Antal Dezsofi
Overview
Explore the profile of Antal Dezsofi including associated specialties, affiliations and a list of published articles.
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Articles
58
Citations
630
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Recent Articles
1.
Boros K, Veres G, Pinter H, Richter E, Cseh A, Dezsofi A, et al.
Front Pediatr
. 2024 Dec;
12:1204639.
PMID: 39629099
Introduction: Sarcopenia is associated with poor clinical outcomes in chronic diseases. Our study aimed to characterize body composition (BC) parameters in patients with inflammatory bowel disease (IBD) and compare skeletal...
2.
Hansen B, Vandriel S, Vig P, Garner W, Mogul D, Loomes K, et al.
Hepatology
. 2023 Dec;
79(6):1279-1292.
PMID: 38146932
Background And Aims: Alagille syndrome (ALGS) is characterized by chronic cholestasis with associated pruritus and extrahepatic anomalies. Maralixibat, an ileal bile acid transporter inhibitor, is an approved pharmacologic therapy for...
3.
Lenz D, Schlieben L, Shimura M, Bianzano A, Smirnov D, Kopajtich R, et al.
Hepatology
. 2023 Nov;
79(5):1075-1087.
PMID: 37976411
Background And Aims: Pediatric acute liver failure (PALF) is a life-threatening condition. In Europe, the main causes are viral infections (12%-16%) and inherited metabolic diseases (14%-28%). Yet, in up to...
4.
Molnar M, Szlepak T, Csurke I, Loth S, Kaposzta R, Erdos M, et al.
Front Genet
. 2023 Jun;
14:1158108.
PMID: 37347058
Acid sphingomyelinase deficiency (ASMD) is an autosomal recessive disease caused by biallelic pathogenic variants in the sphingomyelin phosphodiesterase-1 () gene. Acid sphingomyelinase deficiency is characterized by a spectrum of disease...
5.
Beres N, Szentannay J, Kalman A, Sesztak T, Varkonyi I, Halasz J, et al.
JPGN Rep
. 2023 May;
2(1):e045.
PMID: 37206932
No abstract available.
6.
Felzen A, van Wessel D, Gonzales E, Thompson R, Jankowska I, Shneider B, et al.
JHEP Rep
. 2023 Jan;
5(2):100626.
PMID: 36687469
Background & Aims: Bile salt export pump (BSEP) deficiency frequently necessitates liver transplantation in childhood. In contrast to two predicted protein truncating mutations (PPTMs), homozygous p.D482G or p.E297G mutations are...
7.
Kadenczki O, Dezsofi A, Cseh A, Szucs D, Vass N, Nemes E, et al.
Int J Environ Res Public Health
. 2022 Dec;
19(23).
PMID: 36498163
Malnutrition and inflammatory bowel disease (IBD) are interrelated conditions. Our aim was to assess the prevalence of malnutrition, to compare anthropometric parameters in the evaluation of nutritional status in pediatric...
8.
Vandriel S, Li L, She H, Wang J, Gilbert M, Jankowska I, et al.
Hepatology
. 2022 Aug;
77(2):512-529.
PMID: 36036223
Background And Aims: Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real-world data are lacking. This study aimed...
9.
Meinel K, Szabo D, Dezsofi A, Pohl S, Strini T, Greimel T, et al.
Front Pediatr
. 2022 May;
10:903360.
PMID: 35633951
Objectives: The exact etiology of pruritus in chronic cholestasis is unknown. Pruritus intensity does not correlate with common biochemical indices and there is a lack of biomarkers guiding diagnosis and...
10.
Fischler B, Czubkowski P, Dezsofi A, Liliemark U, Socha P, Sokol R, et al.
J Clin Med
. 2022 Feb;
11(4).
PMID: 35207217
Cytomegalovirus (CMV) infection has been suggested to be of importance for the development and outcome of biliary atresia (BA). However, most data are only available from single centre studies. We...