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Autori: Parezanovic Marina V

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Naslov Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier (Meeting Abstract)
Autori Klaassen Kristel M Djordjevic Maja S Skakic Anita G  Kecman Bozica Parezanovic Marina V Andjelkovic Marina Z Stevanovic Nina  Spasovski Vesna M  Ugrin Milena M Drmanac Radoje Pavlovic Sonja T Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 433-433
Projekat MESTD-RS [451-03-68/2022-14/200042]
Ispravka Web of Science   Elečas   Rang časopisa  
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Naslov Molecular diagnosis of Fabry disease in patients with chronic renal failure of unknown etiology (Meeting Abstract)
Autori Parezanovic Marina V Stojiljkovic Maja M Andjelkovic Marina Z Stevanovic Nina  Spasovski Vesna M  Ugrin Milena M Komazec Jovana Tosic Natasa M  Pavlovic Sonja T Celic Dejan  Vucenovic Jelica Skakic Anita G  
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 432-433
Projekat Takeda GmbH, Serbia
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Naslov Unique pipeline for the assessment of novel genetic variants leads to confirmation of PCD diagnosis (Meeting Abstract)
Autori Stevanovic Nina  Andjelkovic Marina Z Skakic Anita G  Spasovski Vesna M  Stojiljkovic Maja M Parezanovic Marina V Ugrin Milena M Pavlovic Sonja T 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 383-383
Projekat MESTD, Republic of Serbia [451-03-68/2022-14/200042]
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Naslov The Role of Autophagy and Apoptosis in Affected Skin and Lungs in Patients with Systemic Sclerosis (Review)
Autori Spasovski Vesna M  Andjelkovic Marina Z Parezanovic Marina V Komazec Jovana Ugrin Milena M Klaassen Kristel M Stojiljkovic Maja M 
Info INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, (2023), vol. 24 br. 13, str. -
Projekat Ministry of Education, Science, and Technological Development, Republic of Serbia [451-03-47/2023-01/200042]
Ispravka Web of Science   Članak   Elečas   Rang časopisa  
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