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Autori: Kecman Bozica

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Naslov Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease (Meeting Abstract)
Autori Maric Nina Kecman Bozica Ostojic Slavica B  
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1030-1031
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Naslov Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease (Meeting Abstract)
Autori Maric Nina Kecman Bozica Ostojic Slavica B  
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2024), vol. 32 br. , Suppl. 2, str. 1030-1031
Ispravka Web of Science   Elečas   Rang časopisa  
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Naslov Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies (Article; Early Access)
Autori Andjelkovic Marina Z Klaassen Kristel M Skakic Anita G  Marjanovic Irena M  Kravljanac Ruzica M Djordjevic Maja S Vucetic-Tadic Biljana Kecman Bozica Pavlovic Sonja T Stojiljkovic Maja M 
Info MOLECULAR DIAGNOSIS & THERAPY, (2024), vol. br. , str. -
Projekat Ministry of Science, Technological Development and Innovations Republic of Serbia [451-03-66/2024-03/200042]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati:
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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]
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Naslov Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire (Article)
Autori Gruenert Sarah C ... Djordjevic-Milosevic Maja ... Kecman Bozica ... (broj koautora 64) 
Info GENETICS IN MEDICINE, (2022), vol. 24 br. 8, str. 1781-1788
Projekat [739543]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier (Article)
Autori Klaassen Kristel M Djordjevic Maja S Skakic Anita G  Kecman Bozica Drmanac Radoje Pavlovic Sonja T Stojiljkovic Maja M 
Info MOLECULAR GENETICS AND METABOLISM REPORTS, (2021), vol. 29 br. , str. -
Projekat Ministry of Education, Science and Technological Development Republic of Serbia [451-03-68/2020-14/200042]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib (Article)
Autori Sarajlija Adrijan  Djordjevic Maja S Kecman Bozica Skakic Anita G  Pavlovic Sonja T Pasic Srdjan S Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF MEDICAL GENETICS, (2020), vol. 63 br. 3, str. -
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [III41004]; European Commission Joint Research Centre [EU-FP7-REGPOT-316088]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants (Article)
Autori Skakic Anita G  Djordjevic Maja S Sarajlija Adrijan  Klaassen Kristel M Tosic Natasa M  Kecman Bozica Ugrin Milena M Spasovski Vesna M  Pavlovic Sonja T Stojiljkovic Maja M 
Info CLINICAL GENETICS, (2018), vol. 93 br. 2, str. 350-355
Projekat Ministry of Education, Science and Technological Development, Republic of Serbia [III41004]; European Commission [EU-FP7-REGPOT-316088]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Appendiceal involvement in a patient with Gaucher disease (Article)
Autori Kocic Marija Djuricic Slavisa M  Djordjevic Maja S Savic Djordje Kecman Bozica Sarajlija Adrijan  
Info BLOOD CELLS MOLECULES AND DISEASES, (2018), vol. 68 br. , str. 109-111
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Naslov Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency (Letter)
Autori Sarajlija Adrijan  Magner Martin Djordjevic Maja S Kecman Bozica Grujic Blagoje Tesarova Marketa Minic Predrag B 
Info CONGENITAL ANOMALIES, (2017), vol. 57 br. 2, str. 64-65
Projekat [RVO-VFN64165/2012]; [PRVOUK P24/LF1/3]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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