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Items: 1 to 50 of 101

1.

COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.

Kitzler TM, Schneider R, Kohl S, Kolvenbach CM, Connaughton DM, Dai R, Mann N, Nakayama M, Majmundar AJ, Wu CW, Kari JA, El Desoky SM, Senguttuvan P, Bogdanovic R, Stajic N, Valivullah Z, Lek M, Mane S, Lifton RP, Tasic V, Shril S, Hildebrandt F.

Hum Genet. 2019 Oct;138(10):1105-1115. doi: 10.1007/s00439-019-02042-4. Epub 2019 Jun 22.

PMID:
31230195
2.

Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract.

van der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, Hwang DY, Schulz J, Braun DA, Schmidt JM, Schapiro D, Schneider R, Warejko JK, Daga A, Majmundar AJ, Tan W, Jobst-Schwan T, Hermle T, Widmeier E, Ashraf S, Amar A, Hoogstraaten CA, Hugo H, Kitzler TM, Kause F, Kolvenbach CM, Dai R, Spaneas L, Amann K, Stein DR, Baum MA, Somers MJG, Rodig NM, Ferguson MA, Traum AZ, Daouk GH, Bogdanović R, Stajić N, Soliman NA, Kari JA, El Desoky S, Fathy HM, Milosevic D, Al-Saffar M, Awad HS, Eid LA, Selvin A, Senguttuvan P, Sanna-Cherchi S, Rehm HL, MacArthur DG, Lek M, Laricchia KM, Wilson MW, Mane SM, Lifton RP, Lee RS, Bauer SB, Lu W, Reutter HM, Tasic V, Shril S, Hildebrandt F.

J Am Soc Nephrol. 2018 Sep;29(9):2348-2361. doi: 10.1681/ASN.2017121265. Epub 2018 Aug 24.

3.

Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment.

Ashraf S, Kudo H, Rao J, Kikuchi A, Widmeier E, Lawson JA, Tan W, Hermle T, Warejko JK, Shril S, Airik M, Jobst-Schwan T, Lovric S, Braun DA, Gee HY, Schapiro D, Majmundar AJ, Sadowski CE, Pabst WL, Daga A, van der Ven AT, Schmidt JM, Low BC, Gupta AB, Tripathi BK, Wong J, Campbell K, Metcalfe K, Schanze D, Niihori T, Kaito H, Nozu K, Tsukaguchi H, Tanaka R, Hamahira K, Kobayashi Y, Takizawa T, Funayama R, Nakayama K, Aoki Y, Kumagai N, Iijima K, Fehrenbach H, Kari JA, El Desoky S, Jalalah S, Bogdanovic R, Stajić N, Zappel H, Rakhmetova A, Wassmer SR, Jungraithmayr T, Strehlau J, Kumar AS, Bagga A, Soliman NA, Mane SM, Kaufman L, Lowy DR, Jairajpuri MA, Lifton RP, Pei Y, Zenker M, Kure S, Hildebrandt F.

Nat Commun. 2018 May 17;9(1):1960. doi: 10.1038/s41467-018-04193-w.

4.

Whole Exome Sequencing of Patients with Steroid-Resistant Nephrotic Syndrome.

Warejko JK, Tan W, Daga A, Schapiro D, Lawson JA, Shril S, Lovric S, Ashraf S, Rao J, Hermle T, Jobst-Schwan T, Widmeier E, Majmundar AJ, Schneider R, Gee HY, Schmidt JM, Vivante A, van der Ven AT, Ityel H, Chen J, Sadowski CE, Kohl S, Pabst WL, Nakayama M, Somers MJG, Rodig NM, Daouk G, Baum M, Stein DR, Ferguson MA, Traum AZ, Soliman NA, Kari JA, El Desoky S, Fathy H, Zenker M, Bakkaloglu SA, Müller D, Noyan A, Ozaltin F, Cadnapaphornchai MA, Hashmi S, Hopcian J, Kopp JB, Benador N, Bockenhauer D, Bogdanovic R, Stajić N, Chernin G, Ettenger R, Fehrenbach H, Kemper M, Munarriz RL, Podracka L, Büscher R, Serdaroglu E, Tasic V, Mane S, Lifton RP, Braun DA, Hildebrandt F.

Clin J Am Soc Nephrol. 2018 Jan 6;13(1):53-62. doi: 10.2215/CJN.04120417. Epub 2017 Nov 10.

5.

Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children.

Trautmann A, Schnaidt S, Lipska-Ziętkiewicz BS, Bodria M, Ozaltin F, Emma F, Anarat A, Melk A, Azocar M, Oh J, Saeed B, Gheisari A, Caliskan S, Gellermann J, Higuita LMS, Jankauskiene A, Drozdz D, Mir S, Balat A, Szczepanska M, Paripovic D, Zurowska A, Bogdanovic R, Yilmaz A, Ranchin B, Baskin E, Erdogan O, Remuzzi G, Firszt-Adamczyk A, Kuzma-Mroczkowska E, Litwin M, Murer L, Tkaczyk M, Jardim H, Wasilewska A, Printza N, Fidan K, Simkova E, Borzecka H, Staude H, Hees K, Schaefer F; PodoNet Consortium.

J Am Soc Nephrol. 2017 Oct;28(10):3055-3065. doi: 10.1681/ASN.2016101121. Epub 2017 May 31.

6.

The Child Health Care System of Serbia.

Bogdanović R, Lozanović D, Pejović Milovančević M, Sokal Jovanović L.

J Pediatr. 2016 Oct;177S:S156-S172. doi: 10.1016/j.jpeds.2016.04.053. Epub 2016 Sep 22.

PMID:
27666265
7.

FAT1 mutations cause a glomerulotubular nephropathy.

Gee HY, Sadowski CE, Aggarwal PK, Porath JD, Yakulov TA, Schueler M, Lovric S, Ashraf S, Braun DA, Halbritter J, Fang H, Airik R, Vega-Warner V, Cho KJ, Chan TA, Morris LG, ffrench-Constant C, Allen N, McNeill H, Büscher R, Kyrieleis H, Wallot M, Gaspert A, Kistler T, Milford DV, Saleem MA, Keng WT, Alexander SI, Valentini RP, Licht C, Teh JC, Bogdanovic R, Koziell A, Bierzynska A, Soliman NA, Otto EA, Lifton RP, Holzman LB, Sibinga NE, Walz G, Tufro A, Hildebrandt F.

Nat Commun. 2016 Feb 24;7:10822. doi: 10.1038/ncomms10822.

8.

Mutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndrome.

Braun DA, Sadowski CE, Kohl S, Lovric S, Astrinidis SA, Pabst WL, Gee HY, Ashraf S, Lawson JA, Shril S, Airik M, Tan W, Schapiro D, Rao J, Choi WI, Hermle T, Kemper MJ, Pohl M, Ozaltin F, Konrad M, Bogdanovic R, Büscher R, Helmchen U, Serdaroglu E, Lifton RP, Antonin W, Hildebrandt F.

Nat Genet. 2016 Apr;48(4):457-65. doi: 10.1038/ng.3512. Epub 2016 Feb 15.

9.

Lack of IL7Rα expression in T cells is a hallmark of T-cell immunodeficiency in Schimke immuno-osseous dysplasia (SIOD).

Sanyal M, Morimoto M, Baradaran-Heravi A, Choi K, Kambham N, Jensen K, Dutt S, Dionis-Petersen KY, Liu LX, Felix K, Mayfield C, Dekel B, Bokenkamp A, Fryssira H, Guillen-Navarro E, Lama G, Brugnara M, Lücke T, Olney AH, Hunley TE, Polat AI, Yis U, Bogdanovic R, Mitrovic K, Berry S, Najera L, Najafian B, Gentile M, Nur Semerci C, Tsimaratos M, Lewis DB, Boerkoel CF.

Clin Immunol. 2015 Dec;161(2):355-65. doi: 10.1016/j.clim.2015.10.005. Epub 2015 Oct 21.

PMID:
26499378
10.

Associated extrarenal vascular diseases may complicate the treatment and outcome of renovascular hypertension.

Peco-Antić A, Stajić N, Krstić Z, Bogdanović R, Miloševski-Lomić G, Đukić M, Paripović D.

Acta Paediatr. 2016 Jan;105(1):e35-41. doi: 10.1111/apa.13229. Epub 2015 Nov 4.

PMID:
26437121
11.

Transcriptional and posttranscriptional mechanisms contribute to the dysregulation of elastogenesis in Schimke immuno-osseous dysplasia.

Morimoto M, Wang KJ, Yu Z, Gormley AK, Parham D, Bogdanovic R, Lücke T, Mayfield C, Weksberg R, Hendson G, Boerkoel CF.

Pediatr Res. 2015 Dec;78(6):609-17. doi: 10.1038/pr.2015.156. Epub 2015 Aug 26.

PMID:
26309238
12.

Mutations of the SLIT2-ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract.

Hwang DY, Kohl S, Fan X, Vivante A, Chan S, Dworschak GC, Schulz J, van Eerde AM, Hilger AC, Gee HY, Pennimpede T, Herrmann BG, van de Hoek G, Renkema KY, Schell C, Huber TB, Reutter HM, Soliman NA, Stajic N, Bogdanovic R, Kehinde EO, Lifton RP, Tasic V, Lu W, Hildebrandt F.

Hum Genet. 2015 Aug;134(8):905-16. doi: 10.1007/s00439-015-1570-5. Epub 2015 May 31.

13.

Inhibition of monoacylglycerol lipase mediates a cannabinoid 1-receptor dependent delay of kindling progression in mice.

von Rüden EL, Bogdanovic RM, Wotjak CT, Potschka H.

Neurobiol Dis. 2015 May;77:238-45. doi: 10.1016/j.nbd.2015.03.016. Epub 2015 Mar 18.

PMID:
25796567
14.

Glomerular nestin expression: possible predictor of outcome of focal segmental glomerulosclerosis in children.

Životić M, Bogdanović R, Peco-Antić A, Paripović D, Stajić N, Vještica J, Ćirović S, Trajković G, Marković-Lipkovski J.

Pediatr Nephrol. 2015 Jan;30(1):79-90. doi: 10.1007/s00467-014-2893-5. Epub 2014 Aug 18.

PMID:
25129203
15.

Analysis in conditional cannabinoid 1 receptor-knockout mice reveals neuronal subpopulation-specific effects on epileptogenesis in the kindling paradigm.

von Rüden EL, Jafari M, Bogdanovic RM, Wotjak CT, Potschka H.

Neurobiol Dis. 2015 Jan;73:334-47. doi: 10.1016/j.nbd.2014.08.001. Epub 2014 Aug 11.

PMID:
25123336
16.

(R)-[11C]PK11195 brain uptake as a biomarker of inflammation and antiepileptic drug resistance: evaluation in a rat epilepsy model.

Bogdanović RM, Syvänen S, Michler C, Russmann V, Eriksson J, Windhorst AD, Lammertsma AA, de Lange EC, Voskuyl RA, Potschka H.

Neuropharmacology. 2014 Oct;85:104-12. doi: 10.1016/j.neuropharm.2014.05.002. Epub 2014 May 28.

PMID:
24880085
17.

Congenital thrombocytopenia with nephritis - The first case of MYH9 related disorder in Serbia.

Kuzmanović M, Kunishima S, Putnik J, Stajić N, Paripović A, Bogdanović R.

Vojnosanit Pregl. 2014 Apr;71(4):395-8.

PMID:
24783421
18.

Growth in children with chronic kidney disease: 13 years follow up study.

Salević P, Radović P, Milić N, Bogdanović R, Paripović D, Paripović A, Golubović E, Milosević B, Mulić B, Peco-Antić A.

J Nephrol. 2014 Oct;27(5):537-44. doi: 10.1007/s40620-014-0094-8. Epub 2014 Apr 23.

PMID:
24756972
19.

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.

Kohl S, Hwang DY, Dworschak GC, Hilger AC, Saisawat P, Vivante A, Stajic N, Bogdanovic R, Reutter HM, Kehinde EO, Tasic V, Hildebrandt F.

J Am Soc Nephrol. 2014 Sep;25(9):1917-22. doi: 10.1681/ASN.2013101103. Epub 2014 Apr 3.

20.

Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract.

Hwang DY, Dworschak GC, Kohl S, Saisawat P, Vivante A, Hilger AC, Reutter HM, Soliman NA, Bogdanovic R, Kehinde EO, Tasic V, Hildebrandt F.

Kidney Int. 2014 Jun;85(6):1429-33. doi: 10.1038/ki.2013.508. Epub 2014 Jan 15.

21.

Genotype-phenotype associations in WT1 glomerulopathy.

Lipska BS, Ranchin B, Iatropoulos P, Gellermann J, Melk A, Ozaltin F, Caridi G, Seeman T, Tory K, Jankauskiene A, Zurowska A, Szczepanska M, Wasilewska A, Harambat J, Trautmann A, Peco-Antic A, Borzecka H, Moczulska A, Saeed B, Bogdanovic R, Kalyoncu M, Simkova E, Erdogan O, Vrljicak K, Teixeira A, Azocar M, Schaefer F; PodoNet Consortium.

Kidney Int. 2014 May;85(5):1169-78. doi: 10.1038/ki.2013.519. Epub 2014 Jan 8.

22.

Whole-exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association.

Saisawat P, Kohl S, Hilger AC, Hwang DY, Yung Gee H, Dworschak GC, Tasic V, Pennimpede T, Natarajan S, Sperry E, Matassa DS, Stajić N, Bogdanovic R, de Blaauw I, Marcelis CL, Wijers CH, Bartels E, Schmiedeke E, Schmidt D, Märzheuser S, Grasshoff-Derr S, Holland-Cunz S, Ludwig M, Nöthen MM, Draaken M, Brosens E, Heij H, Tibboel D, Herrmann BG, Solomon BD, de Klein A, van Rooij IA, Esposito F, Reutter HM, Hildebrandt F.

Kidney Int. 2014 Jun;85(6):1310-7. doi: 10.1038/ki.2013.417. Epub 2013 Oct 23.

23.

Molecular characterization of cystinuria in south-eastern European countries.

Popovska-Jankovic K, Tasic V, Bogdanovic R, Miljkovic P, Golubovic E, Soylu A, Saraga M, Pavicevic S, Baskin E, Akil I, Gregoric A, Lilova M, Topaloglu R, Sukarova Stefanovska E, Plaseska-Karanfilska D.

Urolithiasis. 2013 Feb;41(1):21-30. doi: 10.1007/s00240-012-0531-x. Epub 2012 Dec 27.

PMID:
23532419
24.

Pulmonary renal syndrome in a child with coexistence of anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane disease: case report and literature review.

Bogdanović R, Minić P, Marković-Lipkovski J, Stajić N, Savić N, Rodić M.

BMC Nephrol. 2013 Mar 22;14:66. doi: 10.1186/1471-2369-14-66. Review.

25.

Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

Lipska BS, Iatropoulos P, Maranta R, Caridi G, Ozaltin F, Anarat A, Balat A, Gellermann J, Trautmann A, Erdogan O, Saeed B, Emre S, Bogdanovic R, Azocar M, Balasz-Chmielewska I, Benetti E, Caliskan S, Mir S, Melk A, Ertan P, Baskin E, Jardim H, Davitaia T, Wasilewska A, Drozdz D, Szczepanska M, Jankauskiene A, Higuita LM, Ardissino G, Ozkaya O, Kuzma-Mroczkowska E, Soylemezoglu O, Ranchin B, Medynska A, Tkaczyk M, Peco-Antic A, Akil I, Jarmolinski T, Firszt-Adamczyk A, Dusek J, Simonetti GD, Gok F, Gheissari A, Emma F, Krmar RT, Fischbach M, Printza N, Simkova E, Mele C, Ghiggeri GM, Schaefer F; PodoNet Consortium.

Kidney Int. 2013 Jul;84(1):206-13. doi: 10.1038/ki.2013.93. Epub 2013 Mar 20.

26.

Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney Disease.

Schmidts M, Frank V, Eisenberger T, Al Turki S, Bizet AA, Antony D, Rix S, Decker C, Bachmann N, Bald M, Vinke T, Toenshoff B, Di Donato N, Neuhann T, Hartley JL, Maher ER, Bogdanović R, Peco-Antić A, Mache C, Hurles ME, Joksić I, Guć-Šćekić M, Dobricic J, Brankovic-Magic M, Bolz HJ, Pazour GJ, Beales PL, Scambler PJ, Saunier S, Mitchison HM, Bergmann C.

Hum Mutat. 2013 May;34(5):714-24. doi: 10.1002/humu.22294.

27.

Granulomatosis with polyangiitis (Wegener's granulomatosis) in children: report of three cases with cutaneous manifestations and literature review.

Gajic-Veljic M, Nikolic M, Peco-Antic A, Bogdanovic R, Andrejevic S, Bonaci-Nikolic B.

Pediatr Dermatol. 2013 Jul-Aug;30(4):e37-42. doi: 10.1111/pde.12034. Epub 2012 Nov 12. Review.

PMID:
23145989
28.

Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?

Morimoto M, Yu Z, Stenzel P, Clewing JM, Najafian B, Mayfield C, Hendson G, Weinkauf JG, Gormley AK, Parham DM, Ponniah U, André JL, Asakura Y, Basiratnia M, Bogdanović R, Bokenkamp A, Bonneau D, Buck A, Charrow J, Cochat P, Cordeiro I, Deschenes G, Fenkçi MS, Frange P, Fründ S, Fryssira H, Guillen-Navarro E, Keller K, Kirmani S, Kobelka C, Lamfers P, Levtchenko E, Lewis DB, Massella L, McLeod DR, Milford DV, Nobili F, Saraiva JM, Semerci CN, Shoemaker L, Stajić N, Stein A, Taha D, Wand D, Zonana J, Lücke T, Boerkoel CF.

Orphanet J Rare Dis. 2012 Sep 22;7:70. doi: 10.1186/1750-1172-7-70.

29.

Dental abnormalities in Schimke immuno-osseous dysplasia.

Morimoto M, Kérourédan O, Gendronneau M, Shuen C, Baradaran-Heravi A, Asakura Y, Basiratnia M, Bogdanovic R, Bonneau D, Buck A, Charrow J, Cochat P, Dehaai KA, Fenkçi MS, Frange P, Fründ S, Fryssira H, Keller K, Kirmani S, Kobelka C, Kohler K, Lewis DB, Massella L, McLeod DR, Milford DV, Nobili F, Olney AH, Semerci CN, Stajic N, Stein A, Taque S, Zonana J, Lücke T, Hendson G, Bonnaure-Mallet M, Boerkoel CF.

J Dent Res. 2012 Jul;91(7 Suppl):29S-37S.

30.

[Chronic kidney disease during a 12-year period at tertiary health institution].

Paripović A, Stajić N, Putnik J, Bogdanović R.

Srp Arh Celok Lek. 2012 May-Jun;140(5-6):313-20. Serbian.

31.

Long-term genetic fate mapping of adult generated neurons in a mouse temporal lobe epilepsy model.

Jafari M, Soerensen J, Bogdanović RM, Dimou L, Götz M, Potschka H.

Neurobiol Dis. 2012 Dec;48(3):454-63. doi: 10.1016/j.nbd.2012.06.014. Epub 2012 Jun 30.

PMID:
22750527
32.

Atypical presentation of cystic fibrosis--obese adolescent with hypertension and pseudo-Bartter's syndrome.

Sovtić A, Minić P, Bogdanović R, Stajić N, Rodić M, Marković-Sovtić G.

Vojnosanit Pregl. 2012 Apr;69(4):367-9.

PMID:
22624431
33.

Renal involvement in primary Sjogren syndrome of childhood: case report and literature review.

Bogdanović R, Basta-Jovanović G, Putnik J, Stajić N, Paripović A.

Mod Rheumatol. 2013 Jan;23(1):182-9. doi: 10.1007/s10165-012-0633-x. Epub 2012 Apr 7. Review.

PMID:
22484709
34.

Epidemiology of chronic kidney disease in children in Serbia.

Peco-Antic A, Bogdanovic R, Paripovic D, Paripovic A, Kocev N, Golubovic E, Milosevic B; Serbian Pediatric Registry of Chronic Kidney Disease (SPRECKID).

Nephrol Dial Transplant. 2012 May;27(5):1978-84. doi: 10.1093/ndt/gfr556. Epub 2011 Nov 3.

PMID:
22058136
35.

Infantile nephropathic cystinosis.

Peco-Antić A, Kostić M, Bogdanović R, Spasojević B, Djordjević M, Paripović D, Kovacević D.

Srp Arh Celok Lek. 2011 Jul-Aug;139(7-8):486-90.

36.

Liddle syndrome in a Serbian family and literature review of underlying mutations.

Bogdanović R, Kuburović V, Stajić N, Mughal SS, Hilger A, Ninić S, Prijić S, Ludwig M.

Eur J Pediatr. 2012 Mar;171(3):471-8. doi: 10.1007/s00431-011-1581-8. Epub 2011 Sep 29. Review.

PMID:
21956615
37.

Effect of growth hormone replacement therapy in a boy with Dent's disease: a case report.

Samardzic M, Pavicevic S, Ludwig M, Bogdanovic R.

J Med Case Rep. 2011 Aug 22;5:400. doi: 10.1186/1752-1947-5-400.

38.

[Transient pseudohypoaldosteronism].

Stajić N, Putnik J, Paripović A, Bogdanović R.

Srp Arh Celok Lek. 2011 Jan-Feb;139(1-2):37-43. Serbian.

39.

Diagnostic role of initial renal cortical scintigraphy in children with the first episode of acute pyelonephritis.

Jaksic E, Bogdanovic R, Artiko V, Saranovic DS, Petrasinovic Z, Petrovic M, Bojic L, Pavlovic S, Paripovic A, Antonovic O, Lezaic VD, Saranovic D, Petrovic N, Obradovic V.

Ann Nucl Med. 2011 Jan;25(1):37-43. doi: 10.1007/s12149-010-0431-5. Epub 2010 Nov 16.

PMID:
21080122
40.

A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency.

Bogdanović R, Draaken M, Toromanović A, Dordević M, Stajić N, Ludwig M.

Pediatr Nephrol. 2010 Nov;25(11):2363-8. doi: 10.1007/s00467-010-1615-x. Epub 2010 Aug 1.

PMID:
20680351
41.

Schimke immunoosseous dysplasia: defining skeletal features.

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.

Eur J Pediatr. 2010 Jul;169(7):801-11. doi: 10.1007/s00431-009-1115-9. Epub 2009 Dec 15.

42.

Transient type 1 pseudo-hypoaldosteronism: report on an eight-patient series and literature review.

Bogdanović R, Stajić N, Putnik J, Paripović A.

Pediatr Nephrol. 2009 Nov;24(11):2167-75. doi: 10.1007/s00467-009-1285-8. Review.

PMID:
19714368
43.

Henoch-Schönlein purpura nephritis in children: risk factors, prevention and treatment.

Bogdanović R.

Acta Paediatr. 2009 Dec;98(12):1882-9. doi: 10.1111/j.1651-2227.2009.01445.x. Epub 2009 Jul 24. Review.

PMID:
19650836
44.

[Dent's disease].

Pavićević S, Bogdanović R, Ludwig M, Samardzić M.

Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:312-5. Serbian.

45.

[Congenital nephrotic syndrome].

Stajić N, Putnik J, Paripović A, Djurić S, Bogdanović R.

Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:307-11. Serbian.

46.

[The significance of Goodpasture antigen in hereditary nephritis].

Basta-Jovanović G, Radojević-Skodrić S, Jovanović M, Bogdanović L, Bogdanović R, Lezaić V, Nesić V, Dikman S.

Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:282-6. Serbian.

47.

[Alport's syndrome and benign familial haematuria: light and electron microscopic studies of the kidney].

Dimitrijević J, Todorović V, Aleksić A, Jovanović D, Pilcević D, Vignjević S, Mićić S, Jovanović D, Pilcević D, Kovacević Z, Hrvacević R, Maksić D, Brajusković G, Savić V, Bogdanović R.

Srp Arh Celok Lek. 2008 Dec;136 Suppl 4:275-81. Serbian.

48.

Missense mutations in EYA1 and TCF2 are a rare cause of urinary tract malformations.

Hoskins BE, Cramer CH 2nd, Tasic V, Kehinde EO, Ashraf S, Bogdanovic R, Hoefele J, Pohl M, Hildebrandt F.

Nephrol Dial Transplant. 2008 Feb;23(2):777-9. Epub 2007 Dec 8. No abstract available.

PMID:
18065799
49.

Diabetic nephropathy in children and adolescents.

Bogdanović R.

Pediatr Nephrol. 2008 Apr;23(4):507-25. Epub 2007 Oct 17. Review.

PMID:
17940807
50.

Sonographic assessment of normal kidney dimensions in the first year of life--a study of 992 healthy infants.

Vujic A, Kosutic J, Bogdanovic R, Prijic S, Milicic B, Igrutinovic Z.

Pediatr Nephrol. 2007 Aug;22(8):1143-50. Epub 2007 Mar 31.

PMID:
17401585

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