Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Zuzana Havlíčeková"'
Autor:
Daniela, Kosorínová, Pavlína, Suchá, Zuzana, Havlíčeková, Marek, Pršo, Pavol, Dvoran, Peter, Bánovčin
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie; 2024, Vol. 79 Issue 4, p213-219, 7p
Publikováno v:
Česko-slovenská pediatrie. 77:353-355
Autor:
Terezia Kráľová, Martina Kostková, Marek Pršo, Zuzana Havlíčeková, Zuzana Michnová, Daniel Čierny
Publikováno v:
Gastroenterologie a hepatologie. 75:335-343
Background: Insulin resistance (IR) plays a key role in the pathogenesis of non-alcoholic fatty liver disease (NAFLD). Hypovitaminosis D is associated with several diseases, including hepatic steatosis and obesity. Vitamin D (VD) affects insulin secr
Autor:
Marek, Pršo, Zuzana, Michnová, Marek, Kozár, Linda, Pršová, Lýdia, Zúbriková, Zuzana, Havlíčeková, Daniela, Kosorínová, Michaela, Murgašová, Kristián, Pršo, Peter, Bánovčin
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie; 2023, Vol. 78 Issue 4, p210-214, 5p
Autor:
Zuzana Havlíčeková, Lýdia Zúbriková, Marek Pršo, Zuzana Michnová, Peter Banovcin, Michaela Murgašová
Publikováno v:
Gastroenterologie a hepatologie. 73:481-487
Autor:
Peter Banovcin, Marek Pršo, Lýdia Zúbriková, Zuzana Michnová, Marek Kozar, Zuzana Havlíčeková, Terézie Kráľová
Publikováno v:
Gastroenterologie a hepatologie. 72:473-478
U zdravej detskej populacie je pocas ultrasonografickeho vysetrenia celkova echogenita peceňoveho parenchýmu porovnateľna s echogenitu kory obliciek ci sleziny. Pri obezite, ako najrizikovejsom faktore vzniku nealkoholovej steatozy pecene (NAFLD),
Autor:
Peter Banovcin, Nadežda Mišovicová, Ľubica Jakušová, Miloš Jeseňák, Jana Kršiaková, Zuzana Havlíčeková
Publikováno v:
Gastroenterologie a hepatologie. 72:152-157
Publikováno v:
Czecho-Slovak Pediatrics / Česko-Slovenská Pediatrie; 2022, Vol. 77 Issue 6, p353-355, 3p
Autor:
Zuzana Havlíčeková, Peter Banovcin, Daniel Danis, Iwar Klimes, Daniela Gasperikova, Jarmila Vojtková, Martina Skopkova, Lucia Valentinova, Miriam Ciljakova, Dalibor Murgas, Renata Szépeová, Juraj Stanik
Publikováno v:
European Journal of Medical Genetics. 59:429-435
Mitchell-Riley syndrome, an autosomal recessive disorder caused by mutations in the RFX6 gene, is defined as a combination of neonatal diabetes mellitus and serious congenital gastrointestinal defects. We describe Mitchell-Riley syndrome in two siste
Autor:
Erik-Oliver Glocker, Jan Rohr, Nadia Saleh, Mehrnaz Mesdaghi, Christian Klemann, Robin Kobbe, Natalie Frede, Renate Abt, Peter Hasselblatt, Sigune Goldacker, Ronnie Chee, Naghi Dara, Mary Buchta, Florian Brinkert, Alla Bulashevska, Aisha Elmarsafy, Birol Öztürk, Paul Thankam, Nermeen Galal, Patrick Gerner, Jutta Hammermann, Mahboubeh M. Kharaghani, Katrin Hübscher, Gunda Ruzaike, Jutte Van Der Werff Ten Bosch, Lida Atarod, Safa Baris, Suranjith L. Seneviratne, Ana Cordeiro, Daniel Kotlarz, Sebastian Zeissig, Horst von Bernuth, Britt-Sabina Petersen, Yvonne Zeissig, Milos Jesenak, Gregor Dückers, Andre Franke, João Farela Neves, Sara Sebnem Kilic, Sally G. Mitton, Dietrich August, Zuzana Havlíčeková, Neslihan Edeer Karaca, T. Ronan Leahy, Bodo Grimbacher, Christoph Klein, Hemant Bhavsar, Moudjahed Saleh Al-Ddafari, Ebru Senol, Carsten Speckmann, Jessica L.R. Restrepo, Daniel Tegtmeyer, Ayca Kiykim, Martin W. Laass, Luis F. Pereira, Elif Karakoc-Aydiner
"Çalışmada 57 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır.” Background: In contrast to adult-onset inflammatory bowel disease (IBD), where many genetic loci have been shown t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1410e31a1932bf36de7f66bbd5614be0
https://hdl.handle.net/20.500.14017/226c4e28-a237-4494-bfb9-0233866baed5
https://hdl.handle.net/20.500.14017/226c4e28-a237-4494-bfb9-0233866baed5