Autori: Sarajlija Adrijan
Naslov | Neuroblastoma Occurring in Nijmegen Breakage Syndrome (Article) |
Autori | Djurisic Marina Sarajlija Adrijan ![]() ![]() ![]() ![]() |
Info | JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, (2025), vol. 47 br. 1, str. e74-e76 |
Projekat | Great Northern Children's Hospital, Newcastle upon Tyne |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Phenotypic Variability of Cowden Syndrome Within a Single Family: Impact on Diagnosis, Management and Genetic Counselling (Article) |
Autori | Ilic Nikola A ![]() ![]() ![]() ![]() ![]() ![]() |
Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2024), vol. 27 br. 2, str. 95-100 |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Bisphosphonate Therapy in a Pediatric Case Series with Monostotic Form of Fibrous Dysplasia: A Single-Center Retrospective Analysis of Efficacy and Safety (Meeting Abstract) |
Autori | Ilic Nikola A ![]() ![]() ![]() ![]() |
Info | HORMONE RESEARCH IN PAEDIATRICS, (2024), vol. 97 br. , Suppl. 3, str. 336-336 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study (Article) |
Autori | Ilic Nikola A ![]() ![]() ![]() ![]() |
Info | GENES, (2024), vol. 15 br. 11, str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Treatment of RAF1-Related Biventricular Hypertrophy and Double Chamber Right Ventricle by MEK Inhibition Using Trametinib (Letter; Early Access) |
Autori | Krasic Stasa D ![]() ![]() ![]() ![]() |
Info | INDIAN JOURNAL OF PEDIATRICS, (2024), vol. br. , str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa Citati: |
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Naslov | Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity? (Article) |
Autori | Ilic Nikola A ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
Info | GENES, (2024), vol. 15 br. 6, str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21 (Article) |
Autori | Paripovic Aleksandra Maver Ales Stajic Natasa Putnik Jovana ![]() ![]() ![]() |
Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 2, str. 59-64 |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Age-specific causes of upper gastrointestinal bleeding in children (Review) |
Autori | Kocic Marija Rasic Petar ![]() ![]() |
Info | WORLD JOURNAL OF GASTROENTEROLOGY, (2023), vol. 29 br. 47, str. - |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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Naslov | Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region (Meeting Abstract) |
Autori | Perovic Dijana ![]() ![]() ![]() ![]() ![]() ![]() |
Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2023), vol. 31 br. , Suppl. 1, str. 267-268 |
Ispravka | Web of Science Elečas Rang časopisa |
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Naslov | Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency (Article) |
Autori | Parezanovic M Ilic Nina Ostojic Slavica B ![]() ![]() |
Info | BALKAN JOURNAL OF MEDICAL GENETICS, (2023), vol. 26 br. 1, str. 63-67 |
Ispravka | Web of Science Članak Elečas Rang časopisa |
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