Results 51 to 60 of about 24,959 (186)
Bardet–Biedl syndrome with choledochal cyst: Rare association with a novel variant
Journal of Indian Association of Pediatric Surgeons, 2023 Bardet–Biedl syndrome is an autosomal-recessive ciliopathic disorder affecting multiple organ systems. Characteristic features include progressive retinal dystrophy, obesity, polydactyly hypogonadism, mental retardation, and renal disorders.
Saket Kumar +4 more
doaj +1 more source
iRADIOLOGY, EarlyView.Selecting appropriate driver material and vibration frequency is essential for reliable myocardial stiffness measurement using magnetic resonance elastography. Optimized settings can enhance accuracy for cardiac stiffness assessment. ABSTRACT Background Myocardial stiffness is a crucial indicator of cardiac function and is associated with various ...
Yong Cheng +12 more
wiley +1 more source
Journal of Parenteral and Enteral Nutrition, EarlyView.Abstract Background Parenteral nutrition–associated liver disease is a severe complication in very low birth weight (≤1500 g) preterm neonates. Although previous pairwise meta‐analyses have compared individual intravenous lipid emulsions, their relative efficacy across all available formulations has not been established in this population.
Maria Di Chiara +2 more
wiley +1 more source
JPGN Reports, EarlyView.Abstract Hereditary fructose intolerance (HFI) typically presents in infancy with acute metabolic crisis upon the introduction of fructose. We report a case of a 13‐year‐old female with chronic abdominal pain, short stature, and persistent mild transaminitis.
Alexandra Hurlock +4 more
wiley +1 more source
Congenital Hepatic Fibrosis and Need for Liver Transplantation
International Journal of Organ Transplantation Medicine, 2010 Herein, we describe two patients who underwent liver transplantation with the clinical diagnosis of hepatic failure and cryptogenic cirrhosis; histopathology of the explanted hepatectomy specimen revealed congenitalhepatic fibrosis.
B. Geramizadeh +6 more
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Congenital biliary atresia in a Beefmaster calf
Brazilian Journal of Veterinary Pathology, 2016 Biliary atresia is a congenital cholangiopathy characterized by a progressive fibrosis of the bile ducts leading to impaired biliary flow, hepatic failure, icterus and early death.
Johnatan A. Ruíz-Ramírez +6 more
doaj +1 more source
Congenital hepatic fibrosis [PDF]
Postgraduate Medical Journal, 1967 A R, Lorimer, J, McGee, S G, McAlpine
openaire +4 more sources
JPGN Reports, EarlyView.ABSTRACT Esophageal varices (EV) need monitoring in patients with portal hypertension. In 2022, a single‐use ultra‐slim (3.5 mm) gastroscope was approved for use in children and adults. This study evaluated if an ultra‐slim gastroscope could evaluate, grade, and corroborate the presence of EV in sedated pediatric patients as compared to standard oral ...
Vishruti Patel +6 more
wiley +1 more source
Mass Spectrometry Reviews, EarlyView.ABSTRACT The use of MALDI mass spectrometry for the analysis of carbohydrates and glycoconjugates is a well‐established technique and this comprehensive review is the twelfth update of the original article published in 1999 and brings coverage of the literature to the end of 2024.
David J. Harvey
wiley +1 more source
A 40 years old woman with monolobar Caroli’s syndrome treated by left hepatic lobectomy
Journal of Research in Medical Sciences, 2007 Caroli’s disease (CD) is a rare congenital abnormality characterized by dilatation of intra hepatic bile ducts, which causes stone formation, recurrent cholangitis and higher risk for biliary malignancy.
Hamid Tavakkoli +5 more
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