Autori: Sarajlija Adrijan
| Naslov | Acute disseminated encephalomyelitis in children and adolescents-20-year single-center experience in Serbia (Article) |
| Autori | Ostojic Slavica B  Kravljanac Ruzica M Kovacevic Gordana S Vucetic-Tadic Biljana Gazikalovic Slobodan Sarajlija Adrijan
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| Info | SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2022), vol. 150 br. 9-10, str. 544-550 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | Acute disseminated encephalomyelitis in children and adolescents-20-year single-center experience in Serbia (Article) |
| Autori | Ostojic Slavica B Kravljanac Ruzica M Kovacevic Gordana S Vucetic-Tadic Biljana Gazikalovic Slobodan Sarajlija Adrijan
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| Info | SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO, (2022), vol. 150 br. 9-10, str. 544-550 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | A Novel Variant in the LIPA Gene Associated with Distinct Phenotype (Article) |
| Autori | Sarajlija Adrijan Armengol L Maver Ales Kitic Ivana Prokic Dragan Cehic Maja Djuricic MS Peterlin Borut
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| Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2022), vol. 25 br. 1, str. 93-99 |
| Ispravka | Web of Science Članak Elečas Rang časopisa |
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| Naslov | Ambiguous Genitalia and Lissencephaly in a 46,xy Neonate with a Novel Variant of Aristaless Gene (Article) |
| Autori | Basa Mihail I Vukovic Rade M Sarajlija Adrijan Milenkovic Tatjana Djordjevic M Vucetic Biljana Martic Jelena M
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| Info | ACTA ENDOCRINOLOGICA-BUCHAREST, (2021), vol. 17 br. 3, str. - |
| Ispravka | Web of Science Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia (Article) |
| Autori | Raicevic Maja Milenkovic Tatjana Hussain Khalid Djordjevic Maja S Martic Jelena M Todorovic Sladjana Mitrovic Katarina Sarajlija Adrijan Vukovic Rade M
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| Info | EUROPEAN JOURNAL OF PEDIATRICS, (2021), vol. 180 br. 9, str. 2815-2821 |
| 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
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| 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 | Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry (Article; Proceedings Paper) |
| Autori | Molema Femke ... Djordjevic Maja S Sarajlija Adrijan ... (broj koautora 68)
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| Info | JOURNAL OF INHERITED METABOLIC DISEASE, (2019), vol. 42 br. 6, str. 1162-1175 |
| Projekat | Metakids; Erasmus University Medical Center; European Union (EU) [2010 12 01]; Kindness-for-Kids Foundation (Munich, Germany); Dietmar Hopp Foundation (St. Leon-Rot, Germany) |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Decreased plasma L-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment (Article) |
| Autori | Molema Femke ... Djordjevic Maja S Sarajlija Adrijan ... (broj koautora 67)
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| Info | MOLECULAR GENETICS AND METABOLISM, (2019), vol. 126 br. 4, str. 397-405 |
| Projekat | Metakids and Erasmus University Medical Center; European Union within the framework of the Health Programme [2010 12 01]; Kindness-for-Kids Foundation (Munich, Germany); Dietmar Hopp Foundation (St. Leon-Rot, Germany); EU |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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| Naslov | Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disordersA successful strategy for clinical research of rare diseases (Article) |
| Autori | Posset Roland ... Sarajlija Adrijan ... (broj koautora 107)
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| Info | JOURNAL OF INHERITED METABOLIC DISEASE, (2019), vol. 42 br. 1, str. 93-106 |
| Projekat | University of Zurich; Kettering Foundation; Kettering Fund |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science |
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| Naslov | WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material) |
| Autori | Kulikovskaja Leonora Sarajlija Adrijan Savic-Pavicevic Dusanka Lj Dobricic Valerija S Klein Christine Westenberger Ana
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| Info | NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. - |
| Projekat | Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds |
| Ispravka | Web of Science Članak Elečas Rang časopisa Citati: Web of Science Scopus |
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