Event Videos

https://pubmed.ncbi.nlm.nih.gov/36332083/ Autoimmune liver disease

J Pediatr Gastroenterol Nutr. 2022 Nov 3.
doi: 10.1097/MPG.0000000000003654.Online ahead of print.

Hepatic dry copper weight in paediatric autoimmune liver disease

Jeremy S Nayagam 1 2, Deepak Joshi 1, Richard J Thompson 1 2, Anil Dhawan 3, Nedim Hadzic 3, Claudia Mestre-Alagarda 1, Maesha Deheragoda 1, Marianne Samyn 1
Affiliations expand
PMID: 36332083

DOI: 10.1097/MPG.0000000000003654
Full text linksCite
Abstract
Objectives: Elevated hepatic dry copper weight is recognised in adults with autoimmune liver disease (AILD) and chronic cholestasis. We aim to review hepatic dry copper weight in paediatric AILD.

Published on: 
Nov-2022

https://pubmed.ncbi.nlm.nih.gov/36397404/ liver transplant

Medicine (Baltimore). 2022 Nov 11;101(45):e31156.
doi: 10.1097/MD.0000000000031156.

Bone demineralization in a cohort of Egyptian pediatric liver transplant recipients: Single center pilot study

Magd A Kotb 1, Lubna A Fawaz 1, Rania A Zeitoun 2, Yomna M Shaalan 1, Nazira Aly 1, Hesham Abd El Kader 3, Gamal El Tagy 4, Haytham Esmat 4, Alaa F Hamza 3, Hend Abd El Baky 1

Abstract

Published on: 
Nov-2022

https://pubmed.ncbi.nlm.nih.gov/36447259/ liver transplant

Child Adolesc Psychiatry Ment Health. 2022 Nov 29;16(1):94.
doi: 10.1186/s13034-022-00516-4.

Mental health in children with living donor liver transplantation: a propensity score-matched analysis

Mingzhu Huang # 1, Yuchen Hou # 1 2, Wen Li # 3, Guanghai Wang 4 5 6, Guangxiang Gu 7 8, Qiang Xia 9

Abstract
Background: This study explored mental health of pediatric patients with living donor liver transplantation.

Published on: 
Nov-2022

https://pubmed.ncbi.nlm.nih.gov/36399011/ galactosemia

J Pediatr Endocrinol Metab. 2022 Nov 21.
doi: 10.1515/jpem-2022-0308. Online ahead of print.

All aspects of galactosemia: a single center experience

Abdurrahman Akgun 1, Yasar Dogan 2
Affiliations expand
PMID: 36399011

DOI: 10.1515/jpem-2022-0308
Full text linksCite
Abstract

Objectives: Classic galactosemia is a galactose metabolism disorder due to galactose-1-phosphate uridyltransferase deficiency. In this study we report the clinical features of a cohort of children with classic galactosemia.

Published on: 
Nov-2022

https://pubmed.ncbi.nlm.nih.gov/36451692/ liver failure

Pediatr Gastroenterol Hepatol Nutr. 2022 Nov;25(6):481-488.
doi: 10.5223/pghn.2022.25.6.481.Epub 2022 Nov 2.

Effectiveness of High-Volume Therapeutic Plasma Exchange for Acute and Acute-on-Chronic Liver Failure in Korean Pediatric Patients

Hyeji Lim 1 2, Yunkoo Kang 3, Sowon Park 1 2, Hong Koh 1 2

Abstract
Purpose: Liver transplantation (LT) is the only curative treatment for acute liver failure (ALF) and acute-on-chronic liver failure (ACLF). In high-volume therapeutic plasma exchange (HV-TPE), extracorporeal liver support filters accumulate toxins and improve the coagulation factor by replacing them. In this study, we aimed to evaluate the effectiveness of HV-TPE in pediatric patients with ALF and ACLF.

Published on: 
Nov-2022

https://pubmed.ncbi.nlm.nih.gov/36445055/ liver failure

Turk J Gastroenterol. 2022 Nov 29.
doi: 10.5152/tjg.2022.22062. Online ahead of print.

Extracorporeal Therapies in Children with Acute Liver Failure: A Single-Center Experience

Emrah Gün 1, Ayşen Durak 2, Edin Botan 1, Selen Şimşek Pervane 2, Anar Gurbanov 1, Burak Balaban 1, Fevzi Kahveci 1, Hasan Özen 1, Hacer Uçmak 1, Fulden Aycan 1, Zarife Kuloğlu 3, Tanıl Kendirli 1

Abstract
Background: The aim of this study is to determine the indication, timing, and administration of extracorporeal therapies such as total plasma exchange and continuous renal replacement therapy in children with acute liver failure or acute-on-chronic liver failure.

Published on: 
Nov-2022

https://pubmed.ncbi.nlm.nih.gov/36451695/ liver transplant

Pediatr Gastroenterol Hepatol Nutr. 2022 Nov;25(6):489-499.
doi: 10.5223/pghn.2022.25.6.489.Epub 2022 Nov 2.

Pediatric Liver Transplantation: Caregivers' Quality of Life

Ana Paula Bastos Tavares 1, Lucas Belém Pessôa de Melo Guerra Seixas 1, Caren Lopes Wanderlei Jayme 1, Gilda Porta 2, Renata Belém Pessôa de Melo Seixas 1, Elisa de Carvalho 1

Abstract

Published on: 
Nov-0022

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