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Balint Nagy

Showing results (41-50 of 44) with videos related to

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Scientific Reports|July 19, 2024
Validation of a novel, low-fidelity virtual reality simulator and an artificial intelligence assessment approach for peg transfer laparoscopic trainingPeter Zoltan Bogar, Mark Virag, Matyas Bene, et al.
Human Molecular Genetics|July 24, 2019
Underlying molecular alterations in human dihydrolipoamide dehydrogenase deficiency revealed by structural analyses of disease-causing enzyme variantsEszter Szabo, Piotr Wilk, Balint Nagy, et al.
Virchows Archiv : an International Journal of Pathology|September 16, 2008
Placental protein 13 (galectin-13) has decreased placental expression but increased shedding and maternal serum concentrations in patients presenting with preterm pre-eclampsia and HELLP syndromeNandor Gabor Than, Omar Abdul Rahman, Rita Magenheim, et al.
European Journal of Human Genetics : EJHG|July 14, 2016
Rare novel variants in the ZIC3 gene cause X-linked heterotaxyAimee D C Paulussen, Anja Steyls, Jo Vanoevelen, et al.
Pageof 5

Showing results (41-50 of 44) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 44 results.
Scientific Reports|July 19, 2024
Validation of a novel, low-fidelity virtual reality simulator and an artificial intelligence assessment approach for peg transfer laparoscopic trainingPeter Zoltan Bogar, Mark Virag, Matyas Bene, et al.
Human Molecular Genetics|July 24, 2019
Underlying molecular alterations in human dihydrolipoamide dehydrogenase deficiency revealed by structural analyses of disease-causing enzyme variantsEszter Szabo, Piotr Wilk, Balint Nagy, et al.
Virchows Archiv : an International Journal of Pathology|September 16, 2008
Placental protein 13 (galectin-13) has decreased placental expression but increased shedding and maternal serum concentrations in patients presenting with preterm pre-eclampsia and HELLP syndromeNandor Gabor Than, Omar Abdul Rahman, Rita Magenheim, et al.
European Journal of Human Genetics : EJHG|July 14, 2016
Rare novel variants in the ZIC3 gene cause X-linked heterotaxyAimee D C Paulussen, Anja Steyls, Jo Vanoevelen, et al.
Pageof 5