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Dr Nataša Stajić

Načelnik Odeljenja za ispitivanje i lečenje bolesti bubrega i mokraćnih puteva

Biografija

Rođena 21.8.1968. u Vranju, Srbija

Školovanje

  • Diploma doktora medicine 14.6.1994. godine na Medicinskom fakultetu u Beogradu – prosečna ocena 9.13.
  • Diploma specijaliste pedijatrije 2.6.2000. godine na Medicinskom fakultetu u Beogradu – ocena odličan.
  • Specijalističke akademske studije – modul nefrologija 16.9. 2016., prosečna ocena 9.55.
  • Završni rad „Akutno oštećenje bubrega u kod bolesnika u tercijarnim pedijatrijskim ustanovama“ – ocena 10.

Radno iskustvo

  • Lekar specijalista pedijatrije na Odeljenju za lečenje bolesti bubrega i mokraćnih puteva od 2000 – 2014.
  • Načelnik Odeljenja za lečenje bolesti bubrega i mokraćnih puteva od 2014.

Usavršavanja u inostranstvu

  • First International Conference of Critical Care Nephrology in Children,London
    Jul 2023 Hands-on pCRRT course
  • 9th SEPNWG IPNA course, Brijuni Oct 2021 Online teaching course
  • Study designs, health metrics and Sep 2021 Three-day Oxford online course
  • Pediatric renovascular education days webinar Oct 2020 Online two-day course, London 8th Southeastern European Pediatric Nephrology Working Group Meeting
  • IPNA/ESPN teaching course, Belgrade, Serbia, Sep 2019
  • How to become your local expert in nephro-genetics, Belgrade, Serbia, European Reference Kidney Network Oct 2018
  • Orlando Pediatric Renal Replacement Therapy (pCRRT) Conference 2017 Aug 2017 Hands-on pCRRT course
  • London Pediatric Renal Replacement Therapy (pCRRT) Conference 20115 Jul 2015 Hands-on pCRRT course
  • Gostujući lekar od avgusta 2003 – decembra 2003.
    Children’s Memorial Hospital, CHICAGO
    Internship in Maintenance Dialysis, Office based consultative pediatric kidney diseases, Kidney transplantation, and in-patient pediatric kidney diseases, Children’s Memorial Hospital, Feinberg School of Medicine, Northwestern University Chicago, USA (Prof C. Langman)

Status u nastavi u visokoškolskim ustanovama

Klinički asistent

Članstvo i/ili rukovođenje u profesionalnim udruženjima i organizacijama

  • International Pediatric Nephrology Association
  • European Society for Pediatric Nephrology
  • International Society of Nephrology
  • Predsednik Pedijatrijskog aktiva Nefrološke sekcije SLD-a 2022

Oblast profesionalnog interesovanja i istraživanja

Nefrogenetika, sistemski eritemski lupus, tubulopatije

Nagrade i priznanja

Lična satisfakcija 😊

Reference od značaja

  1. Garam N, Cserhalmi M, Prohászka Z, Szilágyi Á, Veszeli N, Szabó E, Uzonyi B, Iliás A, Aigner C, Schmidt A, Gaggl M, Sunder-Plassmann G, Bajcsi D, Brunner J, Dumfarth A, Cejka D, Flaschberger S, Flögelova H,Haris Á, Hartmann Á, Heilos A, Mueller T, Rusai K, Arbeiter K, Hofer J,Jakab D, Sinkó M, Szigeti E, Bereczki C, Janko V, Kelen K, Reusz GS, Szabó AJ, Klenk N, Kóbor K, Kojc N, Knechtelsdorfer M, Laganovic M, Lungu AC,Meglic A, Rus R, Kersnik Levart T, Macioniene E, Miglinas M, PawłowskaA, Stompór T, Podracka L, Rudnicki M, Mayer G, Rysava R, Reiterova J, Saraga M, Seeman T, Zieg J, Sládková E, Stajic N, Szabó T, Capitanescu A, Stancu S, Tisljar M, Galesic K, Tislér A, Vainumäe I, Windpessl M, Zaoral T, Zlatanova G, Józsi M, Csuka D. FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex- Mediated Membranoproliferative Glomerulonephritis and C3- Glomerulopathy. Front Immunol. 2021 Sep 10;12:720183. doi: 10.3389/fimmu.2021.720183. PMID: 34566977; PMCID: PMC8461307.
  2. Zheng B, Seltzsam S, Wang C, Schierbaum L, Schneider S, Wu CW, Dai R, Connaughton DM, Nakayama M, Mann N, Stajic N, Mane S, Bauer SB, Tasic V, Nam HJ, Shril S, Hildebrandt F. Whole-exome sequencing identifies FOXL2, FOXA2 and FOXA3 as candidate genes formonogenic congenital anomalies of the kidneys and urinary tract. Nephrol Dial Transplant. 2022 Sep 22;37(10):1833-1843. doi: 10.1093/ndt/gfab253. PMID: 34473308; PMCID: PMC9755999.
  3. Bjornstad EC, Krallman KA, Askenazi D, Zappitelli M, Goldstein SL, Basu RK; SPARC Investigators. Preliminary Assessment of Acute KidneyInjury in Critically Ill Children Associated with SARS-CoV-2 Infection: AMulticenter Cross-Sectional Analysis. Clin J Am Soc Nephrol. 2021 Mar8;16(3):446-448. doi: 10.2215/CJN.11470720. Epub 2020 Nov 3. PMID:33144276; PMCID: PMC8011012.
  4.  Basu RK, Kaddourah A, Goldstein SL; AWARE Study Investigators. Assessment of a renal angina index for prediction of severe acute kidney injury in critically ill children: a multicentre, multinational,prospective observational study. Lancet Child Adolesc Health. 2018 Feb;2(2):112-120. doi: 10.1016/S2352-4642(17)30181-5. PMID: 30035208; PMCID: PMC6053052.
  5. Kezić A, Stajic N, Thaiss F. Innate Immune Response in Kidney Ischemia/Reperfusion Injury: Potential Target for Therapy. J ImmunolRes. 2017;2017:6305439. doi: 10.1155/2017/6305439. Epub 2017 Jun 6.PMID: 28676864; PMCID: PMC5476886.
  6. Peco-Antić A, Stajić N, Krstić Z, Bogdanović R, Miloševski-Lomić G, Đukić M, Paripović D. Associated extrarenal vascular diseases may complicate the treatment and outcome of renovascular hypertension. Acta Paediatr. 2016 Jan;105(1):e35-41. doi: 1111/apa.13229. Epub 2015 Nov 4. PMID: 26437121.
  7. Bogdanović R, Kuburović V, Stajić N, Mughal SS, Hilger A, Ninić S, Prijić S, Ludwig M. Liddle syndrome in a Serbian family and literature review of underlying mutations. Eur J Pediatr. 2012 Mar;171(3):471-8. doi: 10.1007/s00431-011-1581-8. Epub 2011 Sep 29. PMID: 21956615.
  8.  Stajić N, Putnik J, Paripović A, Bogdanović R. Transient pseudohypoaldosteronism. Srp Arh Celok Lek. 2011 Jan-Feb;139(1-2): 37-43. Serbian. doi: 10.2298/sarh1102037s. PMID: 21568081.
  9. Bogdanović R, Draaken M, Toromanović A, Dordević M, Stajić N, Ludwig M. A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency. Pediatr Nephrol. 2010 Nov;25 (11):2363-8. doi: 10.1007/s00467-010-1615-x. Epub 2010 Aug 1. PMID: 20680351.
  10. Hunter KB, Lücke T, Spranger J, Smithson SF, Alpay H, André JL, Asakura Y, Bogdanovic R, Bonneau D, Cairns R, Cransberg K, Fründ S,Fryssira H, Goodman D,  Helmke K, Hinkelmann B, Lama G, Lamfers P, Loirat C, Majore S, Mayfield C, Pontz BF, Rusu C, Saraiva JM, Schmidt B, Shoemaker L, Sigaudy S, Stajic N, Taha D, Boerkoel CF. Schimke immunoosseous dysplasia: defining skeletal features. Eur J Pediatr. 2010 Jul;169(7):801-11. doi: 10.1007/s00431-009-1115-9. Epub 2009 Dec 15. PMID: 20013129; PMCID: PMC2876264.
  11. Stajić N, Putnik J, Paripović A, Djurić S, Bogdanović R. Congenital nephrotic syndrome. Srp Arh Celok Lek. 2008 Dec;136

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