Results 111 to 120 of about 116,093 (277)

The non-HDL-C to APOB ratio as a predictor of inaccurate LDL-C measurement in patients with chronic intrahepatic cholestasis and jaundice: a retrospective study [PDF]

PeerJ
Background Cholestasis is characterized by the accumulation of bile in the liver or biliary system due to obstruction or impaired flow, necessitating lipid profiling to assess lipid metabolism abnormalities.
Yongjiang Cheng, Jingyan Ye, Junyuan Huang, Yang Wang   +3 more
doaj   +2 more sources

Regionally acquired intestinal failure data suggest an underestimate in national service requirements [PDF]

, 2009
Objectives, setting and patients: With complete case referral for prolonged parenteral nutrition (PN) beyond term equivalent, serving a stable population of 1.25 million people, we describe the long-term outcome and survival of patients referred to an ...
Barclay, Andrew, GI/Nutrition Research Fund, Child Life and Health, University of Edinburgh (Funder), Gillett, Peter, Hoole, David, Livingstone, Jennifer, Menon, Gopi, Munro, Fraser, Paxton, Catherine E, Wilson, David C, Young, David   +9 more
core   +1 more source

A review of the methodological features of systematic reviews in maternal medicine [PDF]

, 2007
Background In maternal medicine, research evidence is scattered making it difficult to access information for clinical decision making. Systematic reviews of good methodological quality are essential to provide valid inferences and to produce usable ...
A Conde-Agudelo, A Coomarasamy, A Coomarasamy, AD Oxman, AD Oxman, AR Jadad, CL Dennis, CL Dennis, CT Beck, CT Beck, DA Scott, E Boath, G Kovalevsky, HL Kwon, HS Sacks, IA Greer, IP Kosmas, IP Kosmas, JC Gluck, JH Goodman, JL Kujovich, K Duckitt, Khalid S Khan, LA Magee, LA Magee, Lumaan Sheikh, M Clarke, M Eberhard-Gran, M Egger, M Lassere, M Petticrew, Mark D Kilby, MP Austin, MP Austin, MP Austin, SC Brody, Shakila Thangaratinam, Shelley Johnston, T Brien, VE Murphy, WF Rayburn   +40 more
core   +6 more sources

Facial features in Alagille syndrome: Specific or cholestasis facies? [PDF]

, 2002
Binita M. Kamath, Kathleen M. Loomes, Rebecca J. Oakey, Karan E.M. Emerick, Tracy Conversano, Nancy B. Spinner, David A. Piccoli, Ian D. Krantz   +7 more
openalex   +1 more source

Depletion and enrichment of phytosterols in soybean oil lipid emulsions directly associate with serum markers of cholestasis in preterm parenteral nutrition–fed pigs

, 2021
Gregory Guthrie, Barbara J. Stoll, Shaji Chacko, Mahmoud A. Mohammad, Candace C. Style, Mariatu A. Verla, Oluyinka O. Olutoye, Deborah Schady, Charlotte Lauridsen, Nicholas M Tataryn, Douglas G. Burrin   +10 more
openalex   +2 more sources

P0203 ERYTHROCYTE POLYAMINE CONCENTRATION IS RELATED TO THE COURSE OF CHRONIC CHOLESTASIS [PDF]

, 2004
Piotr Socha, Adam Fogel, K. Sasiak, Irena Jankowska, Michael S. Adamowicz, Joanna Pawłowska, J Socha   +6 more
openalex   +1 more source

Recessive Mutations in KIF12 Cause High Gamma‐Glutamyltransferase Cholestasis

Hepatology Communications, 2019
Undiagnosed liver disease remains an unmet medical need in pediatric hepatology, including children with high gamma‐glutamyltransferase (GGT) cholestasis. Here, we report whole‐exome sequencing of germline DNA from 2 unrelated children, both offspring of
Aysel Ünlüsoy Aksu, Subhash K. Das, C. Nelson-Williams, D. Jain, Ferda Özbay Hoşnut, Gülseren Evirgen Şahin, R. Lifton, S. Vilarinho   +7 more
semanticscholar   +1 more source

Intrahepatic Cholestasis [PDF]

BMJ, 1964
D F, ROBERTS, R E, TANNER
openaire   +2 more sources

Macrophage-derived IL-1β/NF-κB signaling mediates parenteral nutrition-associated cholestasis

Nature Communications, 2018
In infants intolerant of enteral feeding because of intestinal disease, parenteral nutrition may be associated with cholestasis, which can progress to end-stage liver disease.
K. E. El Kasmi, Padade M. Vue, Aimee L. Anderson, M. Devereaux, Swati Ghosh, N. Balasubramaniyan, S. Fillon, Carola Dahrenmoeller, A. Allawzi, Crystal Woods, S. McKenna, C. Wright, Linda K. Johnson, A. D’Alessandro, J. Reisz, E. Nozik-Grayck, F. Suchy, R. Sokol   +17 more
semanticscholar   +1 more source

SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN)

Genetics in Medicine, 2018
Biallelic mutations in SCYL1 were recently identified as causing a syndromal disorder characterized by peripheral neuropathy, cerebellar atrophy, ataxia, and recurrent episodes of liver failure.
Dominic Lenz, P. Mcclean, A. Kansu, P. Bonnen, G. Ranucci, C. Thiel, B. Straub, I. Harting, B. Alhaddad, Bianca Dimitrov, U. Kotzaeridou, Daniel Wenning, R. Iorio, R. Himes, Z. Kuloğlu, E. Blakely, Robert W. Taylor, T. Meitinger, S. Kölker, H. Prokisch, G. Hoffmann, T. Haack, C. Staufner   +22 more
semanticscholar   +1 more source