Autori: Kecman Bozica
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 | 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 ![]() ![]() |
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 ![]() ![]() ![]() |
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 | 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 ![]() |
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 ![]() ![]() |
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 ![]() ![]() ![]() ![]() |
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 ![]() ![]() |
Info | BLOOD CELLS MOLECULES AND DISEASES, (2018), vol. 68 br. , str. 109-111 |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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Naslov | Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency (Letter) |
Autori | Sarajlija Adrijan ![]() |
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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