Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Antal Nemeth"'
Autor:
Jan C. Kamp, Naomi N. Kappe, Carlos Fernández Moro, Jan Fuge, Mark P. Kuehnel, Sabine Wrenger, Tobias Welte, Bart van Hoek, Danny D. Jonigk, Padmini P. S. J. Khedoe, Pavel Strnad, Mikael Björnstedt, Jan Stolk, Sabina Janciauskiene, Antal Nemeth
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2485 (2023)
PiZZ (Glu342Lys) α1-antitrypsin deficiency (AATD) is characterized by intrahepatic AAT polymerization and is a risk factor for liver disease development in children. The majority of PiZZ children are disease free, hence this mutation alone is not su
Externí odkaz:
https://doaj.org/article/fb5fa1378f564aad8da606ca073c7635
Autor:
Jonas Teng, Anne Elwin, Soley Omarsdottir, Giulia Aquilano, Mireille Vanpee, Antal Nemeth, Afsar Rahbar, Kajsa Bohlin, Björn Fischler, Cecilia Söderberg-Nauclér
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Objectives: To evaluate the prevalence of cytomegalovirus (CMV) infection in preterm infants with cholestasis.Study design: Preterm infants (
Externí odkaz:
https://doaj.org/article/34eac5581e3f45fda7ba1602f8bef08e
Autor:
Simona Hankeova, Jakub Salplachta, Tomas Zikmund, Michaela Kavkova, Noémi Van Hul, Adam Brinek, Veronika Smekalova, Jakub Laznovsky, Feven Dawit, Josef Jaros, Vítězslav Bryja, Urban Lendahl, Ewa Ellis, Antal Nemeth, Björn Fischler, Edouard Hannezo, Jozef Kaiser, Emma Rachel Andersson
Publikováno v:
eLife, Vol 10 (2021)
Organ function depends on tissues adopting the correct architecture. However, insights into organ architecture are currently hampered by an absence of standardized quantitative 3D analysis. We aimed to develop a robust technology to visualize, digita
Externí odkaz:
https://doaj.org/article/b15a162506be45549627228691187bdb
Autor:
Terry G. J. Derks MD, PhD, Antal Nemeth MD, PhD, Katrin Adrian MD, PhD, Henrik Arnell MD, PhD, Ann Bech Roskjær RD, Eva Beijer MD, Sebastiaan te Boekhorst BICT, Carina Heidenborg RD, Marcus Landgren MD ,PhD, Mikael Nilsson RD, Domniki Papadopoulou MD, Katalin Ross RD, Elisabeth Sjöqvist RD, U Stachelhaus-Theimer MD, Ulrike Steuerwald MD, Carl-Johan Törnhage MD, PhD, David A. Weinstein MD, PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 5 (2017)
The third international meeting of the Scandinavian Association for Glycogen Storage Disease focused on hepatic glycogen storage disease and was organized for health-care professionals, patient representatives, and representatives from the industry.
Externí odkaz:
https://doaj.org/article/f081dbb83c644ac6b24016df1062e2d6
Autor:
Jan C. Kamp, Naomi N. Kappe, Carlos Fernández Moro, Jan Fuge, Mark P. Kuehnel, Sabine Wrenger, Tobias Welte, Bart van Hoek, Danny D. Jonigk, Padmini P. S. J. Khedoe, Pavel Strnad, Mikael Björnstedt, Jan Stolk, Sabina Janciauskiene, Antal Nemeth
Publikováno v:
International Journal of Molecular Sciences, 24(3). MDPI
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2485
International Journal of Molecular Sciences
Volume 24
Issue 3
Pages: 2485
PiZZ (Glu342Lys) α1-antitrypsin deficiency (AATD) is characterized by intrahepatic AAT polymerization and is a risk factor for liver disease development in children. The majority of PiZZ children are disease free, hence this mutation alone is not su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e175275b92ababc9fc315d1d2cb23d
http://hdl.handle.net/1887/3590817
http://hdl.handle.net/1887/3590817
Publikováno v:
Acta Paediatrica. 110:141-148
AIM To describe outcome linked to neonatal cholestasis in a defined cohort of very preterm infants. METHODS Population-based retrospective case-control study of preterm infants, gestational age
Autor:
Lut de Baere, Katherine Cowan, Marcus Landgren, Thomas Casswall, Niccolò Seidita, Iris A. Ferrecchia, Alberto Ferriani, Caroline Gimbert, Willemijn F Boonstra, Fabian Peeks, Terry G J Derks, Camilla Carøe, Nerea López Maldonado, Damián Cohen, Jason McMillan, David A. Weinstein, Antal Nemeth, Ute Stachelhaus-Theimer
Publikováno v:
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, 43(2), 279-289. SPRINGER
Journal of Inherited Metabolic Disease, 43(2), 279-289. SPRINGER
The international liver glycogen storage disease (GSD) priority setting partnership (IGSDPSP) was established to identify the top research priorities in this area. The multiphase methodology followed the principles of the James Lind Alliance (JLA) gu
Autor:
Jonas Teng, Linnéa Wickman, Marie Reilly, Antal Nemeth, Björn Fischler, Kajsa Bohlin, Eleonor Tiblad
Publikováno v:
Journal of perinatology : official journal of the California Perinatal Association. 42(6)
Objective To estimate the incidence of cholestasis in neonates with hemolytic disease of the fetus and newborn (HDFN) and investigate risk factors and long-term liver disease. Study design A population-based cohort study of all infants born with HDFN
Publikováno v:
Pediatric Transplantation. 25
Impaired renal function after pediatric (LT) is a recognized problem. Accurate monitoring of (GFR) is imperative to detect declining renal function. GFR can be estimated via s-creatinine and/or p-cystatin C or measured by inulin and or/iohexol cleara
Autor:
Feven Dawit, Simona Hankeova, Vítězslav Bryja, Ewa Ellis, Veronika Smekalova, Emma Andersson, Tomáš Zikmund, Urban Lendahl, Michaela Kavkova, Antal Nemeth, Josef Jaroš, Noémi Van Hul, Adam Brinek, Jozef Kaiser, Björn Fischler, Jakub Salplachta, Jakub Laznovsky, Edouard Hannezo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74c82ee09ace2e69d57492a96e82ba36
https://doi.org/10.7554/elife.60916.sa2
https://doi.org/10.7554/elife.60916.sa2