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Browsing by Author Stajic, Natasa

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Issue DateTitleAuthor(s)TypeМ-cat.
2010A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiencyBogdanovic, Radovan M; Draaken, Markus; Toromanovic, Alma; Djordjevic, Maja S; Stajic, Natasa; Ludwig, MichaelArticle
21M21
2012Acute kidney injury in pediatric patients hospitalized in two Serbian tertiary care centers during one yearStajic, Natasa; Bogdanovic, Radovan M; Spasojevic-Dimitrijeva, Brankica B; Ivanisevic, Ivana; Vunjak-Maksimovic, Nevena; Stajevic, Mila S  ; Medjo, Biljana P; Kalanj, Jasna; Rsovac, Snezana; Krunic, Igor;
Peco-Antic, Amira E;
Conference Paper
Mp. category will be shown later
2012Atypical presentation of cystic fibrosis - obese adolescent with hypertension and pseudo-Bartter`s syndromeSovtić, Aleksandar  ; Minic, Predrag  ; Bogdanovic, Radovan; Stajic, Natasa; Rodic, Milan; Markovic-Sovtic, GordanaArticle
23M23
2012COEXISTENCE OF ANTI-GBM ANTIBODIES (Abs) AND MYELOPEROXIDASE-ANCA IN A GIRL WITH PULMONARY RENAL SYNDROME (PRS)Bogdanovic, Radovan M; Minic, Predrag B; Markovic-Lipkovski, Jasmina Z; Stajic, Natasa; Savic, Natasa; Rodic, MilanConference Paper
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2019COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humansKitzler, Thomas M; ...; Bogdanovic, Radovan M; Stajic, Natasa; ...; (broj, koautora 22)Article
21M21
2014Comparison Of The Two Protocols For Management Of The First Febrile Urinary Tract Infection In ChildrenParipovic, Aleksandra; Stajic, Natasa; Putnik, Jovana; Jaksic, Emilija D; Bogdanovic, Radovan MConference Paper
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2023Complicated Urinary Tract Infection in ChildrenParipovic, Aleksandra; Putnik, Jovana; Stajic, NatasaConference Paper
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2008Congenital Nephrotic SyndromeStajic, Natasa; Putnik, Jovana; Paripovic, Aleksandra; Djuricic, Slavisa M; Bogdanovic, Radovan MArticle
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2014Congenital thrombocytopenia with nephritis - The first case of MYH9 related disorder in SerbiaKuzmanović, Miloš  ; Kunishima, Shinji; Putnik, Jovana; Stajic, Natasa; Paripovic, Aleksandra; Bogdanovic, RadovanArticle
23M23
2010Continuous Renal Replacement Therapy (CRRT) in the Neonatal Intensive Care Unit (NICU): 5-Years ExperienceStajic, Natasa; Bogdanovic, Radovan M; Putnik, Jovana; Paripovic, Aleksandra; Jankovic, Borisav Z; Djordjevic, Maja S; Nikitovic-Martic, JelenaConference Paper
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2022Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary TractWu, Chen-Han Wilfred; ...; Stajic, Natasa; ...; (broj, koautora 36)Article
22M22
2015Cryptoccocal Meningitis in the Patient with Systemic Lupus Erythematosus and CD4+Lymphocyte DeficiencyStajic, Natasa; Pasic, Srdjan S; Ostojic, Slavica; Arsic, Valentina S  ; Basta-Jovanovic, Gordana M ; Putnik, Jovana; Paripovic, Aleksandra; Bogdanovic, Radovan MConference Paper
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2022Delineation of the phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy - Alport syndrome and thin basement membrane nephropathyRiedhammer, Korbinian Maria; Braunisch, Matthias C; Comic, Jasmina; Lungu, Adrian; Putnik, Jovana; Milosevski-Lomic, Gordana; Gessner, Michaela; Stajic, Natasa; Patzer, Ludwig; Emini, Nora;
Tasic, Velibor; Hoefele, Julia;
Conference Paper
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2012Dental Abnormalities in Schimke Immuno-osseous DysplasiaMorimoto, Marie; ...; Bogdanovic, Radovan M; ...; Stajic, Natasa; ...; (broj, koautora 36)Article
21aM21a
2017Epidemiological and Clinical Characteristics of Patients with Hemorrhagic Fever with Renal SyndromeStajic, Natasa; Putnik, Jovana; Paripovic, Aleksandra; Bogdanovic, Radovan MConference Paper
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2020Evaluation of carotid intima media thickness in children with idiopathic nephrotic syndromeParipovic, Aleksandra; Stajic, Natasa; Putnik, Jovana; Gazikalovic, Ana; Bogdanovic, Radovan M; Vukomanovic, Vladislav AArticle
23M23
2020Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary NephropathiesRiedhammer, Korbinian Maria; ...; Putnik, Jovana; Stajic, Natasa; ...; (broj, koautora 20)Article
21aM21a
2023Exome sequencing in individuals with congenital anomalies of the kidney and urinary tract (CAKUT): a single-center experienceRiedhammer, Korbinian Maria; Comic, Jasmina; Tasic, Velibor; Putnik, Jovana; Abazi-Emini, Nora; Paripovic, Aleksandra; Stajic, Natasa; Meitinger, Thomas; Nushi-Stavileci, Valbona; Berutti, Riccardo;
Braunisch, Matthias C; Hoefele, Julia;
Article
21M21
2022Exome Sequencing in Individuals with Congenital Anomalies of the Kidney and Urinary Tract (Cakut): a Single-Center ExperienceComic, Jasmina; Riedhammer, Korbinian Maria; Tasic, Velibor; Putnik, Jovana; Abazi-Emini, Nora; Paripovic, Aleksandra; Stajic, Natasa; Nushi-Stavileci, Valbona; Braunisch, Matthias C; Hoefele, JuliaConference Paper
Mp. category will be shown later
2021FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-GlomerulopathyGaram, Nora; ...; Stajic, Natasa; ...; (broj, koautora 68)Article
21M21