Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Zaklina Sterjova-Markovska"'
Autor:
Vladimir Pushevski, Aleksandra Canevska, Zaklina Sterjova Markovska, Ana Marija Shpishikj Pushevska, Mimoza Milenkova, Irena Rambabova Busletik
Publikováno v:
Journal of Morphological Sciences. 6:98-103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e80ba6963e728f39c73d239d58614554
https://doi.org/10.55302/jms2361098p
https://doi.org/10.55302/jms2361098p
Autor:
Irena Rambabova-Bushljetik, Pavlina Dzekova-Vidimliski, Vlatko Karanfilovski, Zaklina Sterjova-Markovska, Fadil Cana, Oliver Bushljetikj, Svetlana Balkanov, Aleksandra Kapedanovska-Nestorovska, Aleksandar Dimovski
Publikováno v:
PRILOZI. 43:61-66
Carnitine palmitoyltransferase II deficiency (CPT II) is an autosomal recessive inherited disorder of long-chain fatty acid oxidation in the mitochondrial matrix, resulting in an inability to utilize fat for energy in cells. The most frequent myopath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e43a8cc9e259ce50f2ae9049eebb7bf0
https://doi.org/10.2478/prilozi-2022-0037
https://doi.org/10.2478/prilozi-2022-0037
Autor:
Irena, Rambabova-Bushljetik, Pavlina, Dzekova-Vidimliski, Vlatko, Karanfilovski, Zaklina, Sterjova-Markovska, Fadil, Cana, Oliver, Bushljetikj, Svetlana, Balkanov, Aleksandra, Kapedanovska-Nestorovska, Aleksandar, Dimovski
Publikováno v:
Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki)REFERENCES. 43(3)
Carnitine palmitoyltransferase II deficiency (CPT II) is an autosomal recessive inherited disorder of long-chain fatty acid oxidation in the mitochondrial matrix, resulting in an inability to utilize fat for energy in cells. The most frequent myopath
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::660c22c4e61bc7ef41aff596dbdb2068
https://pubmed.ncbi.nlm.nih.gov/36473042
https://pubmed.ncbi.nlm.nih.gov/36473042