Mustafa Yavuz Köker

Hematologically important mutations: X-linked chronic granulomatous disease (third update)

Dirk Roos, Douglas B. Kuhns, Anne Maddalena et al. · Blood Cells Molecules and Diseases · 2010 · 198 citations · Full text

Granulocyte, Genetic Disorder, Hematology +5

Human NLRP3 inflammasome activation is Nox1-4 independent

Robin van Bruggen, Mustafa Yavuz Köker, Machiel H. Jansen et al. · Blood · 2010 · 197 citations · Full text

Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients

Mustafa Yavuz Köker, Yıldız Çamcıoğlu, Karin van Leeuwen et al. · Journal of Allergy and Clinical Immunology · 2013 · 177 citations

Turkish Patients, Autoimmune Disease, Chronic Granulomatous Disease +10

Chronic granulomatous disease caused by mutations other than the common GT deletion in<i>NCF1</i>, the gene encoding the p47^phoxcomponent of the phagocyte NADPH oxidase

Dirk Roos, Martin de Boer, Mustafa Yavuz Köker et al. · Human Mutation · 2006 · 61 citations

Family Members, Genetics, Immunodeficiencies +24

Predictive values of neutrophil CD64 expression compared with interleukin‐6 and C‐reactive protein in early diagnosis of neonatal sepsis

Dílek Díllí, Ş. Suna Ogˇuz, U. Dilmen et al. · Journal of Clinical Laboratory Analysis · 2010 · 57 citations · Full text