PhD Marija Meznarič [04905]

1. MORA, Marina, ANGELINI, Corrado, BIGNAMI, Fabrizia, BODIN, Anne-Mary, CRIMI, Marco, DI DONATO, Jeanne-Hélène, FELICE, Alex, JAEGER, Cécile, MEZNARIČ, Marija, et al. TheEuroBioBank Network : 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases. EJHG. European journal of human genetics. Sep. 2015, vol. 23, iss. 9, str. 1116-1123, ilustr. ISSN 1018-4813. DOI: 10.1038/ejhg.2014.272. [COBISS.SI-ID 31776473]

2. KALKO, Sabina Graciela, PACO, Sonia, JOU, Cristina, ANGELS RODRÍGUEZ, Maria, MEZNARIČ, Marija, ROGAČ, Mihael, JEKOVEC-VRHOVŠEK, Maja, SCIACCO, Monica, MOGGIO, Maurizio, FAGIOLARI, Gigiola, et al. Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies. BMC genomics. 2014, vol. 15. ISSN 1471-2164. http://www.biomedcentral.com/1471-2164/15/91/abstract, DOI: 10.1186/1471-2164-15-91. [COBISS.SI-ID 31139801]

3. ŠTIMPFEL, Martin, SKUTELLA, Thomas, CVJETIČANIN, Branko, MEZNARIČ, Marija, DOVČ, Peter, NOVAKOVIĆ, Srdjan, ŠKERL, Petra, VRTAČNIK-BOKAL, Eda, VIRANT-KLUN, Irma. Isolation, characterization and differentiation of cells expressing pluripotent/multipotent markers from adult human ovaries. Cell and tissue research. Nov. 2013, vol. 354, no. 2, str. 593-607, ilustr. ISSN 0302-766X. DOI: 10.1007/s00441-013-1677-8. [COBISS.SI-ID 30679001]

4. ROGAČ, Mihael, MEZNARIČ, Marija, ZEVIANI, Massimo, SPERL, Wolfgang, NEUBAUER, David. Functional outcome of children with mitochondrial diseases. Pediatric neurology. [Print ed.]. 2011, vol. 44, no. 5, str. 340-346, graf. prikazi, tabele. ISSN 0887-8994. DOI: 10.1016/j.pediatrneurol.2010.12.004. [COBISS.SI-ID 28533977]

5. SPINAZZOLA, A., INVERNIZZI, F., CARRARA, F., LAMANTEA, E., DONATI, A., DIROCCO, M., GIORDANO, I., MEZNARIČ, Marija, BARUFFINI, E., FERRERO, I., ZEVIANI, M. Clinical and molecular features of mitochondrial DNA depletion syndromes. Journal of inherited metabolic disease. 2009, letn. 32, št. 2, str. 143-158. ISSN 0141-8955. DOI: 10.1007/s10545-008-1038-z. [COBISS.SI-ID 26137049]

6. MEZNARIČ, Marija, KRALJ, Eduard, ANGELINI, Corrado, FANIN, Marina, TRINKAUS, Darinka. Cardiomyopathy in a patient with limb-girdle muscular dystrophy type 2D : pathomorphological aspects. In: BALAŽIC, Jože (ed.). Proceedings of the 17th International Meeting on Forensic Medicine Alpe-Adria-Panonia, Portorož, Slovenia, May 7-10, 2008. [Shannon]: Elsevier, 2009. Letn. 1, št. 1, suppl., str. 58-62. Forensic Science International Supplement Series, vol. 1, iss. 1. ISSN 1875-1741. [COBISS.SI-ID 26734809]

7. PALMIERI, Luigi, ALBERIO, Simona, PISANO, Isabella, LODI, Tiziana, MEZNARIČ, Marija, ZIDAR, Janez, SANTORO, Antonella, et al. Complete loss-of-function of the heart/muscle-specific adenine nucleotide translocator is asoociated with mitochondrial myopathy and cardiomyopathy. Human molecular genetics. 2005, letn. 14, št. 20, str. 3079-3088. ISSN 0964-6906. [COBISS.SI-ID 20435161]

8. FANIN, Marina, NASCIMBENI, Anna Chiara, FULIZIO, Luigi, TREVISAN, Carlo Pietro, MEZNARIČ, Marija, ANGELINI, Corrado. Loss of calpain-3 autoacatalytic activity in LGMD2A patients with normal protein expression. The American journal of pathology. 2003, letn. 163, št. 5, str. 1929-1936. ISSN 0002-9440. [COBISS.SI-ID 16846809]

9. PETERLIN, Borut, ZIDAR, Janez, MEZNARIČ, Marija, ZUPANČIČ, N... Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia. Clinical genetics. 1997, let. 51, št. 2, str. 94-97. ISSN 0009-9163. [COBISS.SI-ID 7491801]

10. MEZNARIČ, Marija, PETERLIN, Borut, ZIDAR, Janez, et al. Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele. European journal of neurology. 2011, vol. 18, issue 7, str. 1021-1023. ISSN 1351-5101. DOI: 10.1111/j.1468-1331.2010.03240.x. [COBISS.SI-ID 28533721]