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Autori: Andjelkovic Marina Z

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Naslov Costello Syndrome Associated With Somatic Mosaicism of Rare p.Gly13Asp HRAS Variant: Expanding the Phenotypic Spectrum (Article)
Autori Lalosevic Jovan  Djordjevic Katarina  Gajic-Veljic Mirjana  Pavlovic Sonja  Gasic Vladimir V  Andjelkovic Marina Z  Nikolic Milos 
Info MOLECULAR GENETICS & GENOMIC MEDICINE, (2026), vol. 14 br. 9, str. -
Projekat Ministarstvo Prosvete, Nauke i Tehnoloscaron;kog Razvoja [175065]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov The Diagnostic Journey from Rhabdomyolysis to Myopathy with Tubular Aggregates: A Family-Based Case Report and Review of the Literature (Review)
Autori Ostojic Slavica  Milenkovic Sanja  Pavlovic Sonja  Kovacevic Gordana  Petrovic Gordana  Paripovic Aleksandra  Sarajlija Adrijan  Andjelkovic Marina Z  Gasic Vladimir  Radivojevic Danijela 
Info PEDIATRIC REPORTS, (2026), vol. 18 br. 4, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3 (Review)
Autori Kravljanac Ruzica M  Klaassen Kristel M  Oparnica Vladimir  Vucetic-Tadic Biljana  Andjelkovic Marina Z  Skakic Anita G  Stankovic Sara S  Stojiljkovic Maja M 
Info DISEASES, (2026), vol. 14 br. 5, str. -
Projekat Ministry of Science, Technological Development and Innovation of the Republic of Serbia [451-03-33/2026-03/200042]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield (Article)
Autori Ostojic Slavica B  Kovacevic Gordana S  Ilic Nikola A  ...  Andjelkovic Marina Z  Lalic Tanja  Miskovic Marijana  Klaassen-Ljubicic Kristel M  Marjanovic Irena M  Paripovic Aleksandra  Basa Mihail I  Vukomanovic Vladislav A  Krstic Jovana  Adamovic Milica  Sovtic Aleksandar D  Sarajlija Adrijan 
Info INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, (2026), vol. 27 br. 9, str. -
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov Behçet's syndrome-like features revealing myelodysplastic syndrome with TP53 mutation: a case report (Article)
Autori Pesic Andrej  Ljubicic Jelena  Todorovic-Balint Milena R  Klaassen Kristel M  Andjelkovic Marina Z  Pavlovic Sonja T  Stojanovic Maja R 
Info FRONTIERS IN IMMUNOLOGY, (2026), vol. 17 br. , str. -
Projekat Ministarstvo Prosvete, Nauke i Tehnoloscaron;kog Razvoja
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa   Citati:
Naslov First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review (Review)
Autori Djordjevic-Milosevic Maja  Skakic Anita G  Andjelkovic Marina Z  Delgado-Vega Angelica Maria  Thonberg Hakan  Klaassen Kristel M  Komazec Jovana  Kecman Bozica  Jocic Nikola  Bjorck Erik  Lindstrand Anna  Stojiljkovic Maja M 
Info DISEASES, (2026), vol. 14 br. 3, str. -
Projekat European Commission, Horizon Europe Project BRIDGING-RD, HORIZON-WIDERA-2023-ACCESS-02 [101160079]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
Naslov Thalassemia syndromes in Serbia:the importance of genetic (re)analysis (Meeting Abstract)
Autori Ugrin Milena M  Komazec Jovana  Klaassen Kristel M  Skakic Anita G  Andjelkovic Marina Z  Spasovski Vesna M  Stevanovic Nina  Parezanovic Marina V  Stankovic Sara S  Jocic Nikola  Pavlovic Sonja T  Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 393-393
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Applications of the new tool: VUS Notifier (Meeting Abstract)
Autori Domazet Milan  Ugrin Milena M  Andjelkovic Marina Z  Klaassen Kristel M  Skakic Anita G  Komazec Jovana  Spasovski Vesna M  Todorovic Sasa  Stojiljkovic Maja M 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 888-888
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Unravelling phenylalanine-induced neuronal dysfunction: transcriptome analysis of NT2-derived neurons highlights neurite impairment and synaptic connectivity (Meeting Abstract)
Autori Stankovic Sara S  Lazic Andrijana  Parezanovic Marina V  Andjelkovic Marina Z  Ugrin Milena M  Stevanovic Milena J  Pavlovic Sonja T  Stojiljkovic Maja M  Klaassen Kristel M 
Info EUROPEAN JOURNAL OF HUMAN GENETICS, (2025), vol. 33 br. , Suppl. 1, str. 715-715
Ispravka ISI/Web of Science   Elečas   Rang časopisa  
Naslov Phenylbutyric Acid Modulates Apoptosis and ER Stress-Related Gene Expression in Glycogen Storage Disease Type Ib In Vitro Model (Article)
Autori Parezanovic Marina V  Stevanovic Nina  Andjelkovic Marina Z  Ugrin Milena M  Pavlovic Sonja T  Stojiljkovic Maja M  Skakic Anita G 
Info MOLECULAR GENETICS & GENOMIC MEDICINE, (2025), vol. 13 br. 1, str. -
Projekat Science Fund of the Republic of Serbia [6999]
Ispravka ISI/Web of Science   Članak   Elečas   Rang časopisa  
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