3 results match your criteria: "University Clinic for Children's Disease[Affiliation]"
Differentinating between non-transfusion dependant β-thalassemia and iron deficinecy anemia in children using ROC and logistic regression analysis: two novel discrimination indices designed for pediatric patients.
Front Pediatr
January 2024
School of Medicine, University of Zagreb, Zagreb, Croatia.
Introduction: This cross-sectional study enrolled a group of 271 children with microcytic anemia in order to test the performance of 41 single and 2 composite formulas andindices in distinguishing between β-thalassemia (β-thal) and iron deficiency anemia (IDA) in the pediatric population.
Methods: Optimal pediatric cut-off values from the previously published formulas and indices were generated using ROC analysis. Logistic regression in R using generalized linear models (GLM) generated two new indices.
A novel mutation in SLC39A7 identified in a patient with autosomal recessive agammaglobulinemia: The impact of the J Project.
Pediatr Allergy Immunol
June 2022
Primary Immunodeficiency Clinical Unit and Laboratory, Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Anti-Factor H Antibody-Associated Atypical Hemolytic Uremic Syndrome: A Case Report.
Pril (Makedon Akad Nauk Umet Odd Med Nauki)
October 2021
University Clinic for Children's Disease, Department of Nephrology, Medical Faculty, Skopje, N Macedonia.
: Atypical hemolytic uremic syndrome (aHUS) is a rare form of thrombotic microangiopathy, caused by dysregulation of the complement alternative pathway. Deletion of the complement factor H-related genes, CFHR1 and CFHR3, together with the presence of CFH autoantibodies are reported in aHUS patients, representing 10% of cases of patients with aHUS. : We report here on a case of 4-year-old girl with anti-CFH antibody-associated aHUS.
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