlates with the natural history of severe bile salt export pump deficiency

DBE van Wessel, RJ Thompson, E Gonzales… - Journal of …, 2020 - Elsevier
Background & Aims Mutations in ABCB11 can cause deficiency of the bile salt export pump
(BSEP), leading to cholestasis and end-stage liver disease. Owing to the rarity of the …