Maria U. Daniel
Warsaw, MZ, Poland
Last Updated: 09/26/2026
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Found 11 publications
Familial hyponatremia conditioned by the R137C mutation with constitutive activation of the vasopressin receptor.
Journal: Journal of applied genetics
Published: November 30, 2024
Lactobacillus rhamnosus PL1 and Lactobacillus plantarum PM1 versus Placebo as Prophylaxis for Recurrence of Urinary Tract Infections in Children.
Journal: Microorganisms
Published: April 10, 2024
The usefulness of urinary netrin-1 determination as an early marker of acute kidney injury in children after cardiac surgery.
Journal: Archives of medical science : AMS
Published: March 03, 2024
Epidemiology and Risk Factors of UTIs in Children-A Single-Center Observation.
Journal: Journal of personalized medicine
Published: November 02, 2022
Compound Haplotype Variants in CFH and CD46 Genes Determine Clinical Outcome of Atypical Hemolytic Uremic Syndrome (aHUS)-A Series of Cases from a Single Family.
Journal: Journal of personalized medicine
Published: March 26, 2021
Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35.
Journal: American journal of medical genetics. Part A
Published: March 30, 2020
Is copeptin a reliable biomarker of primary monosymptomatic nocturnal enuresis?
Journal: Central-European journal of immunology
Published: August 04, 2018
7-day compared with 10-day antibiotic treatment for febrile urinary tract infections in children: protocol of a randomised controlled trial.
Journal: BMJ open
Published: March 04, 2018
Diagnostic difficulties in a patient with paroxysmal cold haemoglobinuria and acute kidney injury.
Journal: Central-European journal of immunology
Published: December 30, 2016
Hypertensive crisis in children and adolescents
Journal: Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego
Published: February 05, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026