Marek Stefanowicz
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Explore the profile of Marek Stefanowicz including associated specialties, affiliations and a list of published articles.
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26
Citations
46
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Recent Articles
1.
Swieszkowska E, Broniszczak D, Kalicinski P, Szymczak M, Stefanowicz M, Grajkowska W, et al.
Cancers (Basel)
. 2024 Sep;
16(17).
PMID: 39272968
Rhabdomyosarcoma (RMS) of the biliary tract is a rare tumor in children, constituting 0.5-0.8% of all pediatric RMS. Still, it is the most common malignancy in this location in children....
2.
Maruszewski P, Vilchez Monge A, Stefanowicz M, Szymczak M, Broniszczak D, Kowalski A, et al.
J Pediatr Gastroenterol Nutr
. 2024 Jul;
79(3):636-643.
PMID: 39014874
Objective: To determine the impact of infant recipient body weight at primary liver transplantation (LT) on both recipient and graft survival rates in complete national data from Poland. Methods: We...
3.
Li W, van der Doef H, Wildhaber B, Marra P, Bravi M, Pinelli D, et al.
BMJ Open
. 2024 Jun;
14(6):e081933.
PMID: 38866577
Introduction: Hepatic artery complications (HACs), such as a thrombosis or stenosis, are serious causes of morbidity and mortality after paediatric liver transplantation (LT). This study will investigate the incidence, current...
4.
Stefanowicz M, Kalicinski P, Ismail H, Kowalski A, Broniszczak D, Szymczak M, et al.
Children (Basel)
. 2024 Feb;
11(2).
PMID: 38397305
The aim of this study was to assess the long-term results of liver transplantation (LT) in pediatric patients with unresectable hepatoblastoma (HB) or hepatocellular carcinoma (HCC) with special reference to...
5.
Szymanska S, Markiewicz-Kijewska M, Pyzlak M, Kalicinski P, Teisseyre J, Czubkowski P, et al.
Minerva Pediatr (Torino)
. 2023 Jun;
PMID: 37284810
Background: Liver transplantation is currently a treatment of choice in patients with end-stage liver disease. Acute cellular rejection (ACR), antibody-mediated rejection (AMR), and chronic rejection (ChR) are major causes of...
6.
Kowalski A, Kowalewski G, Kalicinski P, Pankowska-Wozniak K, Szymczak M, Ismail H, et al.
Children (Basel)
. 2023 Feb;
10(2).
PMID: 36832502
A choledochal cyst is a rare malformation primarily diagnosed in children. The only effective therapy remains surgical cyst resection followed by Roux-en-Y hepaticojejunostomy. Treating asymptomatic neonates remains a point of...
7.
Stefanowicz M, Kalicinski P, Kowalewski G, Kowalski A, Ciopinski M, Szymczak M, et al.
Children (Basel)
. 2023 Feb;
10(2).
PMID: 36832468
The aim of our study was to assess risk factors for hepatic artery thrombosis (HAT) and to evaluate the impact of HAT management on long-term outcomes after pediatric living donor...
8.
Jarmolinski T, Rosa M, Rybka B, Ryczan-Krawczyk R, Gajek K, Bogunia-Kubik K, et al.
Front Pediatr
. 2022 Apr;
10:861692.
PMID: 35402365
We report a child with Fanconi anemia who, after hematopoietic stem cell transplantation (HSCT) complicated by acute graft-versus-host disease (GVHD), underwent orthotopic liver transplantation (OLT). Approximately 1 month after OLT,...
9.
Ryzko J, Walczak-Sztulpa J, Czubkowski P, Latos-Bielenska A, Kowalski A, Stefanowicz M, et al.
Front Pediatr
. 2022 Mar;
10:834064.
PMID: 35281231
Sensenbrenner syndrome, also known as cranioectodermal dysplasia (CED), is a rare ciliopathy clinically characterized by congenital craniofacial, skeletal, and ectodermal defects. Chronic kidney and liver insufficiency are also present in...
10.
Gehlen J, Giel A, Kollges R, Haas S, Zhang R, Trcka J, et al.
HGG Adv
. 2022 Feb;
3(2):100093.
PMID: 35199045
Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) is the most common congenital malformation of the upper digestive tract. This study represents the first genome-wide association study (GWAS) to identify...