Piotr Kalicinski
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Explore the profile of Piotr Kalicinski including associated specialties, affiliations and a list of published articles.
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81
Citations
351
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Recent Articles
11.
Alfares B, van der Doef H, Wildhaber B, Casswall T, Nowak G, Delle M, et al.
BMJ Open
. 2023 Jul;
13(7):e066343.
PMID: 37500271
Introduction: Portal vein obstruction (PVO) consists of anastomotic stenosis and thrombosis, which occurs due to a progression of the former. The aim of this large-scale international study is to assess...
12.
Szymanska S, Markiewicz-Kijewska M, Pyzlak M, Karkucinska-Wienckowska A, Ciopinski M, Czubkowski P, et al.
J Clin Med
. 2023 Jul;
12(13).
PMID: 37445304
Introduction: Preclinical models have demonstrated that PD-1 and its ligand programmed death ligand1 (PD-L1) play significant roles in both graft induction and the maintenance of immune tolerance. It has also...
13.
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...
14.
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...
15.
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...
16.
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,...
17.
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...
18.
de Ville de Goyet J, Baumann U, Karam V, Adam R, Nadalin S, Heaton N, et al.
Hepatology
. 2021 Nov;
75(3):634-645.
PMID: 34724224
Background And Aims: The European Liver Transplant Registry (ELTR) has collected data on liver transplant procedures performed in Europe since 1968. Approach And Results: Over a 50-year period (1968-2017), clinical...
19.
Markiewicz-Kijewska M, Kalicinski P, Canizales J, Di Giorgio A, Baumann U, Jorns C, et al.
Children (Basel)
. 2021 Sep;
8(9).
PMID: 34572193
An increasing number of AB0-incompatible (AB0i) liver transplantations (LT) are being undertaken internationally in recent years due to organ shortages and the need for urgent transplantation. The aim of our...
20.
Stefanowicz M, Janowska M, Pawlowska J, Tylki-Szymanska A, Kowalski A, Szymczak M, et al.
Children (Basel)
. 2021 Sep;
8(9).
PMID: 34572178
Transaldolase deficiency (TALDO; OMIM 606003) is a rare inborn autosomal-recessive error of the pentose phosphate pathway. It is an early-onset multisystem disease with dysmorphic features, anaemia, coagulopathy, thrombocytopenia, tubulopathy, hepatosplenomegaly...