Event Videos

https://pubmed.ncbi.nlm.nih.gov/36574286/ Acute liver failure

Eur J Gastroenterol Hepatol. 2022 Dec 23.
doi: 10.1097/MEG.0000000000002499.Online ahead of print.

Pediatric acute liver failure in Saudi Arabia: prognostic indicators, outcomes and the role of genetic testing

Abdulhamid Alhadab 1, Hadeel AlShihabi 2, Fatema Mohamed 2, Zahra AlDuhilib 2, Zahid Arain 3, Razan Bader 3

Abstract
Objective: The objective of this study was to determine the etiologies, outcomes, prognostic indicators and the role of genetic testing in children with acute liver failure (ALF).

Published on: 
Dec-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/36580335/ drug induced hepatitis

JAMA Netw Open. 2022 Dec 1;5(12):e2248803.
doi: 10.1001/jamanetworkopen.2022.48803.

Association of Inherited Genetic Factors With Drug-Induced Hepatic Damage Among Children With Acute Lymphoblastic Leukemia

Wenjian Yang 1, Seth E Karol 2, Keito Hoshitsuki 1, Shawn Lee 1, Eric C Larsen 3, Naomi Winick 4, William L Carroll 5, Mignon L Loh 6, Elizabeth A Raetz 5, Stephen P Hunger 7, Stuart S Winter 8, Kimberly P Dunsmore 9, Meenakshi Devidas 10, Mary V Relling 1, Jun J Yang 1 2

Abstract

Published on: 
Dec-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/36581321/ Transplant
Clin Transplant. 2022 Dec 29;e14894.
 doi: 10.1111/ctr.14894. Online ahead of print.
Incidence and risk factors of subclinical rejection after pediatric liver transplantation, and impact on allograft fibrosis
Zhixin Zhang 1,  Shengqiao Zhao  1,  Zhuyuan Si  1,  Zhenglu Wang  2, Chong Dong 2, Chao Sun 2,  Weiping Zheng  2, Wang Kai 2, Wei Zhang 2,  Zhuolun Song  2, Wei
Gao 2, Zhongyang Shen 2
Abstract
Intro: Subclinical rejection (SCR) is a common injury in protocol biopsy after pediatric liver transplantation (pLT), but its effect on the recipient is not clearly understood. We herein investigated the incidence and risk factors involved in SCR and analyzed the relationship between SCR and allograft fibrosis (AF).

Published on: 
Dec-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/36070526/ hepatitis

J Pediatr Gastroenterol Nutr. 2022 Nov 1;75(5):553-555.
doi: 10.1097/MPG.0000000000003603. Epub 2022 Sep 6.
Hepatitis-associated Aplastic Anemia
Maxime Gonnot 1, Florent Neumann 2, Frédéric Huet 1, Raphaëlle Maudinas 1, Thierry Leblanc 3, Florence Lacaille 4
Affiliations expand
PMID: 36070526

DOI: 10.1097/MPG.0000000000003603
Full text linksCite
Abstract

Published on: 
Nov-2022

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

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