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Page 1
Familial mediterranean Fever: diagnosing as early as 3 months of age.
Keskindemirci G, Aktay Ayaz N, Aldemir E, Aydoğmuş C, Aydoğan G, Kavuncuoğlu S. Keskindemirci G, et al. Case Rep Pediatr. 2014;2014:296479. doi: 10.1155/2014/296479. Epub 2014 Mar 27. Case Rep Pediatr. 2014. PMID: 24800095 Free PMC article.
HAX-1 deficiency: Characteristics of five cases including an asymptomatic patient.
Aydogmus C, Cipe F, Tas M, Akinel A, Öner Ö, Keskindemirci G, Bornaun H, Kutluk G, Hocaoglu AB. Aydogmus C, et al. Among authors: keskindemirci g. Asian Pac J Allergy Immunol. 2016 Mar;34(1):73-6. doi: 10.12932/AP0618.34.1.2016. Asian Pac J Allergy Immunol. 2016. PMID: 26994629 Free article.
Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations.
Çakan M, Aktay-Ayaz N, Keskindemirci G, Karadağ ŞG. Çakan M, et al. Among authors: keskindemirci g. Turk J Pediatr. 2017;59(4):467-470. doi: 10.24953/turkjped.2017.04.015. Turk J Pediatr. 2017. PMID: 29624229 Free article.
Cakan M, Aktay-Ayaz N, Keskindemirci G, Karadag SG. Two cases of periodic fever syndrome with coexistent mevalonate kinase and Mediterranean fever gene mutations. ...
Cakan M, Aktay-Ayaz N, Keskindemirci G, Karadag SG. Two cases of periodic fever syndrome with coexistent mevalonate kinase and …
41 results