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Agnieszka Szmigielska
Medical University of Warsaw
UrologyHydronephrosisDiabetes mellitusMedicineUrinary system
58Publications
6H-index
169Citations
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Publications 57
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#1Miguel VerbitskyH-Index: 21
#2Rik WestlandH-Index: 15
Last. Simone Sanna-CherchiH-Index: 29
view all 90 authors...
In the version of this article initially published, affiliation 38 incorrectly read “ICNU-Nephrology and Urology Department, Barcelona, Spain”; “Renal Division, Hospital Clinic, IDIBAPS, University of Barcelona, Barcelona, Spain” is the correct affiliation. The error has been corrected in the HTML and PDF versions of the article.
#1Miguel Verbitsky (Columbia University)H-Index: 21
#2Rik Westland (Columbia University)H-Index: 15
Last. Simone Sanna-Cherchi (Columbia University)H-Index: 29
view all 90 authors...
In the version of this article initially published, affiliation 38 incorrectly read “ICNU-Nephrology and Urology Department, Barcelona, Spain”; “Renal Division, Hospital Clinic, IDIBAPS, University of Barcelona, Barcelona, Spain” is the correct affiliation. The error has been corrected in the HTML and PDF versions of the article.
Source
#1Miguel Verbitsky (Columbia University)H-Index: 21
#2Rik Westland (Columbia University)H-Index: 15
Last. Simone Sanna-Cherchi (Columbia University)H-Index: 29
view all 90 authors...
Congenital anomalies of the kidney and urinary tract (CAKUT) are a major cause of pediatric kidney failure. We performed a genome-wide analysis of copy number variants (CNVs) in 2,824 cases and 21,498 controls. Affected individuals carried a significant burden of rare exonic (that is, affecting coding regions) CNVs and were enriched for known genomic disorders (GD). Kidney anomaly (KA) cases were most enriched for exonic CNVs, encompassing GD-CNVs and novel deletions; obstructive uropathy (OU) h...
8 CitationsSource
#1Grażyna Krzemień (Medical University of Warsaw)H-Index: 6
#2Agnieszka Turczyn (Medical University of Warsaw)H-Index: 3
Last. Agnieszka Szmigielska (Medical University of Warsaw)H-Index: 6
view all 6 authors...
Introduction: Kidney injury molecule-1 (KIM-1) is an important diagnostic and prognostic marker in acute kidney injury and chronic kidney disease of various aetiologies. The aim of the study was to evaluate the usefulness of serum KIM-1 (sKIM-1) and urine KIM-1 (uKIM-1) for predicting febrile and non-febrile urinary tract infection (UTI) in infants. Material and methods: A prospective study included 101 children divided into three groups: febrile UTI 49 children, non-febrile UTI 22 children, and...
1 CitationsSource
Introduction: Fever and elevated inflammatory markers have been used for diagnosis of acute pyelonephritis (APN) in infants with urinary tract infection (UTI).The aim of the study was to compare the usefulness of serum neutrophil gelatinase-associated lipocalin (sNGAL) with inflammatory markers for predicting APN in infants with UTI. Material and methods: The prospective study included 46 infants with a first episode of UTI, divided into two groups (APN 23, lower UTI 23), according to the DMSA s...
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#1Grażyna Krzemień (Medical University of Warsaw)H-Index: 6
#2Małgorzata Pańczyk-Tomaszewska (Medical University of Warsaw)H-Index: 7
Last. Agnieszka Szmigielska (Medical University of Warsaw)H-Index: 6
view all 5 authors...
Introduction: We assessed whether two urinary biomarkers of acute kidney injury, neutrophil gelatinase associated lipocalin (uNGAL) and kidney injury molecule-1 (uKIM-1), can be useful for predicting acute pyelonephritis (APN) in children aged 1-24 months with the first febrile urinary tract infection (UTI). Material and methods: A prospective study included 54 children divided into two groups (24 with APN, 30 with lower UTI), according to the dimercaptosuccinic acid (DMSA) renal scintigraphy re...
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The incidence of urolithiasis in infants is unknown. The aim of this study was to investigate clinical characteristics, nutrition, calcium, phosphate, 25-hydroxyvitamin D (25(OH)D), alkaline phosphate, and parathyroid hormone in infants with urolithiasis. There were 32 infants (23 boys and 9 girls) of the mean age of 6.4 ± 3.7 months (range 2–12 months), with diagnosis of urolithiasis enrolled into the study. Boys were younger than girls (5.3 vs. 9.1 months, respectively; p < 0.05). The infants ...
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#1Agnieszka Szmigielska (Medical University of Warsaw)H-Index: 6
#2Grażyna Krzemień (Medical University of Warsaw)H-Index: 6
Last. Stanisław WarchołH-Index: 4
view all 5 authors...
Renal agenesis occurs in pediatric population with the incidence 1:500- 2000 children. It is more often diagnosed in boys and on the left side of the body. Renal agenesis may be isolated or it may be a part of complex malformation syndrome. Megacalycosis is a very rare anomaly of urinary tract associated with abnormal structure of the kidney pyramids.The aim of the study was to present for the first time in the medical literature the case of a girl with unilateral renal agenesis and megacalycosi...
#1Grażyna Krzemień (Medical University of Warsaw)H-Index: 6
#2Jarosław Sołtyski (Medical University of Warsaw)
Last. Aleksandra Jakimów-Kostrzewa (Medical University of Warsaw)H-Index: 1
view all 6 authors...
Hydronephrosis in children is most often due to an intrinsic ureteropelvic junction obstruction or by compression on ureter by accessory renal artery coming from the aorta to the lower pole of the kidney. AIM: The aim of study was to present a case with a late onset of hydronephrosis caused by accessory renal artery. CASE REPORT: 5-year old boy with a mild pyelectasia during first 10 months of age was admitted to hospital because of abdominal pain and vomiting. Abdominal ultrasound revealed a ma...
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