All Stories

  1. A 9.5-year-old boy with recurrent neurological manifestations and severe hypertension, treated initially for polyarteritis nodosa, was subsequently diagnosed with adenosine deaminase type 2 deficiency (DADA2) which responded to anti-TNF-α

    Article • Paediatrics and International Child Health, January 2019, Taylor & Francis

    OZGUR KASAPCOPUR, Eda Tahir Turanli, Professor Ozgur KASAPCOPUR

  2. Hepatitis A virus vaccination in childhood-onset systemic lupus erythematosus

    Article • Lupus, December 2018, SAGE Publications

    OZGUR KASAPCOPUR, Professor Ozgur KASAPCOPUR

  3. Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome

    Article • Molecular Genetics & Genomic Medicine, February 2018, Wiley

    OZGUR KASAPCOPUR, Professor Ozgur KASAPCOPUR

  4. Juvenile systemic lupus erythematosus in Turkey: demographic, clinical and laboratory features with disease activity and outcome

    Article • Lupus, December 2017, SAGE Publications

    OZGUR KASAPCOPUR, Professor Ozgur KASAPCOPUR

  5. Deficiency of Complement 1r Subcomponent in Early-Onset Systemic Lupus Erythematosus: The Role of Disease-Modifying Alleles in a Monogenic Disease

    Article • Arthritis & Rheumatology, July 2017, Wiley

    OZGUR KASAPCOPUR, Professor Ozgur KASAPCOPUR

  6. Pentraxin-3 levels are associated with vasculitis and disease activity in childhood-onset systemic lupus erythematosus

    Article • Lupus, March 2017, SAGE Publications

    OZGUR KASAPCOPUR, Professor Ozgur KASAPCOPUR, Professor Hafize Uzun