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European Journal of Rheumatology|May 13, 2022
Next-Generation Sequencing Analysis of MVK, NLRP3, TNFRSF1A, and PSTPIP1 Genes in Patients without MEFV Gene Variation and Genotype-Phenotype CorrelationGamze Vuran, Afig BerdeliBiochemical Genetics|April 25, 2009
Prevalence of the angiotensin I converting enzyme gene insertion/deletion polymorphism in a healthy Turkish populationAfig Berdeli, F Sirri CamISRN Rheumatology|April 7, 2012
Complement-4 deficiency in a child with systemic lupus erythematosus presenting with standard treatment-resistant severe skin lesionBetul Sozeri, Sevgi Mir, Afig BerdeliIranian Journal of Kidney Diseases|November 10, 2019
Genetics and outcome of atypical hemolytic-uremic syndrome in Turkish children: a retrospective study between 2010 and 2017, a single-center experienceSeçil Conkar, Sevgi Mir, Afig BerdeliBosnian Journal of Basic Medical Sciences|July 1, 2016
NOD2/CARD15 gene mutations in patients with gouty arthritisAhmet Karaarslan, Senol Kobak, Afig BerdeliGene|March 31, 2022
MEFV gene allele frequency and genotype distribution in 3230 patients' analyses by next generation sequencing methodsBerkay Kırnaz, Yüksel Gezgin, Afig BerdeliEuropean Journal of Rheumatology|August 1, 2019
Treatment of familial mediterranean fever with canakinumab in patients who are unresponsive to colchicineAfig Berdeli, Özgür Şenol, Gamze TalayPediatric Transplantation|September 24, 2005
Hypertension and ace gene insertion/deletion polymorphism in pediatric renal transplant patientsErkin Serdaroglu, Sevgi Mir, Afig BerdeliMolecular Biology Reports|March 16, 2022
Screening of OTULIN gene mutation with targeted next generation sequencing in Turkish populations and in silico analysis of these mutationsYüksel Gezgin, Berkay Kırnaz, Afig BerdeliPediatric Rheumatology Online Journal|December 11, 2025
Novel HCK-associated mutation causing autoinflammatory disorder with pulmonary manifestations in a pediatric patientAfig Berdeli, Shams Ismayilova, Nida GürbüzPageof 14