Emine Korkmaz
Ankara, Turkey
Last Updated: 09/26/2026
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Found 14 publications
Hemolytic uremic syndrome and IgA nephropathy in a child: Coincidence or not?
Journal: The Turkish journal of pediatrics
Published: August 14, 2018
Atypical Hemolytic Uremic Syndrome in Children Aged <2 Years.
Journal: Nephron
Published: September 27, 2017
Epidermolysis Bullosa with Pyloric Atresia and Aplasia Cutis in a Newborn Due to Homozygous Mutation in ITGB4.
Journal: Fetal and pediatric pathology
Published: May 31, 2017
Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment.
Journal: Pediatric nephrology (Berlin, Germany)
Published: October 01, 2016
First-Line, Early and Long-Term Eculizumab Therapy in Atypical Hemolytic Uremic Syndrome: A Case Series in Pediatric Patients.
Journal: Paediatric drugs
Published: September 21, 2016
Turkish pediatric atypical hemolytic uremic syndrome registry: initial analysis of 146 patients.
Journal: BMC nephrology
Published: September 21, 2016
Familial Mediterranean fever patients homozygous for E148Q variant may have milder disease.
Journal: International journal of rheumatic diseases
Published: July 27, 2016
ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS.
Journal: Journal of the American Society of Nephrology : JASN
Published: December 20, 2014
Genetic abnormalities and prognosis in patients with congenital and infantile nephrotic syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: October 16, 2014
Mutations in ANKS6 cause a nephronophthisis-like phenotype with ESRD.
Journal: Journal of the American Society of Nephrology : JASN
Published: March 11, 2014
Mutations in EMP2 cause childhood-onset nephrotic syndrome.
Journal: American journal of human genetics
Published: January 06, 2014
A novel CFHR5 mutation associated with C3 glomerulonephritis in a Turkish girl.
Journal: Journal of nephrology
Published: July 17, 2013
Last Updated: 09/26/2026