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27 results on '"Krzemień G"'

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1. Antibiotic Prophylaxis in Infants with Grade III, IV, or V Vesicoureteral Reflux.

2. Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.

3. Serum and urine periostin and cytokeratin-18 in children with congenital obstructive nephropathy.

4. The Usefulness of Urinary Periostin, Cytokeratin-18, and Endoglin for Diagnosing Renal Fibrosis in Children with Congenital Obstructive Nephropathy.

5. Urinary vanin-1 for predicting acute pyelonephritis in young children with urinary tract infection: a pilot study.

6. Clinical profile of neonates with hypernatremic dehydration in a nephrology clinic.

7. Massive thrombosis in an infant with suspected nephrocalcinosis: case report and literature review.

8. Serum neutrophil gelatinase-associated lipocalin for predicting acute pyelonephritis in infants with urinary tract infection.

9. Diagnostic accuracy of urine neutrophil gelatinase-associated lipocalin and urine kidney injury molecule-1 as predictors of acute pyelonephritis in young children with febrile urinary tract infection.

10. Vitamin D and Calcium Homeostasis in Infants with Urolithiasis.

11. Prognostic value of serum and urine kidney injury molecule-1 in infants with urinary tract infection.

12. [Dodatkowa tętnica nerkowa przyczyną skrajnego wodonercza u 5-letniego chłopca].

13. [Congenital megacalycosis in a girl with unilateral renal agenesis].

14. Pyonephrosis as the first symptom of congenital hydronephrosis in a 6-year old girl.

15. [High ureteral insertion as the cause of extreme hydronephrosis in a 5-year-old child with horseshoe kidney].

16. Neutrophil Gelatinase-Associated Lipocalin: A Biomarker for Early Diagnosis of Urinary Tract Infections in Infants.

17. Long-term follow up of a boy with unilateral autosomal dominant polycystic kidney disease and contralateral renal agenesis.

18. Endoscopic correction of vesicoureteral reflux in children using polyacrylate-polyalcohol copolymer (Vantris): 5-years of prospective follow-up.

19. [Sterile leukocyturia - difficult diagnostic problem in children].

20. Polydactyly and obesity - the clinical manifestation of ciliopathy: a boy with Bardet-Biedl syndrome.

21. Extreme hydronephrosis due to uretropelvic junction obstruction in infant (case report).

22. Urine interleukin-6, interleukin-8 and transforming growth factor β1 in infants with urinary tract infection and asymptomatic bacteriuria.

23. [Renal staghorn calculi in small children - presentation of two cases].

24. VIT. B12 DEFICIENCY IN CHILDREN (IMERSLUND-GRÄSBECK SYNDROME IN TWO PAIRS OF SIBLINGS).

25. Ceftriaxone-associated acute gallbladder enlargement - an unexpected diagnosis in the child with urinary tract infection.

26. Rare renal ectopia in children - intrathoracic ectopic kidney.

27. Calyceal diverticulum of the kidney - diagnostic imaging dilemma in pediatric patients - case report.

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