Simon Horslen
Overview
Explore the profile of Simon Horslen including associated specialties, affiliations and a list of published articles.
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75
Citations
924
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Recent Articles
1.
Abusuliman M, Jafri S, Summers B, Beduschi T, Boike J, Farmer D, et al.
Transplant Proc
. 2025 Jan;
57(2):380-389.
PMID: 39890513
Background: Intestinal transplantation (IT) is a complex procedure that requires nuanced immunosuppressive strategies to optimize patient outcomes. Despite advancements, significant variability remains in immunosuppressive protocols across transplant centers due to...
2.
Taylor S, Harpavat S, Gromer K, Andreev V, Loomes K, Bezerra J, et al.
Pediatr Res
. 2025 Jan;
PMID: 39881181
Background: The immune heterogeneity of biliary atresia (BA) presents a challenge for development of prognostic biomarkers. This study aimed to identify early immune signatures associated with biliary drainage after Kasai...
3.
Luo Y, Fraser L, Jezykowski J, Gupta N, Miethke A, Taylor S, et al.
Hepatology
. 2024 Dec;
PMID: 39693274
Background And Aims: Biliary atresia (BA) entails an inflammatory sclerosing lesion of the biliary tree, with prominent fibrosis in infancy. Previous studies revealed that neutrophil-activating IL-8 and neutrophil extracellular traps...
4.
Ashokkumar C, Ningappa M, Raghu V, Mazariegos G, Higgs B, Morgan P, et al.
Transplant Direct
. 2024 Feb;
10(3):e1589.
PMID: 38414976
Background: Enhanced B-cell presentation of donor alloantigen relative to presentation of HLA-mismatched reference alloantigen is associated with acute cellular rejection (ACR), when expressed as a ratio called the antigen presenting...
5.
Van Hove J, Friederich M, Strode D, Van Hove R, Miller K, Sharma R, et al.
Hepatol Commun
. 2024 Jan;
8(1).
PMID: 38180987
Background: Mitochondrial hepatopathies (MHs) are primary mitochondrial genetic disorders that can present as childhood liver disease. No recognized biomarkers discriminate MH from other childhood liver diseases. The protein biomarkers growth...
6.
Teckman J, Rosenthal P, Ignacio R, Spino C, Bass L, Horslen S, et al.
Hepatol Commun
. 2023 Dec;
7(12).
PMID: 38055647
Background: Our objective was to better understand the natural history and disease modifiers of Alpha-1-antitrypsin deficiency (AATD), a common genetic liver disease causing hepatitis and cirrhosis in adults and children....
7.
Glessner J, Ningappa M, Ngo K, Zahid M, So J, Higgs B, et al.
J Hepatol
. 2023 Aug;
79(6):1385-1395.
PMID: 37572794
Background & Aims: Biliary atresia (BA) is poorly understood and leads to liver transplantation (LT), with the requirement for and associated risks of lifelong immunosuppression, in most children. We performed...
8.
Deniz S, Schinner R, Monroe E, Horslen S, Srinivasa R, Lv Y, et al.
Cardiovasc Intervent Radiol
. 2023 Aug;
46(9):1203-1213.
PMID: 37532945
Purpose: The purpose of the study was to investigate outcome after pediatric transjugular intrahepatic portosystemic shunt (TIPS) with respect to survival MATERIAL AND METHODS: After searching for studies on TIPS...
9.
Ceulemans L, Dubois A, Clarysse M, Canovai E, Venick R, Mazariegos G, et al.
Ann Surg
. 2023 Jul;
278(5):807-814.
PMID: 37497671
Objective: To describe the worldwide experience with living donation (LD) in intestinal transplantation (ITx) and compare short-term and long-term outcomes to a propensity-matched cohort of deceased donors. Background: ITx is...
10.
Feldman A, Adams M, Griesemer A, Horslen S, Kelly B, Mavis A, et al.
Transplantation
. 2023 May;
107(6):1223-1225.
PMID: 37220339
No abstract available.