Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Antonija Ruzic Barsic"'
Autor:
Lucija Ruzman, Ivana Kolic, Jelena Radic Nisevic, Antonija Ruzic Barsic, Ingrid Skarpa Prpic, Igor Prpic
Publikováno v:
Upsala Journal of Medical Sciences, Vol 124, Iss 4, Pp 273-277 (2019)
Background: Mitochondrial disorders are heterogeneous clinical syndromes caused by defective activity in the mitochondrial respiratory chain, resulting in a faulty oxidative phosphorylation system. These inherited disorders are individually rare, and
Externí odkaz:
https://doaj.org/article/41b2b4f82f384be581de0f99110d3ece
Autor:
I. Prpić, Ivana Kolić, Antonija Ruzic Barsic, Igor Prpić, Jelena Radić Nišević, Lucija Ruzman
Publikováno v:
Upsala Journal of Medical Sciences
Upsala Journal of Medical Sciences, Vol 124, Iss 4, Pp 273-277 (2019)
Upsala Journal of Medical Sciences, Vol 124, Iss 4, Pp 273-277 (2019)
Background: Mitochondrial disorders are heterogeneous clinical syndromes caused by defective activity in the mitochondrial respiratory chain, resulting in a faulty oxidative phosphorylation system. These inherited disorders are individually rare, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::821cf3b9a3c5920b04b80c5571bd90c1
https://doi.org/10.1080/03009734.2019.1670297
https://doi.org/10.1080/03009734.2019.1670297
Publikováno v:
Polish Journal of Radiology
Summary Background Internal carotid artery agenesis is a rare anomaly that can be clinically asymptomatic. Klippel-Feil syndrome is a skeletal malformation characterized by vertebral fusion. Presence of postaxial polydactyly is suggestive of an under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::139b6b0552b00123084e100def58ac90
http://europepmc.org/articles/PMC4357484
http://europepmc.org/articles/PMC4357484