R. Bogdanović

发表

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

I. V. van Rooij, D. Tibboel, V. Tasic, 2013, Kidney international.

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

V. Tasic, F. Hildebrandt, A. Vivante, 2014, Kidney international.

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

S. Mane, R. Lifton, V. Tasic, 2018, Clinical journal of the American Society of Nephrology : CJASN.

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

N. Stajić, R. Bogdanović, P. Minić, 2013, BMC Nephrology.

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

N. Stajić, R. Bogdanović, J. Putnik, 2009, Pediatric Nephrology.

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

A. Anarat, G. Remuzzi, M. Litwin, 2017, Journal of the American Society of Nephrology : JASN.

Genotype-phenotype associations in WT1 glomerulopathy.

K. Tory, G. Caridi, P. Iatropoulos, 2014, Kidney international.

Mutations of the SLIT 2-ROBO 2 pathway genes SLIT 2 and SRGAP 1 Confer Risk for Congenital Anomalies of the Kidney and Urinary Tract

Soliman, Weining Lu, V. Tasic, 2015 .

Epidemiology of chronic kidney disease in children in Serbia.

N. Kocev, R. Bogdanović, A. Paripović, 2012, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

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

N. Milic, R. Bogdanović, A. Paripović, 2014, Journal of Nephrology.

Association of migraine‐like headaches with Schimke immuno‐osseous dysplasia

I. Kaitila, C. Boerkoel, D. Milford, 2005, American journal of medical genetics. Part A.

Frasier syndrome diagnosed in a 4-year-old girl

R. Bogdanović, V. Stojanović, M. Kostić, 2012 .

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

J. Charrow, C. Boerkoel, D. Lewis, 2012, Orphanet Journal of Rare Diseases.

Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literature

R. Weksberg, D. Geary, I. Kaitila, 2000, European Journal of Pediatrics.

Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

A. Anarat, G. Ardissino, G. Ghiggeri, 2013, Kidney international.

Evaluation of carotid intima media thickness in children with idiopathic nephrotic syndrome.

N. Stajić, R. Bogdanović, J. Putnik, 2020, Nephrologie & therapeutique.

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

N. Stajić, R. Bogdanović, J. Putnik, 2012, Srpski arhiv za celokupno lekarstvo.

Five Novel Mutations in Cystinuria Genes SLC3A1 and SLC7A9

V. Tasic, K. Popovska-Jankovic, D. Plaseska-Karanfilska, 2009 .

Mutant chromatin remodeling protein SMARCAL1 causes Schimke immuno-osseous dysplasia

Rosanna Weksberg, Pawel Stankiewicz, Hiroshi Takashima, 2002, Nature Genetics.

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

C. Boerkoel, D. Lewis, A. Baradaran‐Heravi, 2015, Clinical immunology.

Dental Abnormalities in Schimke Immuno-osseous Dysplasia

J. Charrow, C. Boerkoel, D. Lewis, 2012, Journal of dental research.

Schimke immunoosseous dysplasia: suggestions of genetic diversity

C. Cancrini, C. Boerkoel, J. Ehrich, 2007, Human mutation.

[Schimke immuno-osseous dysplasia].

G. Vlahović, N. Stajić, R. Bogdanović, 2001, Srpski arhiv za celokupno lekarstvo.

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

N. Stajić, R. Bogdanović, J. Putnik, 2013, Modern rheumatology.

Genotype-phenotype associations in WT1

P. Iatropoulos, M. Szczepańska, B. Ranchin, 2014 .

Mutations in the Wilms' Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9

F. Hildebrandt, B. Hoskins, B. Hinkes, 2006, Pediatric Research.

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

V. Tasic, F. Hildebrandt, B. Hoskins, 2007, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

[Congenital nephrotic syndrome].

N. Stajić, R. Bogdanović, J. Putnik, 2008, Srpski arhiv za celokupno lekarstvo.

Schimke immunoosseous dysplasia: defining skeletal features

C. Boerkoel, D. Bonneau, S. Smithson, 2009, European Journal of Pediatrics.

Infantile nephropathic cystinosis.

R. Bogdanović, A. Peco‐Antić, D. Paripovic, 2011, Srpski arhiv za celokupno lekarstvo.

Combined NGS Approaches Identify Mutations in the Intraflagellar Transport Gene IFT140 in Skeletal Ciliopathies with Early Progressive Kidney Disease

M. Hurles, P. Scambler, T. Neuhann, 2013, Human mutation.

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

N. Stajić, R. Bogdanović, S. Kunishima, 2014, Vojnosanitetski pregled.

FAT1 mutations cause a glomerulotubular nephropathy

T. Chan, R. Lifton, D. Milford, 2016, Nature Communications.